JP5823446B2 - N.meningitidis血清型b外膜タンパク質を含む外膜小胞(omv)ワクチン - Google Patents
N.meningitidis血清型b外膜タンパク質を含む外膜小胞(omv)ワクチン Download PDFInfo
- Publication number
- JP5823446B2 JP5823446B2 JP2013124554A JP2013124554A JP5823446B2 JP 5823446 B2 JP5823446 B2 JP 5823446B2 JP 2013124554 A JP2013124554 A JP 2013124554A JP 2013124554 A JP2013124554 A JP 2013124554A JP 5823446 B2 JP5823446 B2 JP 5823446B2
- Authority
- JP
- Japan
- Prior art keywords
- protein
- sequence
- composition
- protective antigen
- gene
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000012528 membrane Substances 0.000 title claims abstract description 19
- 229960005486 vaccine Drugs 0.000 title claims description 44
- 101710116435 Outer membrane protein Proteins 0.000 title description 2
- 108090000623 proteins and genes Proteins 0.000 claims abstract description 300
- 102000004169 proteins and genes Human genes 0.000 claims abstract description 204
- 239000000203 mixture Substances 0.000 claims abstract description 99
- 230000002163 immunogen Effects 0.000 claims abstract description 59
- 101710194807 Protective antigen Proteins 0.000 claims abstract description 42
- 241000588650 Neisseria meningitidis Species 0.000 claims abstract description 26
- 241000588653 Neisseria Species 0.000 claims abstract description 21
- 229940009976 deoxycholate Drugs 0.000 claims abstract description 7
- KXGVEGMKQFWNSR-LLQZFEROSA-N deoxycholic acid Chemical compound C([C@H]1CC2)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(O)=O)C)[C@@]2(C)[C@@H](O)C1 KXGVEGMKQFWNSR-LLQZFEROSA-N 0.000 claims abstract description 7
- 238000002360 preparation method Methods 0.000 claims description 21
- 125000003275 alpha amino acid group Chemical group 0.000 claims description 19
- 239000003814 drug Substances 0.000 claims description 13
- 238000011282 treatment Methods 0.000 claims description 9
- 206010043376 Tetanus Diseases 0.000 claims description 8
- 206010013023 diphtheria Diseases 0.000 claims description 8
- 208000015181 infectious disease Diseases 0.000 claims description 7
- 208000000474 Poliomyelitis Diseases 0.000 claims description 6
- 241000606768 Haemophilus influenzae Species 0.000 claims description 5
- 201000005702 Pertussis Diseases 0.000 claims description 5
- 229940047650 haemophilus influenzae Drugs 0.000 claims description 5
- 241000700721 Hepatitis B virus Species 0.000 claims description 4
- 230000002265 prevention Effects 0.000 claims description 4
- 241000590002 Helicobacter pylori Species 0.000 claims description 3
- 229940037467 helicobacter pylori Drugs 0.000 claims description 3
- 238000001514 detection method Methods 0.000 claims 1
- 239000012634 fragment Substances 0.000 abstract description 70
- 238000000605 extraction Methods 0.000 abstract description 6
- 244000052769 pathogen Species 0.000 abstract description 3
- 235000018102 proteins Nutrition 0.000 description 196
- 239000013598 vector Substances 0.000 description 100
- 210000004027 cell Anatomy 0.000 description 94
- 230000014509 gene expression Effects 0.000 description 89
- 238000000034 method Methods 0.000 description 50
- 108020004414 DNA Proteins 0.000 description 49
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 47
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 description 44
- 108091007433 antigens Proteins 0.000 description 39
- 102000036639 antigens Human genes 0.000 description 39
- 239000000427 antigen Substances 0.000 description 38
- 241000196324 Embryophyta Species 0.000 description 33
- 108090000765 processed proteins & peptides Proteins 0.000 description 31
- 102000004196 processed proteins & peptides Human genes 0.000 description 30
- 241000700605 Viruses Species 0.000 description 29
- 229920001184 polypeptide Polymers 0.000 description 28
- 241000701447 unidentified baculovirus Species 0.000 description 26
- 239000002502 liposome Substances 0.000 description 25
- 150000007523 nucleic acids Chemical class 0.000 description 25
- 241000588724 Escherichia coli Species 0.000 description 24
- 230000001580 bacterial effect Effects 0.000 description 24
- 239000013612 plasmid Substances 0.000 description 24
- 102000040430 polynucleotide Human genes 0.000 description 24
- 108091033319 polynucleotide Proteins 0.000 description 24
- 239000002157 polynucleotide Substances 0.000 description 24
- 108091026890 Coding region Proteins 0.000 description 23
- 108010076504 Protein Sorting Signals Proteins 0.000 description 23
- 230000001105 regulatory effect Effects 0.000 description 23
- 108091028043 Nucleic acid sequence Proteins 0.000 description 21
- 230000027455 binding Effects 0.000 description 21
- 230000035897 transcription Effects 0.000 description 21
- 238000013518 transcription Methods 0.000 description 21
- 102000039446 nucleic acids Human genes 0.000 description 20
- 108020004707 nucleic acids Proteins 0.000 description 20
- 241000894006 Bacteria Species 0.000 description 19
- 150000004676 glycans Chemical class 0.000 description 19
- 229920001282 polysaccharide Polymers 0.000 description 19
- 239000005017 polysaccharide Substances 0.000 description 19
- 239000003795 chemical substances by application Substances 0.000 description 18
- 108090001030 Lipoproteins Proteins 0.000 description 17
- 102000004895 Lipoproteins Human genes 0.000 description 17
- 238000009396 hybridization Methods 0.000 description 17
- 239000002773 nucleotide Substances 0.000 description 17
- 125000003729 nucleotide group Chemical group 0.000 description 17
- 108090000790 Enzymes Proteins 0.000 description 16
- 235000001014 amino acid Nutrition 0.000 description 16
- 238000001415 gene therapy Methods 0.000 description 16
- 230000010076 replication Effects 0.000 description 16
- 230000009466 transformation Effects 0.000 description 16
- 102000004190 Enzymes Human genes 0.000 description 15
- 241000238631 Hexapoda Species 0.000 description 15
- 229940088598 enzyme Drugs 0.000 description 15
- 150000002632 lipids Chemical class 0.000 description 15
- 238000000338 in vitro Methods 0.000 description 14
- 230000028327 secretion Effects 0.000 description 14
- 238000012546 transfer Methods 0.000 description 14
- 239000003981 vehicle Substances 0.000 description 14
- 239000002671 adjuvant Substances 0.000 description 13
- 230000004927 fusion Effects 0.000 description 13
- 239000000523 sample Substances 0.000 description 13
- 102000004163 DNA-directed RNA polymerases Human genes 0.000 description 12
- 102000037865 fusion proteins Human genes 0.000 description 12
- 108020001507 fusion proteins Proteins 0.000 description 12
- 210000004962 mammalian cell Anatomy 0.000 description 12
- 239000002245 particle Substances 0.000 description 12
- 230000001177 retroviral effect Effects 0.000 description 12
- 150000001413 amino acids Chemical class 0.000 description 11
- 238000003556 assay Methods 0.000 description 11
- 230000000694 effects Effects 0.000 description 11
- 239000013604 expression vector Substances 0.000 description 11
- 230000005030 transcription termination Effects 0.000 description 11
- 108010083590 Apoproteins Proteins 0.000 description 10
- 108090000626 DNA-directed RNA polymerases Proteins 0.000 description 10
- 239000003153 chemical reaction reagent Substances 0.000 description 10
- 239000003623 enhancer Substances 0.000 description 10
- 230000010354 integration Effects 0.000 description 10
- 108020004999 messenger RNA Proteins 0.000 description 10
- 230000003612 virological effect Effects 0.000 description 10
- FWMNVWWHGCHHJJ-SKKKGAJSSA-N 4-amino-1-[(2r)-6-amino-2-[[(2r)-2-[[(2r)-2-[[(2r)-2-amino-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]piperidine-4-carboxylic acid Chemical compound C([C@H](C(=O)N[C@H](CC(C)C)C(=O)N[C@H](CCCCN)C(=O)N1CCC(N)(CC1)C(O)=O)NC(=O)[C@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 FWMNVWWHGCHHJJ-SKKKGAJSSA-N 0.000 description 9
- 102000006410 Apoproteins Human genes 0.000 description 9
- 239000003937 drug carrier Substances 0.000 description 9
- 238000001727 in vivo Methods 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 150000003839 salts Chemical class 0.000 description 9
- 210000001519 tissue Anatomy 0.000 description 9
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 8
- -1 PilC Proteins 0.000 description 8
- 101710182846 Polyhedrin Proteins 0.000 description 8
- 238000013459 approach Methods 0.000 description 8
- 238000010367 cloning Methods 0.000 description 8
- 238000001476 gene delivery Methods 0.000 description 8
- 238000002347 injection Methods 0.000 description 8
- 239000007924 injection Substances 0.000 description 8
- 239000002609 medium Substances 0.000 description 8
- 238000012545 processing Methods 0.000 description 8
- 210000001938 protoplast Anatomy 0.000 description 8
- 241000894007 species Species 0.000 description 8
- 230000005026 transcription initiation Effects 0.000 description 8
- 238000011144 upstream manufacturing Methods 0.000 description 8
- 239000013603 viral vector Substances 0.000 description 8
- 102000053602 DNA Human genes 0.000 description 7
- 108010008281 Recombinant Fusion Proteins Proteins 0.000 description 7
- 102000007056 Recombinant Fusion Proteins Human genes 0.000 description 7
- 108091081024 Start codon Proteins 0.000 description 7
- IXKSXJFAGXLQOQ-XISFHERQSA-N WHWLQLKPGQPMY Chemical compound C([C@@H](C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(O)=O)NC(=O)[C@@H](N)CC=1C2=CC=CC=C2NC=1)C1=CNC=N1 IXKSXJFAGXLQOQ-XISFHERQSA-N 0.000 description 7
- 230000000977 initiatory effect Effects 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 230000001404 mediated effect Effects 0.000 description 7
- 229930182817 methionine Natural products 0.000 description 7
- 229940124597 therapeutic agent Drugs 0.000 description 7
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N (+)-Biotin Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 101000833492 Homo sapiens Jouberin Proteins 0.000 description 6
- 101000651236 Homo sapiens NCK-interacting protein with SH3 domain Proteins 0.000 description 6
- 102100024407 Jouberin Human genes 0.000 description 6
- 108090000848 Ubiquitin Proteins 0.000 description 6
- 102000044159 Ubiquitin Human genes 0.000 description 6
- 230000000844 anti-bacterial effect Effects 0.000 description 6
- 239000000969 carrier Substances 0.000 description 6
- 238000005516 engineering process Methods 0.000 description 6
- 238000009472 formulation Methods 0.000 description 6
- 230000003053 immunization Effects 0.000 description 6
- 238000003018 immunoassay Methods 0.000 description 6
- 238000003780 insertion Methods 0.000 description 6
- 230000037431 insertion Effects 0.000 description 6
- 239000003446 ligand Substances 0.000 description 6
- 239000003550 marker Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 241001515965 unidentified phage Species 0.000 description 6
- 239000013607 AAV vector Substances 0.000 description 5
- 241000710929 Alphavirus Species 0.000 description 5
- 229920002307 Dextran Polymers 0.000 description 5
- 102000014150 Interferons Human genes 0.000 description 5
- 108010050904 Interferons Proteins 0.000 description 5
- 241001465754 Metazoa Species 0.000 description 5
- 206010028980 Neoplasm Diseases 0.000 description 5
- 101150075249 ORF40 gene Proteins 0.000 description 5
- 101100156835 Paenarthrobacter nicotinovorans xdh gene Proteins 0.000 description 5
- 108700009124 Transcription Initiation Site Proteins 0.000 description 5
- 101000626900 Trieres chinensis Uncharacterized 5.5 kDa protein in ccsA-rps6 intergenic region Proteins 0.000 description 5
- 239000011324 bead Substances 0.000 description 5
- 230000001851 biosynthetic effect Effects 0.000 description 5
- 210000004369 blood Anatomy 0.000 description 5
- 239000008280 blood Substances 0.000 description 5
- 238000007796 conventional method Methods 0.000 description 5
- 229960002086 dextran Drugs 0.000 description 5
- 238000004520 electroporation Methods 0.000 description 5
- 230000006870 function Effects 0.000 description 5
- 239000001963 growth medium Substances 0.000 description 5
- 229940088597 hormone Drugs 0.000 description 5
- 239000005556 hormone Substances 0.000 description 5
- 230000002209 hydrophobic effect Effects 0.000 description 5
- 238000002649 immunization Methods 0.000 description 5
- 238000011534 incubation Methods 0.000 description 5
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 5
- 238000010369 molecular cloning Methods 0.000 description 5
- 239000008194 pharmaceutical composition Substances 0.000 description 5
- 230000008488 polyadenylation Effects 0.000 description 5
- OXCMYAYHXIHQOA-UHFFFAOYSA-N potassium;[2-butyl-5-chloro-3-[[4-[2-(1,2,4-triaza-3-azanidacyclopenta-1,4-dien-5-yl)phenyl]phenyl]methyl]imidazol-4-yl]methanol Chemical compound [K+].CCCCC1=NC(Cl)=C(CO)N1CC1=CC=C(C=2C(=CC=CC=2)C2=N[N-]N=N2)C=C1 OXCMYAYHXIHQOA-UHFFFAOYSA-N 0.000 description 5
- 210000002966 serum Anatomy 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 230000001225 therapeutic effect Effects 0.000 description 5
- 238000001890 transfection Methods 0.000 description 5
- 238000013519 translation Methods 0.000 description 5
- 241000701161 unidentified adenovirus Species 0.000 description 5
- 108091032973 (ribonucleotides)n+m Proteins 0.000 description 4
- 108090001008 Avidin Proteins 0.000 description 4
- 241000193830 Bacillus <bacterium> Species 0.000 description 4
- 101000874355 Escherichia coli (strain K12) Outer membrane protein assembly factor BamA Proteins 0.000 description 4
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 4
- 201000009906 Meningitis Diseases 0.000 description 4
- 241000714177 Murine leukemia virus Species 0.000 description 4
- 241000588652 Neisseria gonorrhoeae Species 0.000 description 4
- 102000007327 Protamines Human genes 0.000 description 4
- 108010007568 Protamines Proteins 0.000 description 4
- 108700026226 TATA Box Proteins 0.000 description 4
- 108091023040 Transcription factor Proteins 0.000 description 4
- 108010031133 Transferrin-Binding Protein A Proteins 0.000 description 4
- 108010031127 Transferrin-Binding Protein B Proteins 0.000 description 4
- 230000003321 amplification Effects 0.000 description 4
- 230000033228 biological regulation Effects 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 125000002091 cationic group Chemical group 0.000 description 4
- 150000001768 cations Chemical class 0.000 description 4
- 238000004113 cell culture Methods 0.000 description 4
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 4
- 210000000349 chromosome Anatomy 0.000 description 4
- 238000010276 construction Methods 0.000 description 4
- ATDGTVJJHBUTRL-UHFFFAOYSA-N cyanogen bromide Chemical compound BrC#N ATDGTVJJHBUTRL-UHFFFAOYSA-N 0.000 description 4
- MWRBNPKJOOWZPW-CLFAGFIQSA-N dioleoyl phosphatidylethanolamine Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(COP(O)(=O)OCCN)OC(=O)CCCCCCC\C=C/CCCCCCCC MWRBNPKJOOWZPW-CLFAGFIQSA-N 0.000 description 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 230000028993 immune response Effects 0.000 description 4
- 230000001976 improved effect Effects 0.000 description 4
- 230000001939 inductive effect Effects 0.000 description 4
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 description 4
- 229940079322 interferon Drugs 0.000 description 4
- 238000003199 nucleic acid amplification method Methods 0.000 description 4
- 238000004806 packaging method and process Methods 0.000 description 4
- 230000006798 recombination Effects 0.000 description 4
- 238000005215 recombination Methods 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- 230000005945 translocation Effects 0.000 description 4
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 4
- 241001430294 unidentified retrovirus Species 0.000 description 4
- YYGNTYWPHWGJRM-UHFFFAOYSA-N (6E,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene Chemical compound CC(C)=CCCC(C)=CCCC(C)=CCCC=C(C)CCC=C(C)CCC=C(C)C YYGNTYWPHWGJRM-UHFFFAOYSA-N 0.000 description 3
- KSXTUUUQYQYKCR-LQDDAWAPSA-M 2,3-bis[[(z)-octadec-9-enoyl]oxy]propyl-trimethylazanium;chloride Chemical compound [Cl-].CCCCCCCC\C=C/CCCCCCCC(=O)OCC(C[N+](C)(C)C)OC(=O)CCCCCCC\C=C/CCCCCCCC KSXTUUUQYQYKCR-LQDDAWAPSA-M 0.000 description 3
- 108010088751 Albumins Proteins 0.000 description 3
- 102000009027 Albumins Human genes 0.000 description 3
- 102000007698 Alcohol dehydrogenase Human genes 0.000 description 3
- 108010021809 Alcohol dehydrogenase Proteins 0.000 description 3
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 3
- 108010039939 Cell Wall Skeleton Proteins 0.000 description 3
- 108010004103 Chylomicrons Proteins 0.000 description 3
- 108020004705 Codon Proteins 0.000 description 3
- 102100031725 Cortactin-binding protein 2 Human genes 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- 108091029865 Exogenous DNA Proteins 0.000 description 3
- 229920000209 Hexadimethrine bromide Polymers 0.000 description 3
- 206010020649 Hyperkeratosis Diseases 0.000 description 3
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 3
- 108010046938 Macrophage Colony-Stimulating Factor Proteins 0.000 description 3
- 102000007651 Macrophage Colony-Stimulating Factor Human genes 0.000 description 3
- 241000124008 Mammalia Species 0.000 description 3
- 241000699666 Mus <mouse, genus> Species 0.000 description 3
- 241000699670 Mus sp. Species 0.000 description 3
- 241000040340 Oat mosaic virus Species 0.000 description 3
- 241000283973 Oryctolagus cuniculus Species 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- 108010039918 Polylysine Proteins 0.000 description 3
- 101710197985 Probable protein Rev Proteins 0.000 description 3
- 102000013009 Pyruvate Kinase Human genes 0.000 description 3
- 108020005115 Pyruvate Kinase Proteins 0.000 description 3
- 241000714474 Rous sarcoma virus Species 0.000 description 3
- 241000700584 Simplexvirus Species 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- BHEOSNUKNHRBNM-UHFFFAOYSA-N Tetramethylsqualene Natural products CC(=C)C(C)CCC(=C)C(C)CCC(C)=CCCC=C(C)CCC(C)C(=C)CCC(C)C(C)=C BHEOSNUKNHRBNM-UHFFFAOYSA-N 0.000 description 3
- 102000040945 Transcription factor Human genes 0.000 description 3
- 102000004338 Transferrin Human genes 0.000 description 3
- 108090000901 Transferrin Proteins 0.000 description 3
- 108700005077 Viral Genes Proteins 0.000 description 3
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 3
- 229960000723 ampicillin Drugs 0.000 description 3
- AVKUERGKIZMTKX-NJBDSQKTSA-N ampicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=CC=C1 AVKUERGKIZMTKX-NJBDSQKTSA-N 0.000 description 3
- 230000000890 antigenic effect Effects 0.000 description 3
- 108010084541 asialoorosomucoid Proteins 0.000 description 3
- 229960002685 biotin Drugs 0.000 description 3
- 235000020958 biotin Nutrition 0.000 description 3
- 239000011616 biotin Substances 0.000 description 3
- 239000000872 buffer Substances 0.000 description 3
- 201000011510 cancer Diseases 0.000 description 3
- 210000002421 cell wall Anatomy 0.000 description 3
- 210000004520 cell wall skeleton Anatomy 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000003776 cleavage reaction Methods 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 238000002716 delivery method Methods 0.000 description 3
- 238000013461 design Methods 0.000 description 3
- 201000010099 disease Diseases 0.000 description 3
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N dodecahydrosqualene Natural products CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 210000002257 embryonic structure Anatomy 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000005538 encapsulation Methods 0.000 description 3
- 230000002708 enhancing effect Effects 0.000 description 3
- 229930182830 galactose Natural products 0.000 description 3
- 230000002068 genetic effect Effects 0.000 description 3
- 238000002744 homologous recombination Methods 0.000 description 3
- 230000006801 homologous recombination Effects 0.000 description 3
- 210000004408 hybridoma Anatomy 0.000 description 3
- 230000003308 immunostimulating effect Effects 0.000 description 3
- 239000008101 lactose Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000037353 metabolic pathway Effects 0.000 description 3
- 125000001360 methionine group Chemical group N[C@@H](CCSC)C(=O)* 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000007899 nucleic acid hybridization Methods 0.000 description 3
- 210000004940 nucleus Anatomy 0.000 description 3
- 235000015097 nutrients Nutrition 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 229920000656 polylysine Polymers 0.000 description 3
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 3
- 229920000053 polysorbate 80 Polymers 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 229940048914 protamine Drugs 0.000 description 3
- 230000002685 pulmonary effect Effects 0.000 description 3
- 230000002285 radioactive effect Effects 0.000 description 3
- 230000008929 regeneration Effects 0.000 description 3
- 238000011069 regeneration method Methods 0.000 description 3
- 230000007017 scission Effects 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- 230000009870 specific binding Effects 0.000 description 3
- 229940031439 squalene Drugs 0.000 description 3
- TUHBEKDERLKLEC-UHFFFAOYSA-N squalene Natural products CC(=CCCC(=CCCC(=CCCC=C(/C)CCC=C(/C)CC=C(C)C)C)C)C TUHBEKDERLKLEC-UHFFFAOYSA-N 0.000 description 3
- 238000010561 standard procedure Methods 0.000 description 3
- 239000000829 suppository Substances 0.000 description 3
- 230000008685 targeting Effects 0.000 description 3
- 239000003053 toxin Substances 0.000 description 3
- 231100000765 toxin Toxicity 0.000 description 3
- 108700012359 toxins Proteins 0.000 description 3
- 239000012581 transferrin Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- SNKAWJBJQDLSFF-NVKMUCNASA-N 1,2-dioleoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/CCCCCCCC SNKAWJBJQDLSFF-NVKMUCNASA-N 0.000 description 2
- LDGWQMRUWMSZIU-LQDDAWAPSA-M 2,3-bis[(z)-octadec-9-enoxy]propyl-trimethylazanium;chloride Chemical compound [Cl-].CCCCCCCC\C=C/CCCCCCCCOCC(C[N+](C)(C)C)OCCCCCCCC\C=C/CCCCCCCC LDGWQMRUWMSZIU-LQDDAWAPSA-M 0.000 description 2
- 241000589158 Agrobacterium Species 0.000 description 2
- 108010032595 Antibody Binding Sites Proteins 0.000 description 2
- 108020004513 Bacterial RNA Proteins 0.000 description 2
- 241000283707 Capra Species 0.000 description 2
- 101710132601 Capsid protein Proteins 0.000 description 2
- 108010060123 Conjugate Vaccines Proteins 0.000 description 2
- 241000711573 Coronaviridae Species 0.000 description 2
- 230000004568 DNA-binding Effects 0.000 description 2
- ULGZDMOVFRHVEP-RWJQBGPGSA-N Erythromycin Chemical compound O([C@@H]1[C@@H](C)C(=O)O[C@@H]([C@@]([C@H](O)[C@@H](C)C(=O)[C@H](C)C[C@@](C)(O)[C@H](O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)[C@H]1C)(C)O)CC)[C@H]1C[C@@](C)(OC)[C@@H](O)[C@H](C)O1 ULGZDMOVFRHVEP-RWJQBGPGSA-N 0.000 description 2
- 108010058643 Fungal Proteins Proteins 0.000 description 2
- 102100039556 Galectin-4 Human genes 0.000 description 2
- 108700028146 Genetic Enhancer Elements Proteins 0.000 description 2
- 239000005980 Gibberellic acid Substances 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- 108010017080 Granulocyte Colony-Stimulating Factor Proteins 0.000 description 2
- 102000004269 Granulocyte Colony-Stimulating Factor Human genes 0.000 description 2
- 108010010234 HDL Lipoproteins Proteins 0.000 description 2
- 101000608765 Homo sapiens Galectin-4 Proteins 0.000 description 2
- 240000005979 Hordeum vulgare Species 0.000 description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 description 2
- 108010060231 Insect Proteins Proteins 0.000 description 2
- 102000004877 Insulin Human genes 0.000 description 2
- 108090001061 Insulin Proteins 0.000 description 2
- 102100034349 Integrase Human genes 0.000 description 2
- 108010063738 Interleukins Proteins 0.000 description 2
- 102000015696 Interleukins Human genes 0.000 description 2
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 description 2
- 108010007622 LDL Lipoproteins Proteins 0.000 description 2
- 241000219823 Medicago Species 0.000 description 2
- 241000713862 Moloney murine sarcoma virus Species 0.000 description 2
- 108091061960 Naked DNA Proteins 0.000 description 2
- 241000588656 Neisseriaceae Species 0.000 description 2
- 101150012394 PHO5 gene Proteins 0.000 description 2
- 108091093037 Peptide nucleic acid Proteins 0.000 description 2
- 241000235648 Pichia Species 0.000 description 2
- 108700001094 Plant Genes Proteins 0.000 description 2
- UTPGJEROJZHISI-UHFFFAOYSA-N Pleniradin-acetat Natural products C1=C(C)C2C(OC(=O)C)CC(C)(O)C2CC2C(=C)C(=O)OC21 UTPGJEROJZHISI-UHFFFAOYSA-N 0.000 description 2
- 229920000954 Polyglycolide Polymers 0.000 description 2
- 108010076039 Polyproteins Proteins 0.000 description 2
- 108020005067 RNA Splice Sites Proteins 0.000 description 2
- 230000006819 RNA synthesis Effects 0.000 description 2
- 241000700159 Rattus Species 0.000 description 2
- 108020004511 Recombinant DNA Proteins 0.000 description 2
- 241000710960 Sindbis virus Species 0.000 description 2
- 241000194017 Streptococcus Species 0.000 description 2
- 102000019197 Superoxide Dismutase Human genes 0.000 description 2
- 108010012715 Superoxide dismutase Proteins 0.000 description 2
- 108700005078 Synthetic Genes Proteins 0.000 description 2
- 239000004098 Tetracycline Substances 0.000 description 2
- IQFYYKKMVGJFEH-XLPZGREQSA-N Thymidine Chemical compound O=C1NC(=O)C(C)=CN1[C@@H]1O[C@H](CO)[C@@H](O)C1 IQFYYKKMVGJFEH-XLPZGREQSA-N 0.000 description 2
- 102100023132 Transcription factor Jun Human genes 0.000 description 2
- QIVBCDIJIAJPQS-UHFFFAOYSA-N Tryptophan Natural products C1=CC=C2C(CC(N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-UHFFFAOYSA-N 0.000 description 2
- 108060008682 Tumor Necrosis Factor Proteins 0.000 description 2
- 108010062497 VLDL Lipoproteins Proteins 0.000 description 2
- 208000036142 Viral infection Diseases 0.000 description 2
- DSNRWDQKZIEDDB-GCMPNPAFSA-N [(2r)-3-[2,3-dihydroxypropoxy(hydroxy)phosphoryl]oxy-2-[(z)-octadec-9-enoyl]oxypropyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@H](COP(O)(=O)OCC(O)CO)OC(=O)CCCCCCC\C=C/CCCCCCCC DSNRWDQKZIEDDB-GCMPNPAFSA-N 0.000 description 2
- HMNZFMSWFCAGGW-XPWSMXQVSA-N [3-[hydroxy(2-hydroxyethoxy)phosphoryl]oxy-2-[(e)-octadec-9-enoyl]oxypropyl] (e)-octadec-9-enoate Chemical compound CCCCCCCC\C=C\CCCCCCCC(=O)OCC(COP(O)(=O)OCCO)OC(=O)CCCCCCC\C=C\CCCCCCCC HMNZFMSWFCAGGW-XPWSMXQVSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- 108091006088 activator proteins Proteins 0.000 description 2
- 238000001042 affinity chromatography Methods 0.000 description 2
- NWMHDZMRVUOQGL-CZEIJOLGSA-N almurtide Chemical compound OC(=O)CC[C@H](C(N)=O)NC(=O)[C@H](C)NC(=O)CO[C@@H]([C@H](O)[C@H](O)CO)[C@@H](NC(C)=O)C=O NWMHDZMRVUOQGL-CZEIJOLGSA-N 0.000 description 2
- 229940037003 alum Drugs 0.000 description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 2
- 125000000539 amino acid group Chemical group 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 210000003719 b-lymphocyte Anatomy 0.000 description 2
- 210000003578 bacterial chromosome Anatomy 0.000 description 2
- 229910000389 calcium phosphate Inorganic materials 0.000 description 2
- 239000001506 calcium phosphate Substances 0.000 description 2
- 235000011010 calcium phosphates Nutrition 0.000 description 2
- 235000012000 cholesterol Nutrition 0.000 description 2
- 229940031670 conjugate vaccine Drugs 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 229960000633 dextran sulfate Drugs 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 201000002491 encephalomyelitis Diseases 0.000 description 2
- OVBPIULPVIDEAO-LBPRGKRZSA-N folic acid Chemical compound C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-LBPRGKRZSA-N 0.000 description 2
- 238000010353 genetic engineering Methods 0.000 description 2
- IXORZMNAPKEEDV-UHFFFAOYSA-N gibberellic acid GA3 Natural products OC(=O)C1C2(C3)CC(=C)C3(O)CCC2C2(C=CC3O)C1C3(C)C(=O)O2 IXORZMNAPKEEDV-UHFFFAOYSA-N 0.000 description 2
- IXORZMNAPKEEDV-OBDJNFEBSA-N gibberellin A3 Chemical compound C([C@@]1(O)C(=C)C[C@@]2(C1)[C@H]1C(O)=O)C[C@H]2[C@]2(C=C[C@@H]3O)[C@H]1[C@]3(C)C(=O)O2 IXORZMNAPKEEDV-OBDJNFEBSA-N 0.000 description 2
- 108020004445 glyceraldehyde-3-phosphate dehydrogenase Proteins 0.000 description 2
- 230000002414 glycolytic effect Effects 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 239000000017 hydrogel Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- FDGQSTZJBFJUBT-UHFFFAOYSA-N hypoxanthine Chemical compound O=C1NC=NC2=C1NC=N2 FDGQSTZJBFJUBT-UHFFFAOYSA-N 0.000 description 2
- 230000036039 immunity Effects 0.000 description 2
- 230000005847 immunogenicity Effects 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229940125396 insulin Drugs 0.000 description 2
- 230000003834 intracellular effect Effects 0.000 description 2
- 230000005865 ionizing radiation Effects 0.000 description 2
- 210000003734 kidney Anatomy 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 230000003902 lesion Effects 0.000 description 2
- 239000006193 liquid solution Substances 0.000 description 2
- 239000006194 liquid suspension Substances 0.000 description 2
- 229920002521 macromolecule Polymers 0.000 description 2
- 210000002540 macrophage Anatomy 0.000 description 2
- 238000000520 microinjection Methods 0.000 description 2
- 239000011859 microparticle Substances 0.000 description 2
- JMUHBNWAORSSBD-WKYWBUFDSA-N mifamurtide Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCCCCCCCCCC)COP(O)(=O)OCCNC(=O)[C@H](C)NC(=O)CC[C@H](C(N)=O)NC(=O)[C@H](C)NC(=O)[C@@H](C)O[C@H]1[C@H](O)[C@@H](CO)OC(O)[C@@H]1NC(C)=O JMUHBNWAORSSBD-WKYWBUFDSA-N 0.000 description 2
- 229960005225 mifamurtide Drugs 0.000 description 2
- 125000001446 muramyl group Chemical group N[C@@H](C=O)[C@@H](O[C@@H](C(=O)*)C)[C@H](O)[C@H](O)CO 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 239000006179 pH buffering agent Substances 0.000 description 2
- 230000007170 pathology Effects 0.000 description 2
- 229920000747 poly(lactic acid) Polymers 0.000 description 2
- 229920001515 polyalkylene glycol Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229940031937 polysaccharide vaccine Drugs 0.000 description 2
- 230000029279 positive regulation of transcription, DNA-dependent Effects 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 230000000069 prophylactic effect Effects 0.000 description 2
- 238000001742 protein purification Methods 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 2
- 238000003259 recombinant expression Methods 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 108091008146 restriction endonucleases Proteins 0.000 description 2
- 238000012552 review Methods 0.000 description 2
- 239000013605 shuttle vector Substances 0.000 description 2
- 238000002415 sodium dodecyl sulfate polyacrylamide gel electrophoresis Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- ATHGHQPFGPMSJY-UHFFFAOYSA-N spermidine Chemical compound NCCCCNCCCN ATHGHQPFGPMSJY-UHFFFAOYSA-N 0.000 description 2
- PFNFFQXMRSDOHW-UHFFFAOYSA-N spermine Chemical compound NCCCNCCCCNCCCN PFNFFQXMRSDOHW-UHFFFAOYSA-N 0.000 description 2
- 210000004989 spleen cell Anatomy 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 210000000130 stem cell Anatomy 0.000 description 2
- 229960002180 tetracycline Drugs 0.000 description 2
- 229930101283 tetracycline Natural products 0.000 description 2
- 235000019364 tetracycline Nutrition 0.000 description 2
- 150000003522 tetracyclines Chemical class 0.000 description 2
- XETCRXVKJHBPMK-MJSODCSWSA-N trehalose 6,6'-dimycolate Chemical compound C([C@@H]1[C@H]([C@H](O)[C@@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](COC(=O)C(CCCCCCCCCCC3C(C3)CCCCCCCCCCCCCCCCCC)C(O)CCCCCCCCCCCCCCCCCCCCCCCCC)O2)O)O1)O)OC(=O)C(C(O)CCCCCCCCCCCCCCCCCCCCCCCCC)CCCCCCCCCCC1CC1CCCCCCCCCCCCCCCCCC XETCRXVKJHBPMK-MJSODCSWSA-N 0.000 description 2
- 150000003626 triacylglycerols Chemical class 0.000 description 2
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 2
- 102000003390 tumor necrosis factor Human genes 0.000 description 2
- 108010016264 ubiquitin-Nalpha-protein hydrolase Proteins 0.000 description 2
- 241000712461 unidentified influenza virus Species 0.000 description 2
- 238000002255 vaccination Methods 0.000 description 2
- 230000009385 viral infection Effects 0.000 description 2
- 239000011782 vitamin Substances 0.000 description 2
- 235000013343 vitamin Nutrition 0.000 description 2
- 229940088594 vitamin Drugs 0.000 description 2
- 229930003231 vitamin Natural products 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- 210000005253 yeast cell Anatomy 0.000 description 2
- DRHZYJAUECRAJM-DWSYSWFDSA-N (2s,3s,4s,5r,6r)-6-[[(3s,4s,4ar,6ar,6bs,8r,8ar,12as,14ar,14br)-8a-[(2s,3r,4s,5r,6r)-3-[(2s,3r,4s,5r,6s)-5-[(2s,3r,4s,5r)-4-[(2s,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-5-[(3s,5s, Chemical compound O([C@H]1[C@H](O)[C@H](O[C@H]([C@@H]1O[C@H]1[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O1)O)O[C@H]1CC[C@]2(C)[C@H]3CC=C4[C@@H]5CC(C)(C)CC[C@@]5([C@@H](C[C@@]4(C)[C@]3(C)CC[C@H]2[C@@]1(C=O)C)O)C(=O)O[C@@H]1O[C@H](C)[C@@H]([C@@H]([C@H]1O[C@H]1[C@@H]([C@H](O)[C@@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@](O)(CO)CO3)O)[C@H](O)CO2)O)[C@H](C)O1)O)O)OC(=O)C[C@@H](O)C[C@H](OC(=O)C[C@@H](O)C[C@@H]([C@@H](C)CC)O[C@H]1[C@@H]([C@@H](O)[C@H](CO)O1)O)[C@@H](C)CC)C(O)=O)[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O DRHZYJAUECRAJM-DWSYSWFDSA-N 0.000 description 1
- YHQZWWDVLJPRIF-JLHRHDQISA-N (4R)-4-[[(2S,3R)-2-[acetyl-[(3R,4R,5S,6R)-3-amino-4-[(1R)-1-carboxyethoxy]-5-hydroxy-6-(hydroxymethyl)oxan-2-yl]amino]-3-hydroxybutanoyl]amino]-5-amino-5-oxopentanoic acid Chemical compound C(C)(=O)N([C@@H]([C@H](O)C)C(=O)N[C@H](CCC(=O)O)C(N)=O)C1[C@H](N)[C@@H](O[C@@H](C(=O)O)C)[C@H](O)[C@H](O1)CO YHQZWWDVLJPRIF-JLHRHDQISA-N 0.000 description 1
- GZCWLCBFPRFLKL-UHFFFAOYSA-N 1-prop-2-ynoxypropan-2-ol Chemical compound CC(O)COCC#C GZCWLCBFPRFLKL-UHFFFAOYSA-N 0.000 description 1
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
- PXFBZOLANLWPMH-UHFFFAOYSA-N 16-Epiaffinine Natural products C1C(C2=CC=CC=C2N2)=C2C(=O)CC2C(=CC)CN(C)C1C2CO PXFBZOLANLWPMH-UHFFFAOYSA-N 0.000 description 1
- 108020004465 16S ribosomal RNA Proteins 0.000 description 1
- RYOFERRMXDATKG-YEUCEMRASA-N 2,3-bis[(z)-octadec-9-enoxy]propyl-trimethylazanium Chemical compound CCCCCCCC\C=C/CCCCCCCCOCC(C[N+](C)(C)C)OCCCCCCCC\C=C/CCCCCCCC RYOFERRMXDATKG-YEUCEMRASA-N 0.000 description 1
- UAIUNKRWKOVEES-UHFFFAOYSA-N 3,3',5,5'-tetramethylbenzidine Chemical compound CC1=C(N)C(C)=CC(C=2C=C(C)C(N)=C(C)C=2)=C1 UAIUNKRWKOVEES-UHFFFAOYSA-N 0.000 description 1
- OSJPPGNTCRNQQC-UWTATZPHSA-N 3-phospho-D-glyceric acid Chemical compound OC(=O)[C@H](O)COP(O)(O)=O OSJPPGNTCRNQQC-UWTATZPHSA-N 0.000 description 1
- TVZGACDUOSZQKY-LBPRGKRZSA-N 4-aminofolic acid Chemical compound C1=NC2=NC(N)=NC(N)=C2N=C1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 TVZGACDUOSZQKY-LBPRGKRZSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 102000013563 Acid Phosphatase Human genes 0.000 description 1
- 108010051457 Acid Phosphatase Proteins 0.000 description 1
- 101100295756 Acinetobacter baumannii (strain ATCC 19606 / DSM 30007 / JCM 6841 / CCUG 19606 / CIP 70.34 / NBRC 109757 / NCIMB 12457 / NCTC 12156 / 81) omp38 gene Proteins 0.000 description 1
- 244000179819 Aechmea magdalenae Species 0.000 description 1
- 235000001291 Aechmea magdalenae Nutrition 0.000 description 1
- 241000256118 Aedes aegypti Species 0.000 description 1
- 102000002260 Alkaline Phosphatase Human genes 0.000 description 1
- 108020004774 Alkaline Phosphatase Proteins 0.000 description 1
- 102100034044 All-trans-retinol dehydrogenase [NAD(+)] ADH1B Human genes 0.000 description 1
- 101710193111 All-trans-retinol dehydrogenase [NAD(+)] ADH4 Proteins 0.000 description 1
- 206010003445 Ascites Diseases 0.000 description 1
- 108010002913 Asialoglycoproteins Proteins 0.000 description 1
- 241001106067 Atropa Species 0.000 description 1
- 241000178568 Aura virus Species 0.000 description 1
- 241001203868 Autographa californica Species 0.000 description 1
- 229930192334 Auxin Natural products 0.000 description 1
- 241000271566 Aves Species 0.000 description 1
- 241000714230 Avian leukemia virus Species 0.000 description 1
- 102000019260 B-Cell Antigen Receptors Human genes 0.000 description 1
- 108010012919 B-Cell Antigen Receptors Proteins 0.000 description 1
- 241000304886 Bacilli Species 0.000 description 1
- 244000063299 Bacillus subtilis Species 0.000 description 1
- 235000014469 Bacillus subtilis Nutrition 0.000 description 1
- 108010077805 Bacterial Proteins Proteins 0.000 description 1
- 241001235572 Balantioides coli Species 0.000 description 1
- 241000608319 Bebaru virus Species 0.000 description 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
- DWRXFEITVBNRMK-UHFFFAOYSA-N Beta-D-1-Arabinofuranosylthymine Natural products O=C1NC(=O)C(C)=CN1C1C(O)C(O)C(CO)O1 DWRXFEITVBNRMK-UHFFFAOYSA-N 0.000 description 1
- 241000255789 Bombyx mori Species 0.000 description 1
- 241000588807 Bordetella Species 0.000 description 1
- 241000714266 Bovine leukemia virus Species 0.000 description 1
- 241000701822 Bovine papillomavirus Species 0.000 description 1
- 102100034808 CCAAT/enhancer-binding protein alpha Human genes 0.000 description 1
- 108010071134 CRM197 (non-toxic variant of diphtheria toxin) Proteins 0.000 description 1
- 241000868138 Cabassou virus Species 0.000 description 1
- 101100327917 Caenorhabditis elegans chup-1 gene Proteins 0.000 description 1
- 101100408682 Caenorhabditis elegans pmt-2 gene Proteins 0.000 description 1
- 241000589876 Campylobacter Species 0.000 description 1
- 241000222120 Candida <Saccharomycetales> Species 0.000 description 1
- 241000222122 Candida albicans Species 0.000 description 1
- 241000222128 Candida maltosa Species 0.000 description 1
- 235000002566 Capsicum Nutrition 0.000 description 1
- 240000008574 Capsicum frutescens Species 0.000 description 1
- 102000014914 Carrier Proteins Human genes 0.000 description 1
- 108010078791 Carrier Proteins Proteins 0.000 description 1
- 241000282693 Cercopithecidae Species 0.000 description 1
- 241001502567 Chikungunya virus Species 0.000 description 1
- 241001227713 Chiron Species 0.000 description 1
- 229920001661 Chitosan Polymers 0.000 description 1
- 206010008631 Cholera Diseases 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- 101710094648 Coat protein Proteins 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 241000699800 Cricetinae Species 0.000 description 1
- 241000699802 Cricetulus griseus Species 0.000 description 1
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
- 244000024469 Cucumis prophetarum Species 0.000 description 1
- 235000010071 Cucumis prophetarum Nutrition 0.000 description 1
- 102000004127 Cytokines Human genes 0.000 description 1
- 108090000695 Cytokines Proteins 0.000 description 1
- 108010041986 DNA Vaccines Proteins 0.000 description 1
- 229940021995 DNA vaccine Drugs 0.000 description 1
- 241000450599 DNA viruses Species 0.000 description 1
- 102000052510 DNA-Binding Proteins Human genes 0.000 description 1
- 108700020911 DNA-Binding Proteins Proteins 0.000 description 1
- 241000208296 Datura Species 0.000 description 1
- 241000208175 Daucus Species 0.000 description 1
- 240000001879 Digitalis lutea Species 0.000 description 1
- 108090000204 Dipeptidase 1 Proteins 0.000 description 1
- 241000255601 Drosophila melanogaster Species 0.000 description 1
- 241000991587 Enterovirus C Species 0.000 description 1
- 101710091045 Envelope protein Proteins 0.000 description 1
- 206010066919 Epidemic polyarthritis Diseases 0.000 description 1
- 102000003951 Erythropoietin Human genes 0.000 description 1
- 108090000394 Erythropoietin Proteins 0.000 description 1
- 101000686777 Escherichia phage T7 T7 RNA polymerase Proteins 0.000 description 1
- 241000701959 Escherichia virus Lambda Species 0.000 description 1
- 241000206602 Eukaryota Species 0.000 description 1
- 108010074860 Factor Xa Proteins 0.000 description 1
- 108050000784 Ferritin Proteins 0.000 description 1
- 102000008857 Ferritin Human genes 0.000 description 1
- 238000008416 Ferritin Methods 0.000 description 1
- 241000192125 Firmicutes Species 0.000 description 1
- 241000231322 Fort Morgan virus Species 0.000 description 1
- 241000220223 Fragaria Species 0.000 description 1
- 101150038242 GAL10 gene Proteins 0.000 description 1
- 102100024637 Galectin-10 Human genes 0.000 description 1
- 108700039691 Genetic Promoter Regions Proteins 0.000 description 1
- 241000208152 Geranium Species 0.000 description 1
- 102000030595 Glucokinase Human genes 0.000 description 1
- 108010021582 Glucokinase Proteins 0.000 description 1
- 108010070600 Glucose-6-phosphate isomerase Proteins 0.000 description 1
- 102100031132 Glucose-6-phosphate isomerase Human genes 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- 102100031181 Glyceraldehyde-3-phosphate dehydrogenase Human genes 0.000 description 1
- JZNWSCPGTDBMEW-UHFFFAOYSA-N Glycerophosphorylethanolamin Natural products NCCOP(O)(=O)OCC(O)CO JZNWSCPGTDBMEW-UHFFFAOYSA-N 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 102100021181 Golgi phosphoprotein 3 Human genes 0.000 description 1
- 241000219146 Gossypium Species 0.000 description 1
- 108010017213 Granulocyte-Macrophage Colony-Stimulating Factor Proteins 0.000 description 1
- 102100039620 Granulocyte-macrophage colony-stimulating factor Human genes 0.000 description 1
- 101150069554 HIS4 gene Proteins 0.000 description 1
- 101150029115 HOPX gene Proteins 0.000 description 1
- 241000208818 Helianthus Species 0.000 description 1
- 241000589989 Helicobacter Species 0.000 description 1
- 241000175212 Herpesvirales Species 0.000 description 1
- 102000005548 Hexokinase Human genes 0.000 description 1
- 108700040460 Hexokinases Proteins 0.000 description 1
- 102000006947 Histones Human genes 0.000 description 1
- 108010033040 Histones Proteins 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 101000945515 Homo sapiens CCAAT/enhancer-binding protein alpha Proteins 0.000 description 1
- 101001071515 Homo sapiens Gastrin-releasing peptide Proteins 0.000 description 1
- 101001002657 Homo sapiens Interleukin-2 Proteins 0.000 description 1
- 101001050288 Homo sapiens Transcription factor Jun Proteins 0.000 description 1
- 101001033034 Homo sapiens UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase Proteins 0.000 description 1
- 108010001336 Horseradish Peroxidase Proteins 0.000 description 1
- 102000008100 Human Serum Albumin Human genes 0.000 description 1
- 108091006905 Human Serum Albumin Proteins 0.000 description 1
- 241000701024 Human betaherpesvirus 5 Species 0.000 description 1
- 241000701044 Human gammaherpesvirus 4 Species 0.000 description 1
- 241000725303 Human immunodeficiency virus Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
- 241000208278 Hyoscyamus Species 0.000 description 1
- UGQMRVRMYYASKQ-UHFFFAOYSA-N Hypoxanthine nucleoside Natural products OC1C(O)C(CO)OC1N1C(NC=NC2=O)=C2N=C1 UGQMRVRMYYASKQ-UHFFFAOYSA-N 0.000 description 1
- 108010046315 IDL Lipoproteins Proteins 0.000 description 1
- 108010021625 Immunoglobulin Fragments Proteins 0.000 description 1
- 102000008394 Immunoglobulin Fragments Human genes 0.000 description 1
- 108010061833 Integrases Proteins 0.000 description 1
- 102000006992 Interferon-alpha Human genes 0.000 description 1
- 108010047761 Interferon-alpha Proteins 0.000 description 1
- 102000008070 Interferon-gamma Human genes 0.000 description 1
- 108010074328 Interferon-gamma Proteins 0.000 description 1
- 108010002352 Interleukin-1 Proteins 0.000 description 1
- 108010065805 Interleukin-12 Proteins 0.000 description 1
- 108010002350 Interleukin-2 Proteins 0.000 description 1
- 108090000978 Interleukin-4 Proteins 0.000 description 1
- 108010002616 Interleukin-5 Proteins 0.000 description 1
- 108090001005 Interleukin-6 Proteins 0.000 description 1
- 108010002586 Interleukin-7 Proteins 0.000 description 1
- 108091092195 Intron Proteins 0.000 description 1
- 241000274177 Juniperus sabina Species 0.000 description 1
- 241000235649 Kluyveromyces Species 0.000 description 1
- 244000285963 Kluyveromyces fragilis Species 0.000 description 1
- 235000014663 Kluyveromyces fragilis Nutrition 0.000 description 1
- 241001138401 Kluyveromyces lactis Species 0.000 description 1
- 241000231318 Kyzylagach virus Species 0.000 description 1
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 description 1
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 description 1
- 108010054278 Lac Repressors Proteins 0.000 description 1
- 241000186660 Lactobacillus Species 0.000 description 1
- 241000194034 Lactococcus lactis subsp. cremoris Species 0.000 description 1
- 241000208822 Lactuca Species 0.000 description 1
- 108091026898 Leader sequence (mRNA) Proteins 0.000 description 1
- 241000713666 Lentivirus Species 0.000 description 1
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 description 1
- 241000208204 Linum Species 0.000 description 1
- 102000011965 Lipoprotein Receptors Human genes 0.000 description 1
- 108010061306 Lipoprotein Receptors Proteins 0.000 description 1
- 241000209082 Lolium Species 0.000 description 1
- 101710125418 Major capsid protein Proteins 0.000 description 1
- 241000121629 Majorana Species 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-L Malonate Chemical compound [O-]C(=O)CC([O-])=O OFOBLEOULBTSOW-UHFFFAOYSA-L 0.000 description 1
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
- 240000003183 Manihot esculenta Species 0.000 description 1
- 108091027974 Mature messenger RNA Proteins 0.000 description 1
- 241000608292 Mayaro virus Species 0.000 description 1
- 241000712079 Measles morbillivirus Species 0.000 description 1
- 235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 1
- 206010027202 Meningitis bacterial Diseases 0.000 description 1
- 108090000157 Metallothionein Proteins 0.000 description 1
- 241000714178 Mink cell focus-forming virus Species 0.000 description 1
- 241000713869 Moloney murine leukemia virus Species 0.000 description 1
- 241000713333 Mouse mammary tumor virus Species 0.000 description 1
- 241000868135 Mucambo virus Species 0.000 description 1
- 101001033276 Mus musculus Interleukin-3 Proteins 0.000 description 1
- 101100476480 Mus musculus S100a8 gene Proteins 0.000 description 1
- OVBPIULPVIDEAO-UHFFFAOYSA-N N-Pteroyl-L-glutaminsaeure Natural products C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-UHFFFAOYSA-N 0.000 description 1
- 125000003047 N-acetyl group Chemical group 0.000 description 1
- SQVRNKJHWKZAKO-PFQGKNLYSA-N N-acetyl-beta-neuraminic acid Chemical compound CC(=O)N[C@@H]1[C@@H](O)C[C@@](O)(C(O)=O)O[C@H]1[C@H](O)[C@H](O)CO SQVRNKJHWKZAKO-PFQGKNLYSA-N 0.000 description 1
- 108700015872 N-acetyl-nor-muramyl-L-alanyl-D-isoglutamine Proteins 0.000 description 1
- 241000608287 Ndumu virus Species 0.000 description 1
- 241000588654 Neisseria cinerea Species 0.000 description 1
- 241000588649 Neisseria lactamica Species 0.000 description 1
- 101100459189 Neisseria meningitidis serogroup B (strain MC58) mutS gene Proteins 0.000 description 1
- 240000002853 Nelumbo nucifera Species 0.000 description 1
- 235000006508 Nelumbo nucifera Nutrition 0.000 description 1
- 235000006510 Nelumbo pentapetala Nutrition 0.000 description 1
- 229930193140 Neomycin Natural products 0.000 description 1
- 108700019961 Neoplasm Genes Proteins 0.000 description 1
- 102000048850 Neoplasm Genes Human genes 0.000 description 1
- 241000772415 Neovison vison Species 0.000 description 1
- 241000208125 Nicotiana Species 0.000 description 1
- 102000006570 Non-Histone Chromosomal Proteins Human genes 0.000 description 1
- 108010008964 Non-Histone Chromosomal Proteins Proteins 0.000 description 1
- 108700020497 Nucleopolyhedrovirus polyhedrin Proteins 0.000 description 1
- 101710141454 Nucleoprotein Proteins 0.000 description 1
- 108010036939 Occlusion Body Matrix Proteins Proteins 0.000 description 1
- 241000320412 Ogataea angusta Species 0.000 description 1
- 108091034117 Oligonucleotide Proteins 0.000 description 1
- 241000219830 Onobrychis Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 102100035593 POU domain, class 2, transcription factor 1 Human genes 0.000 description 1
- 101710084414 POU domain, class 2, transcription factor 1 Proteins 0.000 description 1
- 102100035591 POU domain, class 2, transcription factor 2 Human genes 0.000 description 1
- 101710084411 POU domain, class 2, transcription factor 2 Proteins 0.000 description 1
- 241000209117 Panicum Species 0.000 description 1
- 235000006443 Panicum miliaceum subsp. miliaceum Nutrition 0.000 description 1
- 235000009037 Panicum miliaceum subsp. ruderale Nutrition 0.000 description 1
- 241000208181 Pelargonium Species 0.000 description 1
- 241000209046 Pennisetum Species 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- 102000035195 Peptidases Human genes 0.000 description 1
- 102000007079 Peptide Fragments Human genes 0.000 description 1
- 108010081690 Pertussis Toxin Proteins 0.000 description 1
- 240000007377 Petunia x hybrida Species 0.000 description 1
- 102000001105 Phosphofructokinases Human genes 0.000 description 1
- 108010069341 Phosphofructokinases Proteins 0.000 description 1
- 102000012288 Phosphopyruvate Hydratase Human genes 0.000 description 1
- 108010022181 Phosphopyruvate Hydratase Proteins 0.000 description 1
- 235000014676 Phragmites communis Nutrition 0.000 description 1
- 241000709664 Picornaviridae Species 0.000 description 1
- 241000868134 Pixuna virus Species 0.000 description 1
- 108010064851 Plant Proteins Proteins 0.000 description 1
- 206010035226 Plasma cell myeloma Diseases 0.000 description 1
- 101900205473 Plasmodium falciparum Circumsporozoite protein Proteins 0.000 description 1
- 241000276498 Pollachius virens Species 0.000 description 1
- 241001505332 Polyomavirus sp. Species 0.000 description 1
- 241000288906 Primates Species 0.000 description 1
- 101710083689 Probable capsid protein Proteins 0.000 description 1
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Natural products OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 101710188315 Protein X Proteins 0.000 description 1
- 102100027584 Protein c-Fos Human genes 0.000 description 1
- 108010071563 Proto-Oncogene Proteins c-fos Proteins 0.000 description 1
- 241000125945 Protoparvovirus Species 0.000 description 1
- 241000589516 Pseudomonas Species 0.000 description 1
- 101100084022 Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) lapA gene Proteins 0.000 description 1
- 101100408135 Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) phnA gene Proteins 0.000 description 1
- 239000005700 Putrescine Substances 0.000 description 1
- 108010009460 RNA Polymerase II Proteins 0.000 description 1
- 102000009572 RNA Polymerase II Human genes 0.000 description 1
- 241000218206 Ranunculus Species 0.000 description 1
- 108700005075 Regulator Genes Proteins 0.000 description 1
- 108020005091 Replication Origin Proteins 0.000 description 1
- 108010034634 Repressor Proteins Proteins 0.000 description 1
- 241000712909 Reticuloendotheliosis virus Species 0.000 description 1
- 241000710942 Ross River virus Species 0.000 description 1
- 241000235070 Saccharomyces Species 0.000 description 1
- 240000000111 Saccharum officinarum Species 0.000 description 1
- 235000007201 Saccharum officinarum Nutrition 0.000 description 1
- 241000607142 Salmonella Species 0.000 description 1
- 101000650578 Salmonella phage P22 Regulatory protein C3 Proteins 0.000 description 1
- 241001106018 Salpiglossis Species 0.000 description 1
- 206010039491 Sarcoma Diseases 0.000 description 1
- 241000710961 Semliki Forest virus Species 0.000 description 1
- 241000780602 Senecio Species 0.000 description 1
- 206010040047 Sepsis Diseases 0.000 description 1
- 241000287219 Serinus canaria Species 0.000 description 1
- 241000607768 Shigella Species 0.000 description 1
- 241000220261 Sinapis Species 0.000 description 1
- 108010003723 Single-Domain Antibodies Proteins 0.000 description 1
- 241000207763 Solanum Species 0.000 description 1
- 235000002634 Solanum Nutrition 0.000 description 1
- PRXRUNOAOLTIEF-ADSICKODSA-N Sorbitan trioleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCC\C=C/CCCCCCCC PRXRUNOAOLTIEF-ADSICKODSA-N 0.000 description 1
- 240000006394 Sorghum bicolor Species 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
- 238000002105 Southern blotting Methods 0.000 description 1
- 241000713675 Spumavirus Species 0.000 description 1
- 241000191940 Staphylococcus Species 0.000 description 1
- 108010090804 Streptavidin Proteins 0.000 description 1
- 235000014962 Streptococcus cremoris Nutrition 0.000 description 1
- 244000057717 Streptococcus lactis Species 0.000 description 1
- 235000014897 Streptococcus lactis Nutrition 0.000 description 1
- 241000187398 Streptomyces lividans Species 0.000 description 1
- 235000021536 Sugar beet Nutrition 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 102100040296 TATA-box-binding protein Human genes 0.000 description 1
- 108091036066 Three prime untranslated region Proteins 0.000 description 1
- 102000006601 Thymidine Kinase Human genes 0.000 description 1
- 108020004440 Thymidine kinase Proteins 0.000 description 1
- 241000868137 Tonate virus Species 0.000 description 1
- 108010018242 Transcription Factor AP-1 Proteins 0.000 description 1
- 108010083268 Transcription Factor TFIID Proteins 0.000 description 1
- 102100022972 Transcription factor AP-2-alpha Human genes 0.000 description 1
- 101710189834 Transcription factor AP-2-alpha Proteins 0.000 description 1
- 108020004566 Transfer RNA Proteins 0.000 description 1
- 241000219793 Trifolium Species 0.000 description 1
- 241001312519 Trigonella Species 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 101001040920 Triticum aestivum Alpha-amylase inhibitor 0.28 Proteins 0.000 description 1
- YJQCOFNZVFGCAF-UHFFFAOYSA-N Tunicamycin II Natural products O1C(CC(O)C2C(C(O)C(O2)N2C(NC(=O)C=C2)=O)O)C(O)C(O)C(NC(=O)C=CCCCCCCCCC(C)C)C1OC1OC(CO)C(O)C(O)C1NC(C)=O YJQCOFNZVFGCAF-UHFFFAOYSA-N 0.000 description 1
- 102100038413 UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase Human genes 0.000 description 1
- 241000608278 Una virus Species 0.000 description 1
- 108010046334 Urease Proteins 0.000 description 1
- 241000700618 Vaccinia virus Species 0.000 description 1
- 241000710959 Venezuelan equine encephalitis virus Species 0.000 description 1
- 241000251539 Vertebrata <Metazoa> Species 0.000 description 1
- 241000219977 Vigna Species 0.000 description 1
- 241000235015 Yarrowia lipolytica Species 0.000 description 1
- 241000607734 Yersinia <bacteria> Species 0.000 description 1
- 241000209149 Zea Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- JLCPHMBAVCMARE-UHFFFAOYSA-N [3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methyl [5-(6-aminopurin-9-yl)-2-(hydroxymethyl)oxolan-3-yl] hydrogen phosphate Polymers Cc1cn(C2CC(OP(O)(=O)OCC3OC(CC3OP(O)(=O)OCC3OC(CC3O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c3nc(N)[nH]c4=O)C(COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3CO)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cc(C)c(=O)[nH]c3=O)n3cc(C)c(=O)[nH]c3=O)n3ccc(N)nc3=O)n3cc(C)c(=O)[nH]c3=O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)O2)c(=O)[nH]c1=O JLCPHMBAVCMARE-UHFFFAOYSA-N 0.000 description 1
- 108010022164 acetyl-LDL Proteins 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 230000000240 adjuvant effect Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 108010050181 aleurone Proteins 0.000 description 1
- 108090000637 alpha-Amylases Proteins 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 229960003896 aminopterin Drugs 0.000 description 1
- 239000003098 androgen Substances 0.000 description 1
- 229940030486 androgens Drugs 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 230000001745 anti-biotin effect Effects 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 101150042295 arfA gene Proteins 0.000 description 1
- 238000003491 array Methods 0.000 description 1
- 244000309743 astrovirus Species 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000003416 augmentation Effects 0.000 description 1
- 230000005784 autoimmunity Effects 0.000 description 1
- 238000000376 autoradiography Methods 0.000 description 1
- 239000002363 auxin Substances 0.000 description 1
- 201000009904 bacterial meningitis Diseases 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 108010051210 beta-Fructofuranosidase Proteins 0.000 description 1
- IQFYYKKMVGJFEH-UHFFFAOYSA-N beta-L-thymidine Natural products O=C1NC(=O)C(C)=CN1C1OC(CO)C(O)C1 IQFYYKKMVGJFEH-UHFFFAOYSA-N 0.000 description 1
- SQVRNKJHWKZAKO-UHFFFAOYSA-N beta-N-Acetyl-D-neuraminic acid Natural products CC(=O)NC1C(O)CC(O)(C(O)=O)OC1C(O)C(O)CO SQVRNKJHWKZAKO-UHFFFAOYSA-N 0.000 description 1
- 102000006635 beta-lactamase Human genes 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 239000012472 biological sample Substances 0.000 description 1
- 230000006696 biosynthetic metabolic pathway Effects 0.000 description 1
- 239000001055 blue pigment Substances 0.000 description 1
- 230000036760 body temperature Effects 0.000 description 1
- 229940095731 candida albicans Drugs 0.000 description 1
- 239000001390 capsicum minimum Substances 0.000 description 1
- 239000006143 cell culture medium Substances 0.000 description 1
- 238000012832 cell culture technique Methods 0.000 description 1
- 239000006285 cell suspension Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 230000005591 charge neutralization Effects 0.000 description 1
- 229960005091 chloramphenicol Drugs 0.000 description 1
- WIIZWVCIJKGZOK-RKDXNWHRSA-N chloramphenicol Chemical compound ClC(Cl)C(=O)N[C@H](CO)[C@H](O)C1=CC=C([N+]([O-])=O)C=C1 WIIZWVCIJKGZOK-RKDXNWHRSA-N 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 230000002759 chromosomal effect Effects 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 229940001442 combination vaccine Drugs 0.000 description 1
- 238000012875 competitive assay Methods 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 239000002299 complementary DNA Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 229910001431 copper ion Inorganic materials 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 230000037029 cross reaction Effects 0.000 description 1
- 210000004748 cultured cell Anatomy 0.000 description 1
- UQHKFADEQIVWID-UHFFFAOYSA-N cytokinin Natural products C1=NC=2C(NCC=C(CO)C)=NC=NC=2N1C1CC(O)C(CO)O1 UQHKFADEQIVWID-UHFFFAOYSA-N 0.000 description 1
- 239000004062 cytokinin Substances 0.000 description 1
- 230000009089 cytolysis Effects 0.000 description 1
- 210000000805 cytoplasm Anatomy 0.000 description 1
- 231100000135 cytotoxicity Toxicity 0.000 description 1
- 230000003013 cytotoxicity Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000012217 deletion Methods 0.000 description 1
- 230000037430 deletion Effects 0.000 description 1
- 210000000852 deltoid muscle Anatomy 0.000 description 1
- 210000004443 dendritic cell Anatomy 0.000 description 1
- 238000000432 density-gradient centrifugation Methods 0.000 description 1
- 238000001784 detoxification Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000003745 diagnosis Methods 0.000 description 1
- 238000002405 diagnostic procedure Methods 0.000 description 1
- UMGXUWVIJIQANV-UHFFFAOYSA-M didecyl(dimethyl)azanium;bromide Chemical compound [Br-].CCCCCCCCCC[N+](C)(C)CCCCCCCCCC UMGXUWVIJIQANV-UHFFFAOYSA-M 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 229960003983 diphtheria toxoid Drugs 0.000 description 1
- 150000002016 disaccharides Chemical class 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 238000001962 electrophoresis Methods 0.000 description 1
- 230000013020 embryo development Effects 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 230000012202 endocytosis Effects 0.000 description 1
- 210000002472 endoplasmic reticulum Anatomy 0.000 description 1
- 210000001163 endosome Anatomy 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 229960003276 erythromycin Drugs 0.000 description 1
- 229940105423 erythropoietin Drugs 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000262 estrogen Substances 0.000 description 1
- 229940011871 estrogen Drugs 0.000 description 1
- 210000003527 eukaryotic cell Anatomy 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 229960000304 folic acid Drugs 0.000 description 1
- 235000019152 folic acid Nutrition 0.000 description 1
- 239000011724 folic acid Substances 0.000 description 1
- 229940044627 gamma-interferon Drugs 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003862 glucocorticoid Substances 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 102000006602 glyceraldehyde-3-phosphate dehydrogenase Human genes 0.000 description 1
- 210000003958 hematopoietic stem cell Anatomy 0.000 description 1
- 206010073071 hepatocellular carcinoma Diseases 0.000 description 1
- 231100000844 hepatocellular carcinoma Toxicity 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 1
- 239000012510 hollow fiber Substances 0.000 description 1
- 229930186900 holotoxin Natural products 0.000 description 1
- 244000052637 human pathogen Species 0.000 description 1
- 230000001900 immune effect Effects 0.000 description 1
- 229940042743 immune sera Drugs 0.000 description 1
- 210000000987 immune system Anatomy 0.000 description 1
- 230000000984 immunochemical effect Effects 0.000 description 1
- 238000001114 immunoprecipitation Methods 0.000 description 1
- 230000004957 immunoregulator effect Effects 0.000 description 1
- 239000003022 immunostimulating agent Substances 0.000 description 1
- 230000002779 inactivation Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 description 1
- 239000000411 inducer Substances 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 230000002458 infectious effect Effects 0.000 description 1
- 206010022000 influenza Diseases 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229940047124 interferons Drugs 0.000 description 1
- 229940047122 interleukins Drugs 0.000 description 1
- 238000004255 ion exchange chromatography Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 229960000318 kanamycin Drugs 0.000 description 1
- 229930027917 kanamycin Natural products 0.000 description 1
- SBUJHOSQTJFQJX-NOAMYHISSA-N kanamycin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CN)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](N)[C@H](O)[C@@H](CO)O2)O)[C@H](N)C[C@@H]1N SBUJHOSQTJFQJX-NOAMYHISSA-N 0.000 description 1
- 229930182823 kanamycin A Natural products 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 101150066555 lacZ gene Proteins 0.000 description 1
- 229940039696 lactobacillus Drugs 0.000 description 1
- 235000021374 legumes Nutrition 0.000 description 1
- 208000032839 leukemia Diseases 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 210000001165 lymph node Anatomy 0.000 description 1
- 210000004698 lymphocyte Anatomy 0.000 description 1
- 210000003712 lysosome Anatomy 0.000 description 1
- 230000001868 lysosomic effect Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 235000005739 manihot Nutrition 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 101150095079 menB gene Proteins 0.000 description 1
- 229940014135 meningitis vaccine Drugs 0.000 description 1
- 208000037941 meningococcal disease Diseases 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 150000002772 monosaccharides Chemical class 0.000 description 1
- 229940031348 multivalent vaccine Drugs 0.000 description 1
- 230000035772 mutation Effects 0.000 description 1
- 201000000050 myeloid neoplasm Diseases 0.000 description 1
- 229960004927 neomycin Drugs 0.000 description 1
- 108091027963 non-coding RNA Proteins 0.000 description 1
- 102000042567 non-coding RNA Human genes 0.000 description 1
- 230000004942 nuclear accumulation Effects 0.000 description 1
- 101150087557 omcB gene Proteins 0.000 description 1
- 101150115693 ompA gene Proteins 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 229960005030 other vaccine in atc Drugs 0.000 description 1
- 210000001672 ovary Anatomy 0.000 description 1
- 238000012261 overproduction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000007030 peptide scission Effects 0.000 description 1
- 210000001322 periplasm Anatomy 0.000 description 1
- 108010021711 pertactin Proteins 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 229940127557 pharmaceutical product Drugs 0.000 description 1
- 210000003800 pharynx Anatomy 0.000 description 1
- 101150009573 phoA gene Proteins 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- WTJKGGKOPKCXLL-RRHRGVEJSA-N phosphatidylcholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCCCCCCCC WTJKGGKOPKCXLL-RRHRGVEJSA-N 0.000 description 1
- 150000008104 phosphatidylethanolamines Chemical class 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 230000026731 phosphorylation Effects 0.000 description 1
- 238000006366 phosphorylation reaction Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 210000000745 plant chromosome Anatomy 0.000 description 1
- 239000003375 plant hormone Substances 0.000 description 1
- 230000037039 plant physiology Effects 0.000 description 1
- 235000021118 plant-derived protein Nutrition 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 229920000724 poly(L-arginine) polymer Polymers 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 108010011110 polyarginine Proteins 0.000 description 1
- 239000004633 polyglycolic acid Substances 0.000 description 1
- 239000004626 polylactic acid Substances 0.000 description 1
- 108010055896 polyornithine Proteins 0.000 description 1
- 229920002714 polyornithine Polymers 0.000 description 1
- 230000004481 post-translational protein modification Effects 0.000 description 1
- 230000001124 posttranscriptional effect Effects 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940070353 protamines Drugs 0.000 description 1
- 235000019833 protease Nutrition 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000000164 protein isolation Methods 0.000 description 1
- 229940023143 protein vaccine Drugs 0.000 description 1
- 230000006337 proteolytic cleavage Effects 0.000 description 1
- 230000005180 public health Effects 0.000 description 1
- 239000002510 pyrogen Substances 0.000 description 1
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 1
- 108020003175 receptors Proteins 0.000 description 1
- 102000005962 receptors Human genes 0.000 description 1
- 238000010188 recombinant method Methods 0.000 description 1
- 230000003362 replicative effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 238000010845 search algorithm Methods 0.000 description 1
- 230000003248 secreting effect Effects 0.000 description 1
- 238000012163 sequencing technique Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000002741 site-directed mutagenesis Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 229940063673 spermidine Drugs 0.000 description 1
- 229940063675 spermine Drugs 0.000 description 1
- 210000000952 spleen Anatomy 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 150000003431 steroids Chemical class 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 230000001502 supplementing effect Effects 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 229940037128 systemic glucocorticoids Drugs 0.000 description 1
- 229960000814 tetanus toxoid Drugs 0.000 description 1
- 229940104230 thymidine Drugs 0.000 description 1
- 229940036555 thyroid hormone Drugs 0.000 description 1
- 239000005495 thyroid hormone Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 238000011426 transformation method Methods 0.000 description 1
- 230000009261 transgenic effect Effects 0.000 description 1
- 230000014621 translational initiation Effects 0.000 description 1
- 101150035767 trp gene Proteins 0.000 description 1
- 101150044170 trpE gene Proteins 0.000 description 1
- 210000004881 tumor cell Anatomy 0.000 description 1
- ZHSGGJXRNHWHRS-VIDYELAYSA-N tunicamycin Chemical compound O([C@H]1[C@@H]([C@H]([C@@H](O)[C@@H](CC(O)[C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C(NC(=O)C=C2)=O)O)O1)O)NC(=O)/C=C/CC(C)C)[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1NC(C)=O ZHSGGJXRNHWHRS-VIDYELAYSA-N 0.000 description 1
- MEYZYGMYMLNUHJ-UHFFFAOYSA-N tunicamycin Natural products CC(C)CCCCCCCCCC=CC(=O)NC1C(O)C(O)C(CC(O)C2OC(C(O)C2O)N3C=CC(=O)NC3=O)OC1OC4OC(CO)C(O)C(O)C4NC(=O)C MEYZYGMYMLNUHJ-UHFFFAOYSA-N 0.000 description 1
- 238000005199 ultracentrifugation Methods 0.000 description 1
- 241001529453 unidentified herpesvirus Species 0.000 description 1
- 230000003827 upregulation Effects 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 108700026220 vif Genes Proteins 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000003260 vortexing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/02—Bacterial antigens
- A61K39/095—Neisseria
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/20—Antivirals for DNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/54—Medicinal preparations containing antigens or antibodies characterised by the route of administration
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
- A61K2039/55505—Inorganic adjuvants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/60—Medicinal preparations containing antigens or antibodies characteristics by the carrier linked to the antigen
- A61K2039/6031—Proteins
- A61K2039/6068—Other bacterial proteins, e.g. OMP
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/70—Multivalent vaccine
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Immunology (AREA)
- Virology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Mycology (AREA)
- Microbiology (AREA)
- Molecular Biology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Biotechnology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Peptides Or Proteins (AREA)
- Medicinal Preparation (AREA)
Description
本発明は、Neisseria meningitidis血清型B(NmB)に対するワクチンに関する。
Neisseria meningitidisは、非運動性のグラム陰性双球菌ヒト病原体である。これは、咽頭にコロニー形成をし、髄膜炎(および、時折、髄膜炎のない敗血症)を引き起こす。米国において、発病率は1年間に100、000人あたり0.6〜1人の割合であり、そして大流行によりずっと大きくなり得る(Liebermanら(1996)JAMA 275(19):1499−1503;Schuchatら(1997)N Engl J Med 377(14):970−976)。発展途上国では、風土病の割合はずっと大きく、そして流行の間、発生率は1年間あたり100、000人あたり500症例に達し得る。死亡率は極めて高く、米国では10〜20%、そして発展途上国においてはよりずっと高い。Haemophilus influenzaeに対する結合ワクチンの導入後、N.meningitidisは、米国において全ての年齢における細菌性髄膜炎の主な原因である(Schuchatら(1997)前出)。
驚くべきことに、OMVワクチンへの規定された成分のさらなる添加が、それらの効果を有意に拡大することが見出された。
・WO99/57280に開示されるタンパク質またはその免疫原性フラグメント;
・WO99/36544に開示されるタンパク質またはその免疫原性フラグメント;
・WO99/24578に開示されるタンパク質またはその免疫原性フラグメント;
・WO00/66791に開示されるタンパク質またはその免疫原性フラグメント;
・Tettelinら[Science(2000)287:1809-1815]に開示されるタンパク質またはその免疫原性フラグメント;
・Parkhillら[Nature(2000)404:502−506]に開示されるタンパク質またはその免疫原性フラグメント;
・WO97/28273に開示されるタンパク質またはその免疫原性フラグメント;
・WO96/29412に開示されるタンパク質またはその免疫原性フラグメント;
・WO95/03413に開示されるタンパク質またはその免疫原性フラグメント;
・WO99/31132に開示されるタンパク質またはその免疫原性フラグメント;
・WO99/58683に開示されるタンパク質またはその免疫原性フラグメント;
・WO99/55873に開示されるタンパク質またはその免疫原性フラグメント;
・Neisseria meningitidisタンパク質PorA、TbpA、TbpB、PilC、OpA、またはOmp85。
・WO99/57280の配列番号3069〜3074および3207〜3241に代表されるタンパク質「919」(その中の図23および実施例15もまた参照のこと);
・WO99/57280の配列番号869〜874および3149〜3178に代表されるタンパク質「235」(その中の図20および実施例12もまた参照のこと);
・WO99/57280の配列番号3045〜3056および3185〜3206に代表されるタンパク質「519」(その中の図22および実施例14もまた参照のこと);
・WO99/57280の配列番号793〜804および3115〜3148に代表されるタンパク質「225」(その中の図19および実施例11もまた参照のこと);
・WO99/36544の実施例1(配列番号1〜6)に代表されるタンパク質「ORF40」(WO00/66741の図1もまた参照のこと;WO99/31132およびWO99/58683もまた参照のこと);
・WO99/57280の実施例9に代表されるタンパク質「287」(その中の配列番号1199〜1204、3103〜3108、および3179〜3184を参照のこと);
・WO99/24578の実施例77(配列番号647〜654)に代表されるタンパク質「ORF1」(WO99/55873および登録番号AJ242535もまた参照のこと);
・WO99/24578の実施例26(配列番号215〜226)に代表されるタンパク質「ORF4」(WO00/66741の図2もまた参照のこと);
・WO99/24578の実施例55(配列番号457〜466)に代表されるタンパク質「ORF46」(WO00/66741の図12もまた参照のこと)。
例えば、本発明は以下を提供する。
(項目1) (a)N.meningitidis血清型B外膜調製物、および(b)以下の1つ以上から選択される免疫原性成分を含む、組成物:
・WO99/57280に開示されるタンパク質、またはその免疫原性フラグメント;
・WO99/36544に開示されるタンパク質、またはその免疫原性フラグメント;
・WO99/24578に開示されるタンパク質、またはその免疫原性フラグメント;
・WO00/66791に開示されるタンパク質、またはその免疫原性フラグメント;
・Tettelinら[Science(2000)287:1809-1815]に開示されるタンパク質、またはその免疫原性フラグメント;
・WO97/28273に開示されるタンパク質、またはその免疫原性フラグメント;
・WO96/29412に開示されるタンパク質、またはその免疫原性フラグメント;
・WO95/03413に開示されるタンパク質、またはその免疫原性フラグメント;
・WO99/31132に開示されるタンパク質、またはその免疫原性フラグメント;
・WO99/58683に開示されるタンパク質、またはその免疫原性フラグメント;
・WO99/55873に開示されるタンパク質、またはその免疫原性フラグメント;
・Neisseria meningitidisタンパク質PorA、TbpA、TbpB、PilC、OpA、Omp85。
(項目2) 項目1に記載の組成物であって、前記成分(b)がNmBタンパク質である、組成物。
(項目3) 項目2に記載の組成物であって、前記NmBタンパク質が、タンパク質919、タンパク質235、タンパク質519、タンパク質225、タンパク質ORF40、タンパク質287、ORF1、ORF4、またはORF46である、組成物。
(項目4) 項目1〜3のいずれかに記載の組成物であって、前記成分(b)が、前記成分(a)が由来するNmB株とは異なる株に由来するタンパク質を含む、組成物。
(項目5) 項目1〜4のいずれかに記載の組成物であって、前記成分の1つ以上がAl(OH)3に吸着される、組成物。
(項目6) 項目1〜5のいずれかに記載の組成物であって、前記成分(a)がOMVを含む、組成物。
(項目7) 項目6に記載の組成物であって、前記OMVが、NmB由来のデオキシコレート抽出物である、組成物。
(項目8) 項目1〜7のいずれかに記載の組成物であって、前記成分(a)がAl(OH)3に吸着される、組成物。
(項目9) 項目1〜8のいずれかに記載の組成物であって、該組成物が、以下の成分の1つ以上をさらに含む、組成物:
・Neisseria meningitidis血清型Aに対する防御抗原;
・Neisseria meningitidis血清型Cに対する防御抗原;
・Neisseria meningitidis血清型Yに対する防御抗原;
・Neisseria meningitidis血清型Wに対する防御抗原;
・Haemophilus influenzaeに対する防御抗原;
・pneumococcusに対する防御抗原;
・ジフテリアに対する防御抗原;
・破傷風に対する防御抗原;
・百日咳に対する防御抗原;
・Helicobacter pyloriに対する防御抗原;
・ポリオに対する防御抗原;および/または
・B型肝炎ウイルスに対する防御抗原。
(項目10) 前記組成物がワクチンである、項目1〜9のいずれかに記載の組成物。
(項目11) 医薬品として使用されるための、項目1〜10のいずれかに記載の組成物。
(項目12) 以下の(i)、(ii)および/または(iii)の製造における項目1〜11のいずれかに記載の組成物の使用。(i)Neisseria細菌に起因する感染を処置または防止するための医薬品;(ii)Neisseria細菌の存在またはNeisseria細菌に対して惹起された抗体の存在を検出するための診断試薬;(iii)Neisseria細菌に対する抗体を惹起し得る試薬。
(項目13) 患者の処置方法であって、項目1〜10のいずれか1項に記載の組成物の治療有効量を患者に投与する工程を包含する、方法。
(項目14) 以下の1つ以上から選択される免疫原性成分を含む、細菌外膜調製物:
・WO99/57280に開示されるタンパク質、またはその免疫原性フラグメント;
・WO99/36544に開示されるタンパク質、またはその免疫原性フラグメント;
・WO99/24578に開示されるタンパク質、またはその免疫原性フラグメント;
・WO00/66791に開示されるタンパク質、またはその免疫原性フラグメント;
・Tettelinら[Science(2000)287:1809-1815]に開示されるタンパク質、またはその免疫原性フラグメント;
・WO97/28273に開示されるタンパク質、またはその免疫原性フラグメント;
・WO96/29412に開示されるタンパク質、またはその免疫原性フラグメント;
・WO95/03413に開示されるタンパク質、またはその免疫原性フラグメント;
・WO99/31132に開示されるタンパク質、またはその免疫原性フラグメント;
・WO99/58683に開示されるタンパク質、またはその免疫原性フラグメント;
・WO99/55873に開示されるタンパク質、またはその免疫原性フラグメント;ならびに/あるいは
・Neisseria meningitidisタンパク質PorA、TbpA、TbpB、PilC、OpA、Omp85。
本発明の組成物は、NmB外膜調製物(成分(a))を含む。これは、膜小胞(OMV)の形態が好ましい。
成分(a)と(b)は、単純に成分(a)と外膜調製物を混合することにより(例えば、ORF4とノルウェーOMVを混合することにより)配合され得る。
必要に応じて、本発明の組成物はまた、以下の成分の1つ以上を含み得る:
・Neisseria meningitidis血清型Aに対する防御抗原;
・Neisseria meningitidis血清型Cに対する防御抗原;
・Neisseria meningitidis血清型Yに対する防御抗原;
・Neisseria meningitidis血清型Wに対する防御抗原;
・Haemophilus influenzaeに対する防御抗原;
・pneumococcusに対する防御抗原;
・ジフテリアに対する防御抗原;
・破傷風に対する防御抗原;
・百日咳に対する防御抗原;
・Helicobacter pyloriに対する防御抗原;
・ポリオに対する防御抗原;および/または
・B型肝炎ウイルスに対する防御抗原。
・Neisseria meningitidis血清型Aに対する多糖類抗原;
・Neisseria meningitidis血清型Cに対する多糖類抗原(例えば、Costantinoら(1992)Vaccine 10:691-698);
・Neisseria meningitidis血清型Yに対する多糖類抗原;
・Neisseria meningitidis血清型Wに対する多糖類抗原;
・Haemophilus influenzaeに対する多糖類抗原;
・pneumococcusに対する多糖類抗原;
・ジフテリアトキソイド(例えば、CRM197変異体[例えば、Del Guidiceら(1998)Molecular Aspects of Medicine 19:1-70])からなる、ジフテリアに対する防御抗原;
・破傷風トキソイド[例えば、WassilakおよびOrenstein、Vaccinesの第4章(PlotkinおよびMortimer編)、1988]からなる、破傷風に対する防御抗原;
・百日咳ホロトキシン(pertussis holotoxin)(PT)および糸状血球凝集素(filamentous haemagglutinin)(FHA)を含む;必要に応じてパータクチン(pertactin)および/または凝集原2および3[例えば、Gustafssonら(1996)N.Engl.J.Med.334:349-355;Rappuoliら(1991)TIBTECH9:232-238]をさらに含む、百日咳に対する防御抗原;
・CagA(例えば、WO93/18150)、VacA(例えば、WO93/19150)、NAP(例えば、WO99/53310)、HopX(例えば、WO98/04702)、HopY(例えば、WO98/04702)、ウレアーゼの1つ以上を含む、H.pyloriに対する防御抗原;
・HBV表面抗原および/またはHBVコア抗原からなる、B型肝炎ウイルスに対する防御抗原。
本発明の組成物は、好ましくはワクチンである。本発明に基づくワクチンは、予防的(すなわち感染を防止する)であるか、または治療的(すなわち、感染後の疾患を処置する)であるかのいずれかであり得る。
さらなる局面によれば、本発明は、種々のプロセスを提供する。
この配列表における配列は以下のようなものである。
本発明を実行するために用いられ得る標準的な技術および手順(例えば、ワクチン接種目的または診断目的のために、開示された配列を利用するための)の要旨は以下の通りである。この要旨は、本発明に対する限定ではなく、むしろ使用され得るが必ずしもそうではない例を与えるものである。
本発明の実施は、他に示されなければ、分子生物学、微生物学、組換えDNA、および免疫学の従来技術を使用し、これらは当該分野の技術の範囲内である。このような技術は以下の文献で十分説明されている(例えば、Sambrook Molecular Cloning;A Laboratory Manual、第2版(1989);DNA Cloning、Volumes I and ii(D.N Glover編 1985);Oligonucleotide Synthesis(M.J.Gait編 1984);Nucleic Acid Hybridization(B.D.HamesおよびS.J.Higgins編 1984);Transcription and Translation(B.D.HamesおよびS.J.Higgins編 1984);Animal Cell Culture(R.I.Freshney編 1986);Immobilized Cells and Enzymes(IRL Press、1986);B.Perbal、A Practial Guide to Molecular Cloning(1984);the Methods in Enzymology series(Academic Press、Inc.)、特に154巻および155巻;Gene Transfer Vectors for Mammalian Cells(J.H.MillerおよびM.P.Calos編1987、Cold Spring Harbor Laboratory);MayerおよびWalker、編(1987)、Immunochemical Methods in Cell and Molecular Biology(Academic Press、London);Scopes、(1987)Protein Purification:Principles and Practice、第2版(Springer−Verlag、N.Y.)、およびHandbook of Experimental Immunology、Volumes I−IV(D.M.WeirおよびC.C.Blackwell編 1986)。
Xを含む組成物は、組成物中のX+Yの合計のうちの少なくとも85重量%がXであるとき、Yを「実質的に含まない」。好ましくは、Xは、組成物中のX+Yの合計のうちの少なくとも約90重量%を、さらに好ましくは少なくとも約95重量%を、または99重量%さえも構成する。
ナイセリアヌクレオチド配列は、種々の異なる発現系;例えば、哺乳動物細胞、バキュロウイルス、植物、細菌、および酵母について使用される発現系において発現され得る。
哺乳動物発現系は当該分野において公知である。哺乳動物プロモーターは、哺乳動物RNAポリメラーゼを結合し得、コード配列(例えば、構造遺伝子)のmRNAへの下流(3’)転写を開始し得る任意のDNA配列である。プロモーターは、転写開始領域(これはコード配列の5’末端の近位に通常位置する)およびTATAボックス(転写開始部位の25〜30塩基対(bp)上流に通常位置する)を有する。TATAボックスは、RNAポリメラーゼIIにその正しい部位においてRNA合成を開始させるよう指示すると考えられている。哺乳動物プロモーターはまた、TATAボックスの100〜200bp上流以内に通常位置する上流プロモーターエレメントを含む。上流プロモーターエレメントは、転写が開始される速度を決定し、そしていずれの方向にも作用し得る(Sambrookら(1989)「Expression of Cloned Genes in Mammalian Cells.」、Molecular Cloning:A Laboratory Manual、第2版)。
タンパク質をコードするポリヌクレオチドはまた、適切な昆虫発現ベクター内に挿入され得、そしてそのベクター内で、制御エレメントに作動可能に連結される。ベクターの構築には、当該分野で公知の技術を使用する。一般に、その発現系の構成要素として、以下のものが挙げられる:バキュロウイルスゲノムのフラグメント、および発現させる異種遺伝子の挿入用の簡便な制限部位の両方を含む転移ベクター(通常は細菌プラスミド);転移ベクター内のバキュロウイルスに特異的なフラグメントに相同性のある配列を有する野生型バキュロウイルス(これは、バキュロウイルスゲノム内への異種遺伝子の相同組換えを可能にする);ならびに適切な昆虫宿主細胞および増殖培地。
当該分野で公知の多くの植物細胞培養および全植物遺伝子発現系が存在する。例示的な植物細胞遺伝子発現系としては、米国特許第5、693、506号;米国特許第5、659、122号;および米国特許第5、608、143号のような特許に記載されるものが挙げられる。植物細胞培養における遺伝子発現のさらなる例は、Zenk、Phytochemistry 30:3861−3863(1991)に記載された。植物タンパク質のシグナルペプチドの記載は、上記の参考文献に加え、以下に示すものの中においても見出され得る;Vaulcombeら、Mol.Gen.Genet.209:33−40(1987);Chandlerら、Plant Molecular Biology 3:407−418(1984);Rogers、J.Biol.Chem.260:3731−3738(1985);Rothsteinら、Gene 55:353−356(1987);Whittierら、Nucleic Acids Research 15:2515−2535(1987);Wirselら、Molecular Microbiology 3:3−14(1989);Yuら、Gene 122:247−253(1992)。植物ホルモンジベレリン酸およびジベレリン酸により誘導される分泌酵素による植物遺伝子発現の調節の記載は、R.L.JonesおよびJ.MacMillin、Gibberellins:Advanced Plant Physiology、Malcolm B.Wilkins編 1984 Pitman Publishing Limited、London、21−52頁の中に見出され得る。他の代謝調節性遺伝子が記載される参考文献:Sheen、Plant Cell、2:1027−1038(1990);Maasら、EMBO J.9:3447−3452(1990);BenkelおよびHickey、Proc.Natl.Acad.Sci.84:1337−1339(1987)。
細菌の発現技術は、当該分野で公知である。細菌のプロモーターは、細菌のRNAポリメラーゼに結合し得そしてコード配列(例えば、構造遺伝子)の下流方向(3’方向)へのmRNAへの転写を開始し得る、任意のDNA配列である。プロモーターは、通常、コード配列の5’末端に近接して配置される、転写開始領域を有する。この転写開始領域は、通常、RNAポリメラーゼ結合部位および転写開始部位を含む。細菌のプロモーターはまた、オペレーターと呼ばれる第二のドメインを有し、これは、RNA合成が開始する、隣接するRNAポリメラーゼ結合部位と重複し得る。オペレーターは、遺伝子リプレッサータンパク質がこのオペレーターに結合し、それによって、特定の遺伝子の転写を阻害し得るような、負の調節された(誘導性の)転写を可能にする。構成的発現は、オペレーターのような負の調節エレメントの非存在下で起こり得る。さらに、正の調節は、遺伝子アクチベータータンパク質結合配列により達成され得、この配列は、通常、存在する場合には、RNAポリメラーゼ結合配列の(5’)側に近接している。遺伝子アクチベータータンパク質の例としては、カタボライト活性化タンパク質(CAP)があり、これは、Escherichia coli(E.coli)におけるlacオペロンの転写の開始を補助する(Raibaudら(1984)Annu.Rev.Genet.18:173)。従って、調節される発現は、正または負のいずれかであり、それによって、転写を増強するかまたは低下し得る。
酵母発現系もまた、当業者に公知である。酵母プロモーターは、酵母RNAポリメラーゼに結合し得そしてコード配列(例えば、構造遺伝子)からmRNAへの下流の(3’側の)転写を開始し得る、任意のDNA配列である。プロモーターは、通常、コード配列の5’末端の近位に位置する、転写開始領域を有する。この転写開始領域は、通常、RNAポリメラーゼ結合部位(「TATAボックス」)および転写開始部位を含む。酵母プロモーターはまた、上流アクチベーター配列(UAS)と呼ばれる第2のドメインを有し得、これは、存在する場合、通常、構造遺伝子に対して遠位にある。このUASは、調節された(誘導性)発現を可能にする。構成的発現は、UASの非存在下で生じる。調節された発現は、正または負のいずれかであり得、それによって、転写を増強または減少させ得る。
本明細書中で使用される場合、用語「抗体」とは、少なくとも1つの抗体結合部位から構成されるポリペプチドまたはポリペプチド群をいう。「抗体結合部位」は、内部表面形状および抗原のエピトープの特徴に相補的な電荷分布を有する、3次元結合空間であり、これが、抗体と抗原の結合を可能にする。「抗体」は、例えば、脊椎動物抗体、ハイブリッド抗体、キメラ抗体、ヒト化抗体、改変された抗体、単価抗体、Fabタンパク質、および単一ドメイン抗体を含む。
薬学的組成物は、本発明のポリペプチド、抗体または核酸のいずれかを含み得る。この薬学的組成物は、治療上有効な量の、本願発明のポリペプチド、抗体、またはポリヌクレオチドのいずれかを含む。
一旦処方されると、本発明の組成物は、その被験体へ直接投与され得る。処置される被験体は、動物であり得;特に、ヒト被験体が処置され得る。
ワクチンは、免疫抗原、免疫原、ポリペプチド、タンパク質または核酸を、通常「薬学的に受容可能なキャリア」とともに含み、このキャリアは、その組成物を受ける個体に有害である抗体の産生をそれ自体は誘発しない任意のキャリアを含む。適切なキャリアは、代表的に、大きく、ゆっくり代謝される高分子(例えば、タンパク質、多糖、ポリ乳酸、ポリグリコール酸、重合アミノ酸、アミノ酸コポリマー、脂質凝集物(例えば、油小滴またはリポソーム)、および不活性ウイルス粒子である。このようなキャリアは、当業者に周知である。さらに、これらのキャリアは免疫刺激薬剤(「アジュバント」)として機能し得る。さらに、この抗原または免疫原は、細菌毒素(例えば、ジフテリア、破傷風、コレラ、H.pyloriなどの病原体由来の毒素)と結合体化され得る。
本発明の治療剤のコード配列を含む、哺乳動物における発現のためにその哺乳動物へ送達される構築物の送達のための遺伝子治療ビヒクルは、局所または全身的のいずれかで投与され得る。これらの構築物は、ウイルスベクターアプローチまたは非ウイルスベクターアプローチを、インビボまたはエキソビボの様式で利用し得る。このようなコード配列の発現は、内因性哺乳動物プロモーターまたは外因性プロモーターを用いて誘導され得る。このコード配列のインビボでの発現は、構成性または調節性のいずれかであり得る。
一旦処方されると、本発明のポリヌクレオチド組成物は、(1)被験体に直接);(2)エキソビボで被験体由来の細胞に送達されて;または(3)組換えタンパク質の発現のためにインビトロで、投与され得る。処置される被験体は、哺乳動物または鳥類であり得る。ヒト被験体もまた処置され得る。
上記に記載の薬学的に受容可能なキャリアおよび塩に加えて、以下のさらなる薬剤がポリヌクレオチド組成物および/またはポリペプチド組成物とともに使用され得る。
1つの例は、限定することなく以下を包含するポリペプチドである:アシアロオロソムコイド(ASOR);トランスフェリン;アシアロ糖タンパク質;抗体;抗体フラグメント;フェリチン;インターロイキン;インターフェロン;顆粒球マクロファージコロニー刺激因子(GM−CSF)、顆粒球コロニー刺激因子(G−CSF)、マクロファージコロニー刺激因子(M−CSF)、幹細胞因子およびエリスロポエチン。ウイルス抗原(例えば、エンベロープタンパク質)もまた、使用され得る。また、他の侵襲性生物由来のタンパク質(例えば、RIIとして知られる熱帯熱マラリア原虫(plasmodium falciparum)のサーカムスポロゾイト(circumsporozoite)タンパク質由来の17アミノ酸ペプチド)。
包含され得る他の群は、例えば、ホルモン、ステロイド、アンドロゲン、エストロゲン、甲状腺ホルモン、またはビタミン、葉酸である。
また、ポリアルキレングリコールが、所望のポリヌクレオチド/ポリペプチドとともに含まれ得る。好ましい実施態様において、ポリアルキレングリコールは、ポリエチレングリコールである。さらに、モノサッカリド、ジサッカリド、またはポリサッカリドが含有され得る。この局面の好ましい実施態様において、このポリサッカリドは、デキストランまたはDEAE−デキストランである。また、キトサンおよびポリ(乳酸−コ−グリコリド)
(D.脂質およびリポソーム)
所望のポリヌクレオチド/ポリペプチドはまた、被験体またはそれに由来する細胞への送達の前に、脂質中にカプセル化され得るか、またはリポソーム中にパッケージングされ得る。
さらに、リポタンパク質が、送達されるポリヌクレオチド/ポリペプチドと共に含まれ得る。利用されるリポタンパク質の例としては、カイロミクロン、HDL、IDL、LDL、およびVLDLが挙げられる。これらのタンパク質の変異体、フラグメント、または融合物もまた、使用され得る。また、天然に存在するリポタンパク質の改変体(例えば、アセチル化されたLDL)が使用され得る。これらのリポタンパク質は、リポタンパク質レセプターを発現する細胞へのポリヌクレオチドの送達を標的化し得る。好ましくは、リポタンパク質が、送達されるポリヌクレオチドと共に含まれる場合、他の標的化リガンドはその組成物中には含まれない。
ポリカチオン性薬剤は、送達される所望のポリヌクレオチド/ポリペプチドを含む組成物中に、リポタンパク質を伴ってかまたはリポタンパク質を伴わずに含まれ得る。
本発明のNeisseria MenB抗原またはその抗原性フラグメントは、抗体レベルを検出するためのイムノアッセイにおいて使用され得る(または、逆に抗Neisseria抗体は抗原レベルを検出するために使用され得る)。十分に規定された組換え抗原に基づくイムノアッセイは、侵襲性の診断方法と置き換えるために開発され得る。生物学的サンプル(例えば、血液サンプルまたは血清サンプルを含む)内のNeisseria MenBタンパク質またはそのフラグメントに対する抗体が検出され得る。このイムノアッセイの設計は、多くのバリエーションの対象であり、そして種々のこれらは当該分野で公知である。イムノアッセイのプロトコルは、例えば、競合アッセイ、または直接反応アッセイ、またはサンドイッチ型アッセイに基づき得る。プロトコルはまた、例えば、固体支持体を使用し得、または免疫沈降によってなされ得る。ほとんどのアッセイは、標識された抗体またはポリペプチドの使用を含み、その標識は、例えば、蛍光分子、化学発光分子、放射性分子、または色素分子であり得る。プローブからのシグナルを増幅するアッセイは公知である;これらの例は、ビオチンおよびアビジンを利用するアッセイ、ならびに酵素標識および酵素媒介イムノアッセイ(例えば、ELASAアッセイ)である。
「ハイブリダイゼーション」とは、水素結合による2つの核酸配列の互いに対する会合をいう。代表的には、1つの配列は、固体支持体に固定され、そして他方は溶液中で遊離している。次いで、2つの配列は水素結合に好ましい条件下で互いに接触される。この結合に影響を与える因子としては以下が挙げられる:溶媒のタイプおよび容量;反応温度;ハイブリダイゼーションの時間;撹拌;液体相の配列の固体支持体への非特異的な付着をブロックする薬剤(Denhardt’s試薬またはBLOTTO);配列の濃度;配列の会合の速度を増大させる化合物(硫酸デキストランまたはポリエチレングリコール)の使用;およびハイブリダイゼーション後の洗浄条件のストリンジェンシー。Sambrookら(前出)第2巻、第9章、9.47〜9.57頁を参照のこと。
Tm=81+16.6(log10Ci)+0.4[%(G+C)]−0.6(%ホルムアミド)−600/n−1.5(%ミスマッチ)。
ここでCiは塩濃度(一価イオン)であり、そして塩基対内のハイブリッドの長さである(MeinkothおよびWahl(1984)Anal.Biochem.138:267/284からわずかに改変した)。
N.meningitidis血清型B由来の種々の外膜の小胞調製物は、約80〜85kDaの成分を含んでいたことが観察された。このタンパク質を、SDS−PAGEゲルから精製し、そしてN末端を配列決定した(配列番号1)。
血清型BのN.meningitidis配列に基づいて、N.meningitidis血清型AおよびN.gonorrhoeae由来の対応する遺伝子をクローン化し、そして配列決定した(「ORF」と称される)。
これらのタンパク質の配列を比較した。これらの配列は、高度に相同である。
上記のように同定されたこれらのタンパク質を発現させ、そして免疫化のために使用する。良好な免疫応答が、このタンパク質に対して観察される。
さらに、このタンパク質を、他の病原性生物に対する抗原とそれぞれ配合し(例えば、血清型Cのmeningitisに対してカイロンポリサッカリドワクチン)、そして免疫化のために使用した。良好な免疫応答が観察された。
ノルウェーOMVワクチン(Norwegian OMV vaccine)によって誘導される防御は、効果的であるが、そのワクチンを作製するために用いられた株に限定される。このワクチンについての臨床試験は、10代のヒトにおいて29月後では57.2%の有効性を獲得したのみであったが、IgG応答は、ほぼ100%の患者で観察された[例えば、Rosenqvistら(1995)Infect.Immun.63:4642−4652]。
−任意の融合パートナーなしにE.coliにおいて発現させた、タンパク質919
−Hisタグ融合体としてE.coliにおいて発現させた、ORF1
−GST融合体としてE.coliにおいて発現させた、タンパク質287
−これら3つのタンパク質の混合物(必要に応じてNmC結合体を有する)。
ノルウェーOMVと抗原287との配合物を、さらに調査した。20μgの抗原287をノルウェーOMPワクチン(15μg OMP+Al(OH)3)と配合し、そしてマウスを免疫するために用いた。抗体を殺菌アッセイにおいて試験した。そして、この抗体は、試験された全ての株に対して有効であった。この結果は、以下の通りであった。
E.coliを形質転換し、ORF1、ORF40、およびORF46を発現させた。組み換えE.coliから調製されたOMVは、N.meningitidisに対する殺菌性抗体を誘導し得た。
Claims (12)
- 請求項1に記載の組成物であって、前記成分(b)がNmBタンパク質である、組成物。
- 請求項1〜2のいずれか1項に記載の組成物であって、前記成分(b)が、前記成分(a)が由来する株とは異なるNmB株に由来するタンパク質を含む、組成物。
- 請求項1〜3のいずれか1項に記載の組成物であって、前記成分の1つ以上がAl(OH)3に吸着される、組成物。
- 請求項1〜4のいずれか1項に記載の組成物であって、前記成分(a)がOMVを含む、組成物。
- 請求項5に記載の組成物であって、前記OMVが、NmB由来のデオキシコレート抽出物である、組成物。
- 請求項1〜6のいずれか1項に記載の組成物であって、前記成分(a)がAl(OH)3に吸着される、組成物。
- 請求項1〜7のいずれか1項に記載の組成物であって、該組成物が、以下の成分の1つ以上をさらに含む、組成物:
・Neisseria meningitidis血清型Aに対する防御抗原;
・Neisseria meningitidis血清型Cに対する防御抗原;
・Neisseria meningitidis血清型Yに対する防御抗原;
・Neisseria meningitidis血清型Wに対する防御抗原;
・Haemophilus influenzaeに対する防御抗原;
・pneumococcusに対する防御抗原;
・ジフテリアに対する防御抗原;
・破傷風に対する防御抗原;
・百日咳に対する防御抗原;
・Helicobacter pyloriに対する防御抗原;
・ポリオに対する防御抗原;および/または
・B型肝炎ウイルスに対する防御抗原。 - 前記組成物がワクチンである、請求項1〜8のいずれか1項に記載の組成物。
- 医薬品として使用されるための、請求項1〜9のいずれか1項に記載の組成物。
- (i)Neisseria細菌に起因する感染の処置または防止;(ii)Neisseria細菌の存在またはNeisseria細菌に対して惹起された抗体の存在の検出;および(iii)Neisseria細菌に対する抗体の惹起からなる群より選択される目的のための、請求項1〜10のいずれか1項に記載の組成物。
- 患者の処置のための組成物であって、請求項1〜9のいずれか1項に記載の組成物の治療有効量を含む、組成物。
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0001067A GB0001067D0 (en) | 2000-01-17 | 2000-01-17 | Supplemented norwegian vaccine |
GB0001067.8 | 2000-01-17 | ||
GB0005699.4 | 2000-03-09 | ||
GBGB0005699.4A GB0005699D0 (en) | 2000-03-09 | 2000-03-09 | Supplemented OMV vaccines |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2011061748A Division JP2011116793A (ja) | 2000-01-17 | 2011-03-18 | N.meningitidis血清型b外膜タンパク質を含む外膜小胞(omv)ワクチン |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2015145631A Division JP2015193652A (ja) | 2000-01-17 | 2015-07-23 | N.meningitidis血清型b外膜タンパク質を含む外膜小胞(omv)ワクチン |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2013181035A JP2013181035A (ja) | 2013-09-12 |
JP5823446B2 true JP5823446B2 (ja) | 2015-11-25 |
Family
ID=26243421
Family Applications (6)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2001552932A Withdrawn JP2003520248A (ja) | 2000-01-17 | 2001-01-17 | N.meningitidis血清型b外膜タンパク質を含む外膜小胞(omv)ワクチン |
JP2011061748A Pending JP2011116793A (ja) | 2000-01-17 | 2011-03-18 | N.meningitidis血清型b外膜タンパク質を含む外膜小胞(omv)ワクチン |
JP2013124555A Pending JP2013181036A (ja) | 2000-01-17 | 2013-06-13 | N.meningitidis血清型b外膜タンパク質を含む外膜小胞(omv)ワクチン |
JP2013124554A Expired - Fee Related JP5823446B2 (ja) | 2000-01-17 | 2013-06-13 | N.meningitidis血清型b外膜タンパク質を含む外膜小胞(omv)ワクチン |
JP2013124556A Pending JP2013181037A (ja) | 2000-01-17 | 2013-06-13 | N.meningitidis血清型b外膜タンパク質を含む外膜小胞(omv)ワクチン |
JP2015145631A Pending JP2015193652A (ja) | 2000-01-17 | 2015-07-23 | N.meningitidis血清型b外膜タンパク質を含む外膜小胞(omv)ワクチン |
Family Applications Before (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2001552932A Withdrawn JP2003520248A (ja) | 2000-01-17 | 2001-01-17 | N.meningitidis血清型b外膜タンパク質を含む外膜小胞(omv)ワクチン |
JP2011061748A Pending JP2011116793A (ja) | 2000-01-17 | 2011-03-18 | N.meningitidis血清型b外膜タンパク質を含む外膜小胞(omv)ワクチン |
JP2013124555A Pending JP2013181036A (ja) | 2000-01-17 | 2013-06-13 | N.meningitidis血清型b外膜タンパク質を含む外膜小胞(omv)ワクチン |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2013124556A Pending JP2013181037A (ja) | 2000-01-17 | 2013-06-13 | N.meningitidis血清型b外膜タンパク質を含む外膜小胞(omv)ワクチン |
JP2015145631A Pending JP2015193652A (ja) | 2000-01-17 | 2015-07-23 | N.meningitidis血清型b外膜タンパク質を含む外膜小胞(omv)ワクチン |
Country Status (17)
Country | Link |
---|---|
US (4) | US8273360B2 (ja) |
EP (6) | EP2289545B1 (ja) |
JP (6) | JP2003520248A (ja) |
CN (2) | CN102172398A (ja) |
AT (1) | ATE476988T1 (ja) |
AU (2) | AU784518B2 (ja) |
BR (2) | BR0107679A (ja) |
CA (2) | CA2871789C (ja) |
CY (3) | CY1111056T1 (ja) |
DE (1) | DE60142772D1 (ja) |
DK (3) | DK2289545T3 (ja) |
ES (2) | ES2507100T3 (ja) |
MX (1) | MXPA02006962A (ja) |
NZ (1) | NZ520466A (ja) |
PT (3) | PT2289545T (ja) |
RU (1) | RU2279889C2 (ja) |
WO (1) | WO2001052885A1 (ja) |
Families Citing this family (116)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU1463097A (en) | 1996-01-04 | 1997-08-01 | Rican Limited | Helicobacter pylori bacterioferritin |
CA2266656A1 (en) | 1996-09-17 | 1998-03-26 | Chiron Corporation | Compositions and methods for treating intracellular diseases |
EP1093517B1 (en) | 1998-05-01 | 2008-03-05 | Novartis Vaccines and Diagnostics, Inc. | Neisseria meningitidis antigens and compositions |
US20070026021A1 (en) * | 1998-05-01 | 2007-02-01 | Chiron S.R.I. | Neisseria meningitidis antigens and compositions |
GB9823978D0 (en) * | 1998-11-02 | 1998-12-30 | Microbiological Res Authority | Multicomponent meningococcal vaccine |
US10967045B2 (en) * | 1998-11-02 | 2021-04-06 | Secretary of State for Health and Social Care | Multicomponent meningococcal vaccine |
AU2457100A (en) * | 1999-02-26 | 2000-09-14 | Chiron S.P.A. | Enhancement of bactericidal activity of neisseria antigens with oligonucleotidescontaining cg motifs |
NZ581940A (en) | 1999-04-30 | 2011-07-29 | Novartis Vaccines & Diagnostic | Conserved neisserial antigens |
NZ528254A (en) | 1999-05-19 | 2005-07-29 | Chiron S | Combined neisserial compositions |
PT2275553E (pt) | 1999-10-29 | 2015-09-18 | Glaxosmithkline Biolog Sa | Péptidos antigénicos de neisseria |
GB9928196D0 (en) | 1999-11-29 | 2000-01-26 | Chiron Spa | Combinations of B, C and other antigens |
BR0107679A (pt) * | 2000-01-17 | 2004-07-06 | Chiron Spa | Vacina de vesìcula de membrana externa (omv) compreendendo proteìnas de membrana externa do grupo sérico b de neisseria meningitidis |
WO2001064922A2 (en) | 2000-02-28 | 2001-09-07 | Chiron Spa | Heterologous expression of neisserial proteins |
BRPI0112928B1 (pt) | 2000-07-27 | 2017-08-29 | Children's Hospital & Research Center At Oakland | A composition comprising preparations comprising outer membrane vesicles (OMV), microvesicles (MV) or both MVO and MV |
GB0103170D0 (en) * | 2001-02-08 | 2001-03-28 | Smithkline Beecham Biolog | Vaccine composition |
JP4254931B1 (ja) | 2000-10-27 | 2009-04-15 | カイロン ソチエタ ア レスポンサビリタ リミタータ | A群連鎖球菌およびb群連鎖球菌由来の核酸およびタンパク質 |
GB0107658D0 (en) | 2001-03-27 | 2001-05-16 | Chiron Spa | Streptococcus pneumoniae |
GB0107661D0 (en) | 2001-03-27 | 2001-05-16 | Chiron Spa | Staphylococcus aureus |
GB0115176D0 (en) | 2001-06-20 | 2001-08-15 | Chiron Spa | Capular polysaccharide solubilisation and combination vaccines |
GB0118249D0 (en) | 2001-07-26 | 2001-09-19 | Chiron Spa | Histidine vaccines |
GB0121591D0 (en) | 2001-09-06 | 2001-10-24 | Chiron Spa | Hybrid and tandem expression of neisserial proteins |
US20050232936A1 (en) | 2001-07-27 | 2005-10-20 | Chiron Corporation | Meningococcus adhesins nada, app and orf 40 |
MX339524B (es) | 2001-10-11 | 2016-05-30 | Wyeth Corp | Composiciones inmunogenicas novedosas para la prevencion y tratamiento de enfermedad meningococica. |
EP2335724A1 (en) | 2001-12-12 | 2011-06-22 | Novartis Vaccines and Diagnostics S.r.l. | Immunisation against chlamydia trachomatis |
GB0130123D0 (en) | 2001-12-17 | 2002-02-06 | Microbiological Res Agency | Outer membrane vesicle vaccine and its preparation |
RU2359696C2 (ru) * | 2002-08-02 | 2009-06-27 | ГлаксоСмитКлайн Байолоджикалз с.а. | Вакцинная композиция, содержащая трансферрин-связывающий белок и hsf из грамотрицательных бактерий |
EP2481419A3 (en) | 2002-08-02 | 2013-04-10 | GlaxoSmithKline Biologicals S.A. | Neisserial vaccines |
GB0220194D0 (en) | 2002-08-30 | 2002-10-09 | Chiron Spa | Improved vesicles |
CA2501812C (en) | 2002-10-11 | 2012-07-10 | Mariagrazia Pizza | Polypeptide-vaccines for broad protection against hypervirulent meningococcal lineages |
MY132859A (en) | 2002-11-01 | 2007-10-31 | Glaxosmithkline Biologicals Sa | Immunogenic composition |
DK2279746T3 (da) | 2002-11-15 | 2013-11-25 | Novartis Vaccines & Diagnostic | Overfladeproteiner i neisseria meningitidis |
GB0227346D0 (en) | 2002-11-22 | 2002-12-31 | Chiron Spa | 741 |
US8034378B2 (en) | 2002-12-27 | 2011-10-11 | Novartis Vaccines And Diagnostics, Inc | Immunogenic compositions containing phospholipid |
CA2514328C (en) | 2003-01-30 | 2020-01-14 | Chiron Srl | Injectable vaccines against multiple meningococcal serogroups |
CA2520124A1 (en) | 2003-03-28 | 2004-10-14 | Chiron Corporation | Use of benzazole compounds for immunopotentiation |
GB0308198D0 (en) | 2003-04-09 | 2003-05-14 | Chiron Srl | ADP-ribosylating bacterial toxin |
DE602004022286D1 (de) | 2003-06-02 | 2009-09-10 | Novartis Vaccines & Diagnostic | Immunogene zusammensetzungen auf basis von biologisch abbaubaren mikroteilchen enthaltend ein diphtherie- und ein tetanustoxoid |
GB0323103D0 (en) | 2003-10-02 | 2003-11-05 | Chiron Srl | De-acetylated saccharides |
GB0406013D0 (en) | 2004-03-17 | 2004-04-21 | Chiron Srl | Analysis of saccharide vaccines without interference |
GB0408977D0 (en) | 2004-04-22 | 2004-05-26 | Chiron Srl | Immunising against meningococcal serogroup Y using proteins |
NZ550533A (en) * | 2004-04-30 | 2010-02-26 | Novartis Vaccines & Diagnostic | Meningococcal conjugate vaccination comprising N. meningitidis and diphtheria toxin |
GB0411387D0 (en) | 2004-05-21 | 2004-06-23 | Chiron Srl | Analysis of saccharide length |
GB0413868D0 (en) | 2004-06-21 | 2004-07-21 | Chiron Srl | Dimensional anlaysis of saccharide conjugates |
EP2277595A3 (en) | 2004-06-24 | 2011-09-28 | Novartis Vaccines and Diagnostics, Inc. | Compounds for immunopotentiation |
EP1768662A2 (en) | 2004-06-24 | 2007-04-04 | Novartis Vaccines and Diagnostics, Inc. | Small molecule immunopotentiators and assays for their detection |
WO2006078318A2 (en) | 2004-07-29 | 2006-07-27 | Novartis Vaccines And Diagnostics Inc. | Immunogenic compositions for gram positive bacteria such as streptococcus agalactiae |
GB0419408D0 (en) * | 2004-09-01 | 2004-10-06 | Chiron Srl | 741 chimeric polypeptides |
GB0424092D0 (en) | 2004-10-29 | 2004-12-01 | Chiron Srl | Immunogenic bacterial vesicles with outer membrane proteins |
NZ555937A (en) | 2005-01-27 | 2009-05-31 | Childrens Hosp & Res Ct Oak | GNA1870-based vesicle vaccines for broad spectrum protection against diseases caused by Neisseria meningitidis |
GB0502096D0 (en) | 2005-02-01 | 2005-03-09 | Chiron Srl | Purification of streptococcal capsular polysaccharide |
GB0502095D0 (en) | 2005-02-01 | 2005-03-09 | Chiron Srl | Conjugation of streptococcal capsular saccharides |
EP1945247A1 (en) | 2005-10-18 | 2008-07-23 | Novartis Vaccines and Diagnostics, Inc. | Mucosal and systemic immunizations with alphavirus replicon particles |
EP2360175B1 (en) | 2005-11-22 | 2014-07-16 | Novartis Vaccines and Diagnostics, Inc. | Norovirus and Sapovirus virus-like particles (VLPs) |
GB0524066D0 (en) | 2005-11-25 | 2006-01-04 | Chiron Srl | 741 ii |
GB0605757D0 (en) | 2006-03-22 | 2006-05-03 | Chiron Srl | Separation of conjugated and unconjugated components |
EP2010537B1 (en) | 2006-03-23 | 2011-12-28 | Novartis AG | Imidazoquinoxaline compounds as immunomodulators |
GB0700562D0 (en) | 2007-01-11 | 2007-02-21 | Novartis Vaccines & Diagnostic | Modified Saccharides |
GB0713880D0 (en) | 2007-07-17 | 2007-08-29 | Novartis Ag | Conjugate purification |
CA2695467A1 (en) * | 2007-08-02 | 2009-03-26 | Children's Hospital & Research Center At Oakland | Fhbp- and lpxl1-based vesicle vaccines for broad spectrum protection against diseases caused by neisseria meningitidis |
ES2561483T3 (es) | 2007-09-12 | 2016-02-26 | Glaxosmithkline Biologicals Sa | Antígenos mutantes de GAS57 y anticuerpos de GAS57 |
BRPI0818545A2 (pt) | 2007-10-19 | 2017-07-04 | Novartis Ag | formulações de vacinais meningocócicas |
JP5656642B2 (ja) | 2007-12-21 | 2015-01-21 | ノバルティス アーゲー | ストレプトリシンoの変異体形態 |
EP2886551A3 (en) | 2008-02-21 | 2015-09-23 | Novartis AG | Meningococcal fhbp polypeptides |
EA018068B1 (ru) | 2008-03-03 | 2013-05-30 | Айрм Ллк | Соединения и композиции в качестве модуляторов активности tlr |
WO2009158142A1 (en) * | 2008-05-30 | 2009-12-30 | The U.S.A., As Represented By The Secretary Of The Army, On Behalf Of Walter Reed Army | Meningococcal multivalent native outer membrane vesicle vaccine, methods of making and use thereof |
WO2010027499A2 (en) * | 2008-09-05 | 2010-03-11 | University Of Massachusetts Medical School | Methods, compositions and vaccines relating to neisseria meningitidis antibodies |
CA2777837C (en) | 2008-10-27 | 2017-07-11 | Novartis Ag | Purification method |
GB0822634D0 (en) | 2008-12-11 | 2009-01-21 | Novartis Ag | Meningitis vaccines |
JP2012512240A (ja) | 2008-12-17 | 2012-05-31 | ノバルティス アーゲー | ヘモグロビン受容体を含む髄膜炎菌ワクチン |
CN102307477B (zh) | 2009-01-05 | 2015-07-29 | 埃皮托吉尼西斯股份有限公司 | 佐剂组合物及使用方法 |
EP2385842A1 (en) | 2009-01-12 | 2011-11-16 | Novartis AG | Cna_b domain antigens in vaccines against gram positive bacteria |
DK2411048T3 (da) | 2009-03-24 | 2020-06-15 | Glaxosmithkline Biologicals Sa | Adjuvanterende meningokok-faktor h-bindingsprotein |
CN104650241A (zh) | 2009-08-27 | 2015-05-27 | 诺华股份有限公司 | 包括脑膜炎球菌fHBP序列的杂交多肽 |
EP2470205A1 (en) | 2009-08-27 | 2012-07-04 | Novartis AG | Adjuvant comprising aluminium, oligonucleotide and polycation |
JP5988492B2 (ja) | 2009-09-02 | 2016-09-07 | ノバルティス アーゲー | Tlr活性モジュレーターを含む免疫原性組成物 |
JO3257B1 (ar) | 2009-09-02 | 2018-09-16 | Novartis Ag | مركبات وتركيبات كمعدلات لفاعلية tlr |
RU2603267C2 (ru) | 2009-09-30 | 2016-11-27 | Новартис Аг | Конъюгация капсульных полисахаридов staphylococcus aureus типа 5 и типа 8 |
CA2776004A1 (en) | 2009-09-30 | 2011-04-07 | Novartis Ag | Expression of meningococcal fhbp polypeptides |
MX2012004850A (es) | 2009-10-27 | 2012-05-22 | Novartis Ag | Polipeptidos fhbp meningococicos modificados. |
HUE034251T2 (en) | 2009-10-30 | 2018-02-28 | Glaxosmithkline Biologicals Sa | Purification of type 5 and type 8 capsular saccharides from Staphylococcus aureus |
WO2011057148A1 (en) | 2009-11-05 | 2011-05-12 | Irm Llc | Compounds and compositions as tlr-7 activity modulators |
BR112012014624A8 (pt) | 2009-12-15 | 2017-12-26 | Novartis Ag | suspensão homogênea de compostos de imunopotenciação e usos dos destes |
WO2012020326A1 (en) | 2010-03-18 | 2012-02-16 | Novartis Ag | Adjuvanted vaccines for serogroup b meningococcus |
JP5848748B2 (ja) | 2010-03-23 | 2016-01-27 | アイアールエム・リミテッド・ライアビリティ・カンパニーIrm,Llc | 感染症、炎症、呼吸器疾患などの処置に使用するtlr2アゴニストとしての化合物(システインベースのリポペプチド)および組成物 |
US9827300B2 (en) * | 2010-03-30 | 2017-11-28 | Children's Hospital & Research Center Oakland | Factor H binding proteins (FHBP) with altered properties and methods of use thereof |
WO2011149564A1 (en) | 2010-05-28 | 2011-12-01 | Tetris Online, Inc. | Interactive hybrid asynchronous computer game infrastructure |
CA2803239A1 (en) | 2010-06-25 | 2011-12-29 | Novartis Ag | Combinations of meningococcal factor h binding proteins |
PL2608805T3 (pl) | 2010-08-23 | 2017-12-29 | Wyeth Llc | Trwałe preparaty antygenów rLP2086 Neisseria meningitidis |
US9259462B2 (en) | 2010-09-10 | 2016-02-16 | Glaxosmithkline Biologicals Sa | Developments in meningococcal outer membrane vesicles |
CN103096920B (zh) | 2010-09-10 | 2016-03-23 | 惠氏有限责任公司 | 脑膜炎奈瑟球菌orf2086抗原的非脂质化变体 |
GB201101665D0 (en) | 2011-01-31 | 2011-03-16 | Novartis Ag | Immunogenic compositions |
CA2860331A1 (en) | 2010-12-24 | 2012-06-28 | Novartis Ag | Compounds |
CN107837394A (zh) | 2011-06-24 | 2018-03-27 | 埃皮托吉尼西斯有限公司 | 作为抗原特异性免疫调节剂的包含选择的载体、维生素、单宁和类黄酮的组合的药物组合物 |
EP2776069A1 (en) | 2011-11-07 | 2014-09-17 | Novartis AG | Carrier molecule comprising a spr0096 and a spr2021 antigen |
MY198910A (en) | 2012-03-09 | 2023-10-02 | Pfizer | Neisseria meningitidis compositions and methods thereof |
SA115360586B1 (ar) | 2012-03-09 | 2017-04-12 | فايزر انك | تركيبات لعلاج الالتهاب السحائي البكتيري وطرق لتحضيرها |
MX357538B (es) | 2012-06-14 | 2018-07-13 | Novartis Ag | Vacunas para meningococo de serogrupo x. |
CA2875391A1 (en) | 2012-07-27 | 2014-01-30 | Institut National De La Sante Et De La Recherche Medicale | Cd147 as receptor for pilus-mediated adhesion of meningococci to vascular endothelia |
JP6266631B2 (ja) | 2012-10-03 | 2018-01-24 | グラクソスミスクライン バイオロジカルズ ソシエテ アノニム | 免疫原性組成物 |
CA2900454A1 (en) * | 2013-02-07 | 2014-08-14 | Glaxosmithkline Biologicals Sa | Pharmaceutical compositions comprising vesicles |
WO2014136064A2 (en) | 2013-03-08 | 2014-09-12 | Pfizer Inc. | Immunogenic fusion polypeptides |
WO2015017817A1 (en) | 2013-08-02 | 2015-02-05 | Children's Hospital & Research Center Oakland | Non-naturally occurring factor h binding proteins (fhbp) and methods of use thereof |
KR102199096B1 (ko) | 2013-09-08 | 2021-01-06 | 화이자 인코포레이티드 | 나이세리아 메닌지티디스 조성물 및 그의 방법 |
ES2841378T3 (es) | 2014-02-28 | 2021-07-08 | Glaxosmithkline Biologicals Sa | Polipéptidos fHbp meningocócicos modificados |
RU2563804C1 (ru) * | 2014-05-30 | 2015-09-20 | Общество с ограниченной ответственностью "НекстГен" | Способ доставки нуклеиновых кислот в эукариотические клетки |
CA2954745A1 (en) | 2014-07-17 | 2016-01-21 | Glaxosmithkline Biologicals S.A. | Modified meningococcal fhbp polypeptides |
EA038940B1 (ru) * | 2014-07-17 | 2021-11-12 | Глаксосмитклайн Байолоджикалс С.А. | Менингококковые вакцины |
NZ729206A (en) | 2014-07-23 | 2022-07-01 | Children’S Hospital & Res Center At Oakland | Factor h binding protein variants and methods of use thereof |
EP3270959A1 (en) | 2015-02-19 | 2018-01-24 | Pfizer Inc | Neisseria meningitidis compositions and methods thereof |
WO2017175082A1 (en) | 2016-04-05 | 2017-10-12 | Gsk Vaccines S.R.L. | Immunogenic compositions |
EP3577130A2 (en) | 2017-01-31 | 2019-12-11 | Pfizer Inc | Neisseria meningitidis compositions and methods thereof |
BR112020001255A2 (pt) | 2017-07-21 | 2020-07-28 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | composições imunogênicas de neisseria meningitidis |
AU2018375133A1 (en) * | 2017-11-28 | 2020-06-18 | The Research Foundation Of The State University Of New York | Combined therapy and prophylaxis for genital tract infections |
EP3607967A1 (en) | 2018-08-09 | 2020-02-12 | GlaxoSmithKline Biologicals S.A. | Modified meningococcal fhbp polypeptides |
AU2021364838A1 (en) * | 2020-10-23 | 2023-06-08 | Omvax, Inc. | Compositions and methods for vaccination against neisseria gonorrhoeae |
GB202115151D0 (en) | 2021-10-21 | 2021-12-08 | Glaxosmithkline Biologicals Sa | Methods |
Family Cites Families (177)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2386796A (en) | 1942-08-05 | 1945-10-16 | Bond Crown & Cork Co | Extruding device |
DE2848965A1 (de) | 1978-11-11 | 1980-05-22 | Behringwerke Ag | Verfahren zur herstellung von membranproteinen aus neisseria meningitidis und diese enthaltende vaccine |
DE2855719A1 (de) | 1978-12-22 | 1980-07-10 | Siemens Ag | Zahnaerztliche handstueckanordnung |
US4336336A (en) | 1979-01-12 | 1982-06-22 | President And Fellows Of Harvard College | Fused gene and method of making and using same |
AU545912B2 (en) | 1980-03-10 | 1985-08-08 | Cetus Corporation | Cloned heterologous jive products in bacillies |
ZA811368B (en) | 1980-03-24 | 1982-04-28 | Genentech Inc | Bacterial polypedtide expression employing tryptophan promoter-operator |
NZ199722A (en) | 1981-02-25 | 1985-12-13 | Genentech Inc | Dna transfer vector for expression of exogenous polypeptide in yeast;transformed yeast strain |
PT74811B (en) | 1981-04-29 | 1983-10-26 | Biogen Nv | Bacillus cloning vectors recombinant dna molecules bacillus hosts transformed with them and methods for expressing foreign dna sequences and producing polypeptides coded thereby |
US4551433A (en) | 1981-05-18 | 1985-11-05 | Genentech, Inc. | Microbial hybrid promoters |
US4405712A (en) | 1981-07-01 | 1983-09-20 | The United States Of America As Represented By The Department Of Health And Human Services | LTR-Vectors |
US4603112A (en) | 1981-12-24 | 1986-07-29 | Health Research, Incorporated | Modified vaccinia virus |
US4769330A (en) | 1981-12-24 | 1988-09-06 | Health Research, Incorporated | Modified vaccinia virus and methods for making and using the same |
US4876197A (en) | 1983-02-22 | 1989-10-24 | Chiron Corporation | Eukaryotic regulatable transcription |
CA1341302C (en) | 1983-02-22 | 2001-10-09 | Rae Lyn Burke | Yeast expression systems with vectors having gapdh or pyk promoters and synthesis of foreign protein |
JPS59166086A (ja) | 1983-03-09 | 1984-09-19 | Teruhiko Beppu | 新規な発現型プラスミドとそれらを用いて仔牛プロキモシン遺伝子を大腸菌内で発現させる方法 |
US4546083A (en) | 1983-04-22 | 1985-10-08 | Stolle Research & Development Corporation | Method and device for cell culture growth |
US4588684A (en) | 1983-04-26 | 1986-05-13 | Chiron Corporation | a-Factor and its processing signals |
JPS59205983A (ja) | 1983-04-28 | 1984-11-21 | ジエネツクス・コ−ポレイシヨン | 異種遺伝子を原核微生物で発現させる方法 |
US4663280A (en) | 1983-05-19 | 1987-05-05 | Public Health Research Institute Of The City Of New York | Expression and secretion vectors and method of constructing vectors |
IE58011B1 (en) | 1983-05-27 | 1993-06-16 | Texas A & M Univ Sys | Method for producing a recombinant baculovirus expression vector |
US4689406A (en) | 1983-08-10 | 1987-08-25 | Amgen | Enhancement of microbial expression of polypeptides |
US4870008A (en) | 1983-08-12 | 1989-09-26 | Chiron Corporation | Secretory expression in eukaryotes |
JPS6054685A (ja) | 1983-09-02 | 1985-03-29 | Suntory Ltd | 改良発現ベクタ−およびその利用 |
EP0136907A3 (en) | 1983-10-03 | 1986-12-30 | Genentech, Inc. | A xenogeneic expression control system, a method of using it, expression vectors containing it, cells transformed thereby and heterologous proteins produced therefrom |
ZA848495B (en) | 1984-01-31 | 1985-09-25 | Idaho Res Found | Production of polypeptides in insect cells |
DE3587759T2 (de) | 1984-05-11 | 1994-07-07 | Chiron Corp | Erhöhte Hefetranskription unter Verwendung einer Hybridkonstruktion der Promotorregion. |
US4880734A (en) | 1984-05-11 | 1989-11-14 | Chiron Corporation | Eukaryotic regulatable transcription |
CA1282721C (en) | 1984-06-04 | 1991-04-09 | Bernard Roizman | Herpes simplex virus as a vector |
US5288641A (en) | 1984-06-04 | 1994-02-22 | Arch Development Corporation | Herpes Simplex virus as a vector |
US4738921A (en) | 1984-09-27 | 1988-04-19 | Eli Lilly And Company | Derivative of the tryptophan operon for expression of fused gene products |
US4745056A (en) | 1984-10-23 | 1988-05-17 | Biotechnica International, Inc. | Streptomyces secretion vector |
US4837148A (en) | 1984-10-30 | 1989-06-06 | Phillips Petroleum Company | Autonomous replication sequences for yeast strains of the genus pichia |
US4762915A (en) | 1985-01-18 | 1988-08-09 | Liposome Technology, Inc. | Protein-liposome conjugates |
US4797368A (en) | 1985-03-15 | 1989-01-10 | The United States Of America As Represented By The Department Of Health And Human Services | Adeno-associated virus as eukaryotic expression vector |
ATE63757T1 (de) | 1985-03-28 | 1991-06-15 | Chiron Corp | Expression durch verwendung von fusionsgenen fuer proteinproduktion. |
US4865974A (en) | 1985-09-20 | 1989-09-12 | Cetus Corporation | Bacterial methionine N-terminal peptidase |
US4777127A (en) | 1985-09-30 | 1988-10-11 | Labsystems Oy | Human retrovirus-related products and methods of diagnosing and treating conditions associated with said retrovirus |
JPS6296086A (ja) | 1985-10-21 | 1987-05-02 | Agency Of Ind Science & Technol | 複合プラスミド |
US5139941A (en) | 1985-10-31 | 1992-08-18 | University Of Florida Research Foundation, Inc. | AAV transduction vectors |
US5091309A (en) | 1986-01-16 | 1992-02-25 | Washington University | Sindbis virus vectors |
US4861719A (en) | 1986-04-25 | 1989-08-29 | Fred Hutchinson Cancer Research Center | DNA constructs for retrovirus packaging cell lines |
EP0244042B1 (en) | 1986-05-02 | 1994-08-17 | Gist-Brocades N.V. | Secretory signal selection vectors for extracellular protein synthesis in bacilli |
JP2612874B2 (ja) | 1986-10-02 | 1997-05-21 | マサチユセツツ・インスチチユート・オブ・テクノロジー | タンパク質の代謝的安定性を調節する方法 |
JPS63123383A (ja) | 1986-11-11 | 1988-05-27 | Mitsubishi Kasei Corp | ハイブリツドプロモ−タ−、発現調節dna配列および発現ベクタ− |
GB8702816D0 (en) | 1987-02-07 | 1987-03-11 | Al Sumidaie A M K | Obtaining retrovirus-containing fraction |
US5219740A (en) | 1987-02-13 | 1993-06-15 | Fred Hutchinson Cancer Research Center | Retroviral gene transfer into diploid fibroblasts for gene therapy |
JP2795850B2 (ja) | 1987-03-23 | 1998-09-10 | ザイモジェネティクス,インコーポレイティド | 酵母発現ベクター |
US4980289A (en) | 1987-04-27 | 1990-12-25 | Wisconsin Alumni Research Foundation | Promoter deficient retroviral vector |
WO1989001973A2 (en) | 1987-09-02 | 1989-03-09 | Applied Biotechnology, Inc. | Recombinant pox virus for immunization against tumor-associated antigens |
DK463887D0 (da) | 1987-09-07 | 1987-09-07 | Novo Industri As | Gaerleader |
EP0378576B1 (en) | 1987-09-11 | 1995-01-18 | Whitehead Institute For Biomedical Research | Transduced fibroblasts and uses therefor |
US4929555A (en) | 1987-10-19 | 1990-05-29 | Phillips Petroleum Company | Pichia transformation |
CN1049686C (zh) | 1987-11-18 | 2000-02-23 | 希龙股份有限公司 | 非a和非b肝炎病毒的诊断及疫苗 |
SE456639B (sv) | 1987-11-27 | 1988-10-24 | Golf Comback Ab C O Wiklund | Golftraeningsanordning innefattande ett hus med lintrumma |
WO1989005349A1 (en) | 1987-12-09 | 1989-06-15 | The Australian National University | Method of combating viral infections |
CA1340772C (en) | 1987-12-30 | 1999-09-28 | Patricia Tekamp-Olson | Expression and secretion of heterologous protiens in yeast employing truncated alpha-factor leader sequences |
US4973551A (en) | 1988-01-15 | 1990-11-27 | Merck & Co., Inc. | Vector for the expression of fusion proteins and protein immunogens |
US5662896A (en) | 1988-03-21 | 1997-09-02 | Chiron Viagene, Inc. | Compositions and methods for cancer immunotherapy |
CN1038306A (zh) | 1988-03-21 | 1989-12-27 | 维吉恩公司 | 重组反转录病毒 |
US5591624A (en) | 1988-03-21 | 1997-01-07 | Chiron Viagene, Inc. | Retroviral packaging cell lines |
US5206152A (en) | 1988-04-08 | 1993-04-27 | Arch Development Corporation | Cloning and expression of early growth regulatory protein genes |
US5422120A (en) | 1988-05-30 | 1995-06-06 | Depotech Corporation | Heterovesicular liposomes |
AP129A (en) | 1988-06-03 | 1991-04-17 | Smithkline Biologicals S A | Expression of retrovirus gag protein eukaryotic cells |
CA1339354C (en) | 1988-09-01 | 1997-08-26 | The Whitehead Institute For Biomedical Research | Recombinant retroviruses with amphotropic and ecotropic host ranges |
US7118757B1 (en) * | 1988-12-19 | 2006-10-10 | Wyeth Holdings Corporation | Meningococcal class 1 outer-membrane protein vaccine |
ES2070312T5 (es) * | 1988-12-19 | 2003-05-16 | American Cyanamid Co | Vacuna de proteina de membrana exterior meningococica de clase 1. |
US5217879A (en) | 1989-01-12 | 1993-06-08 | Washington University | Infectious Sindbis virus vectors |
EP0832980B1 (en) | 1989-01-23 | 2002-06-19 | Chiron Corporation | Recombinant therapies for infection and hyperproliferative disorders |
CA2045129A1 (en) | 1989-02-01 | 1990-08-02 | Alfred I. Geller | Herpes simplex virus type i expression vector |
JP3140757B2 (ja) | 1989-02-06 | 2001-03-05 | デイナ・フアーバー・キヤンサー・インステイテユート | パッケージング欠陥hivプロウイルス、細胞系及びその使用 |
KR920701453A (ko) | 1989-03-17 | 1992-08-11 | 미리엄 디. 멕코나헤이 | 유전자발현의 외부조절 |
JP3250802B2 (ja) | 1989-03-21 | 2002-01-28 | バイカル・インコーポレイテッド | 脊椎動物における外因性ポリヌクレオチド配列の発現 |
US5703055A (en) | 1989-03-21 | 1997-12-30 | Wisconsin Alumni Research Foundation | Generation of antibodies through lipid mediated DNA delivery |
CA2017507C (en) | 1989-05-25 | 1996-11-12 | Gary Van Nest | Adjuvant formulation comprising a submicron oil droplet emulsion |
CA2064718A1 (en) | 1989-08-15 | 1991-02-16 | Mark Ian Hoschke | Absorption of zinc vapour in molten lead |
AU648261B2 (en) | 1989-08-18 | 1994-04-21 | Novartis Vaccines And Diagnostics, Inc. | Recombinant retroviruses delivering vector constructs to target cells |
US5585362A (en) | 1989-08-22 | 1996-12-17 | The Regents Of The University Of Michigan | Adenovirus vectors for gene therapy |
US5166057A (en) | 1989-08-28 | 1992-11-24 | The Mount Sinai School Of Medicine Of The City University Of New York | Recombinant negative strand rna virus expression-systems |
GB8919607D0 (en) | 1989-08-30 | 1989-10-11 | Wellcome Found | Novel entities for cancer therapy |
AU7007491A (en) | 1990-02-02 | 1991-08-08 | Schweiz. Serum- & Impfinstitut Bern | Cdna corresponding to the genome of negative-strand rna viruses, and process for the production of infectious negative-strand rna viruses |
ZA911974B (en) | 1990-03-21 | 1994-08-22 | Res Dev Foundation | Heterovesicular liposomes |
CA2039921A1 (en) | 1990-04-16 | 1991-10-17 | Xandra O. Breakefield | Transfer and expression of gene sequences into central nervous system cells using herpes simplex virus mutants with deletions in genes for viral replication |
AU7906691A (en) | 1990-05-23 | 1991-12-10 | United States of America, as represented by the Secretary, U.S. Department of Commerce, The | Adeno-associated virus (aav)-based eucaryotic vectors |
US5149655A (en) | 1990-06-21 | 1992-09-22 | Agracetus, Inc. | Apparatus for genetic transformation |
IE912559A1 (en) | 1990-07-19 | 1992-01-29 | Merck & Co Inc | The class ii protein of the outer membrane of neisseria¹meningitidis, and vaccines containing same |
AU665176B2 (en) | 1990-09-21 | 1995-12-21 | Novartis Vaccines And Diagnostics, Inc. | Packaging cells |
US5173414A (en) | 1990-10-30 | 1992-12-22 | Applied Immune Sciences, Inc. | Production of recombinant adeno-associated virus vectors |
WO1992007945A1 (en) | 1990-10-30 | 1992-05-14 | Dana Farber Cancer Institute | Cell type specific alteration of levels of gene products in neural cells |
SE9003978D0 (sv) | 1990-12-13 | 1990-12-13 | Henrik Garoff | Dna expressionssystem baserade paa ett virus replikon |
CA2098849C (en) | 1990-12-20 | 2007-07-10 | Ralph R. Weichselbaum | Control of gene expression by ionizing radiation |
WO1993003769A1 (en) | 1991-08-20 | 1993-03-04 | THE UNITED STATES OF AMERICA, represented by THE SECRETARY, DEPARTEMENT OF HEALTH AND HUMAN SERVICES | Adenovirus mediated transfer of genes to the gastrointestinal tract |
FR2681786A1 (fr) | 1991-09-27 | 1993-04-02 | Centre Nat Rech Scient | Vecteurs recombinants d'origine virale, leur procede d'obtention et leur utilisation pour l'expression de polypeptides dans des cellules musculaires. |
IL103059A0 (en) | 1991-09-30 | 1993-02-21 | Boehringer Ingelheim Int | Conjugates for introducing nucleic acid into higher eucaryotic cells |
NZ244306A (en) | 1991-09-30 | 1995-07-26 | Boehringer Ingelheim Int | Composition for introducing nucleic acid complexes into eucaryotic cells, complex containing nucleic acid and endosomolytic agent, peptide with endosomolytic domain and nucleic acid binding domain and preparation |
US5252479A (en) | 1991-11-08 | 1993-10-12 | Research Corporation Technologies, Inc. | Safe vector for gene therapy |
WO1993010218A1 (en) | 1991-11-14 | 1993-05-27 | The United States Government As Represented By The Secretary Of The Department Of Health And Human Services | Vectors including foreign genes and negative selective markers |
GB9125623D0 (en) | 1991-12-02 | 1992-01-29 | Dynal As | Cell modification |
EP0625049A4 (en) | 1992-01-23 | 1995-07-12 | Vical Inc | EX VIVO GENTRANSFER. |
DE69334197T2 (de) | 1992-03-02 | 2008-12-11 | Novartis Vaccines And Diagnostics S.R.L. | Helicobacter pylori Cytotoxin verwendbar in Impfstoffe und Diagnostik |
FR2688514A1 (fr) | 1992-03-16 | 1993-09-17 | Centre Nat Rech Scient | Adenovirus recombinants defectifs exprimant des cytokines et medicaments antitumoraux les contenant. |
WO1993025234A1 (en) | 1992-06-08 | 1993-12-23 | The Regents Of The University Of California | Methods and compositions for targeting specific tissue |
CA2137361A1 (en) | 1992-06-10 | 1993-12-23 | W. French Anderson | Vector particles resistant to inactivation by human serum |
GB2269175A (en) | 1992-07-31 | 1994-02-02 | Imperial College | Retroviral vectors |
HU219304B (en) | 1992-09-25 | 2001-03-28 | Inst Nat Sante Rech Med | Recombinant adenovirus derived vectors for the transfer of foreign genes into cells of the central nervous system, pharmaceutical preparations containing them and processes for their production |
EP1321526A3 (en) | 1992-11-18 | 2003-07-02 | Arch Development Corporation | Adenovirus-mediated gene transfer to cardiac and vascular smooth muscle |
WO1994012369A1 (en) | 1992-12-02 | 1994-06-09 | Corinna Morini | Optical signalling device for vehicles and water-borne craft |
WO1994012649A2 (en) | 1992-12-03 | 1994-06-09 | Genzyme Corporation | Gene therapy for cystic fibrosis |
US5478745A (en) | 1992-12-04 | 1995-12-26 | University Of Pittsburgh | Recombinant viral vector system |
US5348358A (en) | 1993-02-22 | 1994-09-20 | Selick David A | Contact lens insertion tool |
DE4311651A1 (de) | 1993-04-08 | 1994-10-13 | Boehringer Ingelheim Int | Virus für den Transport von Fremd-DNA in höhere eukaryotische Zellen |
AU6818094A (en) | 1993-04-22 | 1994-11-08 | Depotech Corporation | Cyclodextrin liposomes encapsulating pharmacologic compounds and methods for their use |
EP0624376B1 (en) * | 1993-05-13 | 2000-03-15 | American Cyanamid Company | Preparation and uses of LOS-depleted outer membrane proteins of gram-negative cocci |
CA2162271A1 (en) | 1993-05-26 | 1994-12-08 | Robert Kotin | Fusion proteins containing adeno-associated virus rep protein and bacterial protein |
FR2705686B1 (fr) | 1993-05-28 | 1995-08-18 | Transgene Sa | Nouveaux adénovirus défectifs et lignées de complémentation correspondantes. |
WO1995000655A1 (en) | 1993-06-24 | 1995-01-05 | Mc Master University | Adenovirus vectors for gene therapy |
BR9405507A (pt) | 1993-07-13 | 1999-05-25 | Rhone Poulenc Rorer Sa | Adenovirus recombinante defeituoso linhagem celular e composição farmaceutica |
US5439808A (en) | 1993-07-23 | 1995-08-08 | North American Vaccine, Inc. | Method for the high level expression, purification and refolding of the outer membrane group B porin proteins from Neisseria meningitidis |
WO1995004139A1 (en) | 1993-07-27 | 1995-02-09 | The Wistar Institute Of Anatomy And Biology | Modified dna virus vectors and uses therefor |
US5631236A (en) | 1993-08-26 | 1997-05-20 | Baylor College Of Medicine | Gene therapy for solid tumors, using a DNA sequence encoding HSV-Tk or VZV-Tk |
US5362865A (en) | 1993-09-02 | 1994-11-08 | Monsanto Company | Enhanced expression in plants using non-translated leader sequences |
ATE257176T1 (de) | 1993-09-15 | 2004-01-15 | Chiron Corp | Rekombinanter alphavirus vektor |
FR2710536B1 (fr) | 1993-09-29 | 1995-12-22 | Transgene Sa | Usage anti-cancéreux d'un vecteur viral comportant un gène modulateur de la réponse immunitaire et/ou inflammatoire. |
EP0723460A4 (en) | 1993-10-01 | 1998-09-30 | Us Health | GENE THERAPY FOR THE NERVOUS SYSTEM |
EP1637608B1 (en) | 1993-10-25 | 2009-07-22 | CANJI, Inc. | Recombinant adenoviral vector and methods of use |
ATE196248T1 (de) | 1993-11-16 | 2000-09-15 | Skyepharma Inc | Vesikel mit gesteuerter wirkstofffreisetzung |
US5693506A (en) | 1993-11-16 | 1997-12-02 | The Regents Of The University Of California | Process for protein production in plants |
FR2712603B1 (fr) | 1993-11-18 | 1996-02-09 | Centre Nat Rech Scient | Virus recombinants, préparation et utilisation en thérapie génique. |
JPH07241786A (ja) | 1994-03-08 | 1995-09-19 | Fanuc Ltd | 産業用ロボットの制御装置 |
US6780406B1 (en) | 1994-03-21 | 2004-08-24 | The Regents Of The University Of Michigan | Inhibition of vascular smooth muscle cell proliferation administering a thymidine kinase gene |
US7252989B1 (en) | 1994-04-04 | 2007-08-07 | Board Of Regents, The University Of Texas System | Adenovirus supervector system |
ATE173634T1 (de) | 1994-04-20 | 1998-12-15 | Us Army | Impfstoff gegen gram-negative bakterielle infektionen |
EP0763103A4 (en) | 1994-04-28 | 1998-07-15 | Univ Michigan | GENE DELIVERY VECTOR USING PLASMID DNA ENCAPSULATED IN ADENOVIRUS AND CELL LINE OF ENCAPSIDATION |
ES2297831T3 (es) | 1994-05-09 | 2008-05-01 | Oxford Biomedica (Uk) Limited | Vectores retroviricos que presentan una tasa de recombinacion reducida. |
EP1548118A2 (en) | 1994-06-10 | 2005-06-29 | Genvec, Inc. | Complementary adenoviral vector systems and cell lines |
FR2723588B1 (fr) | 1994-08-12 | 1996-09-20 | Rhone Poulenc Rorer Sa | Adenovirus comprenant un gene codant pour la glutathion peroxydase |
IL117483A (en) | 1995-03-17 | 2008-03-20 | Bernard Brodeur | MENINGITIDIS NEISSERIA shell protein is resistant to proteinase K. |
US6180111B1 (en) | 1995-05-18 | 2001-01-30 | University Of Maryland | Vaccine delivery system |
JPH11505128A (ja) | 1995-05-22 | 1999-05-18 | カイロン コーポレイション | キメラインテグラーゼタンパク質に媒介される真核生物ゲノム中へのベクター構築物の位置特異的組み込み |
WO1997028273A1 (en) | 1996-02-01 | 1997-08-07 | North American Vaccine, Inc. | Expression of group b neisseria meningitidis outer membrane (mb3) protein from yeast and vaccines |
US5753235A (en) | 1996-02-15 | 1998-05-19 | Heska Corporation | Recombinant canine herpesviruses |
DE19630390A1 (de) | 1996-07-26 | 1998-01-29 | Chiron Behring Gmbh & Co | Proteine, insbesondere Membranproteine von Helicobacter pylori, ihre Herstellung und Verwendung |
CA2264012C (en) | 1996-08-13 | 2011-04-26 | Chiron Corporation | Compositions and methods for polynucleotide delivery |
CA2264585C (en) * | 1996-08-27 | 2005-06-14 | Chiron Corporation | Monoclonal antibodies that define unique meningococcal b epitopes and their use in the preparation of vaccine compositions |
GB9619185D0 (en) | 1996-09-13 | 1996-10-23 | Pest West Electronics Ltd | Insect catching device |
AU5426098A (en) | 1996-10-24 | 1998-05-15 | Emory University | Invasion associated genes from (neisseria meningitidis) serogroup |
US5980898A (en) | 1996-11-14 | 1999-11-09 | The United States Of America As Represented By The U.S. Army Medical Research & Material Command | Adjuvant for transcutaneous immunization |
US6451317B1 (en) | 1997-07-17 | 2002-09-17 | Baxter International Inc. | Immunogenic conjugates comprising a Group B meningococcal porin and an H influenzae polysaccharide |
DE69841807D1 (de) | 1997-11-06 | 2010-09-16 | Novartis Vaccines & Diagnostic | Neisseriale antigene |
CA2311810A1 (en) | 1997-11-28 | 1999-06-10 | Steven Ray | Molten metal filtration |
GB9726398D0 (en) * | 1997-12-12 | 1998-02-11 | Isis Innovation | Polypeptide and coding sequences |
AU1979599A (en) * | 1998-01-14 | 1999-08-02 | Chiron S.P.A. | (neisseria meningitidis) antigens |
GB9807721D0 (en) | 1998-04-08 | 1998-06-10 | Chiron Spa | Antigen |
GB9808866D0 (en) | 1998-04-24 | 1998-06-24 | Smithkline Beecham Biolog | Novel compounds |
US20070026021A1 (en) * | 1998-05-01 | 2007-02-01 | Chiron S.R.I. | Neisseria meningitidis antigens and compositions |
EP1093517B1 (en) | 1998-05-01 | 2008-03-05 | Novartis Vaccines and Diagnostics, Inc. | Neisseria meningitidis antigens and compositions |
GB9810276D0 (en) | 1998-05-13 | 1998-07-15 | Smithkline Beecham Biolog | Novel compounds |
PT1079857E (pt) * | 1998-05-29 | 2007-02-28 | Statens Inst For Folkehelse | Combinação de vacinas para a meningite b e c |
CA2346713A1 (en) | 1998-10-09 | 2000-04-20 | Chiron Corporation | Neisseria genomic sequences and methods of their use |
GB9823978D0 (en) | 1998-11-02 | 1998-12-30 | Microbiological Res Authority | Multicomponent meningococcal vaccine |
NZ581940A (en) | 1999-04-30 | 2011-07-29 | Novartis Vaccines & Diagnostic | Conserved neisserial antigens |
CA2371032A1 (en) | 1999-04-30 | 2000-11-09 | Chiron Corporation | Neisseria genomic sequences and methods of their use |
PT2275553E (pt) | 1999-10-29 | 2015-09-18 | Glaxosmithkline Biolog Sa | Péptidos antigénicos de neisseria |
WO2001034642A2 (en) | 1999-11-12 | 2001-05-17 | University Of Iowa Research Foundation | Control of neisserial membrane synthesis |
BR0107679A (pt) * | 2000-01-17 | 2004-07-06 | Chiron Spa | Vacina de vesìcula de membrana externa (omv) compreendendo proteìnas de membrana externa do grupo sérico b de neisseria meningitidis |
WO2001064922A2 (en) | 2000-02-28 | 2001-09-07 | Chiron Spa | Heterologous expression of neisserial proteins |
BRPI0112928B1 (pt) | 2000-07-27 | 2017-08-29 | Children's Hospital & Research Center At Oakland | A composition comprising preparations comprising outer membrane vesicles (OMV), microvesicles (MV) or both MVO and MV |
GB0121591D0 (en) | 2001-09-06 | 2001-10-24 | Chiron Spa | Hybrid and tandem expression of neisserial proteins |
MX339524B (es) | 2001-10-11 | 2016-05-30 | Wyeth Corp | Composiciones inmunogenicas novedosas para la prevencion y tratamiento de enfermedad meningococica. |
US7785608B2 (en) * | 2002-08-30 | 2010-08-31 | Wyeth Holdings Corporation | Immunogenic compositions for the prevention and treatment of meningococcal disease |
GB0220194D0 (en) | 2002-08-30 | 2002-10-09 | Chiron Spa | Improved vesicles |
CA2501812C (en) | 2002-10-11 | 2012-07-10 | Mariagrazia Pizza | Polypeptide-vaccines for broad protection against hypervirulent meningococcal lineages |
GB0227346D0 (en) | 2002-11-22 | 2002-12-31 | Chiron Spa | 741 |
CA2514328C (en) | 2003-01-30 | 2020-01-14 | Chiron Srl | Injectable vaccines against multiple meningococcal serogroups |
GB0316560D0 (en) | 2003-07-15 | 2003-08-20 | Chiron Srl | Vesicle filtration |
CA2540896C (en) | 2003-10-02 | 2015-06-02 | Chiron Srl | Liquid vaccines for multiple meningococcal serogroups |
GB0419408D0 (en) | 2004-09-01 | 2004-10-06 | Chiron Srl | 741 chimeric polypeptides |
NZ555937A (en) | 2005-01-27 | 2009-05-31 | Childrens Hosp & Res Ct Oak | GNA1870-based vesicle vaccines for broad spectrum protection against diseases caused by Neisseria meningitidis |
-
2001
- 2001-01-17 BR BR0107679-5A patent/BR0107679A/pt not_active IP Right Cessation
- 2001-01-17 EP EP10178595.4A patent/EP2289545B1/en not_active Expired - Lifetime
- 2001-01-17 AT AT01942562T patent/ATE476988T1/de active
- 2001-01-17 JP JP2001552932A patent/JP2003520248A/ja not_active Withdrawn
- 2001-01-17 CA CA2871789A patent/CA2871789C/en not_active Expired - Lifetime
- 2001-01-17 US US10/181,600 patent/US8273360B2/en active Active
- 2001-01-17 AU AU28754/01A patent/AU784518B2/en not_active Ceased
- 2001-01-17 DK DK10178595.4T patent/DK2289545T3/en active
- 2001-01-17 CN CN201110099744XA patent/CN102172398A/zh active Pending
- 2001-01-17 CA CA2397508A patent/CA2397508C/en not_active Expired - Lifetime
- 2001-01-17 DK DK07013453.1T patent/DK1897555T3/da active
- 2001-01-17 ES ES07013453.1T patent/ES2507100T3/es not_active Expired - Lifetime
- 2001-01-17 PT PT101785954T patent/PT2289545T/pt unknown
- 2001-01-17 EP EP07013453.1A patent/EP1897555B1/en not_active Expired - Lifetime
- 2001-01-17 CN CN018059201A patent/CN1416352B/zh not_active Expired - Fee Related
- 2001-01-17 MX MXPA02006962A patent/MXPA02006962A/es active IP Right Grant
- 2001-01-17 EP EP10008222.1A patent/EP2275129A3/en not_active Ceased
- 2001-01-17 EP EP10179761A patent/EP2281570A3/en not_active Withdrawn
- 2001-01-17 EP EP10179793A patent/EP2281571A3/en not_active Withdrawn
- 2001-01-17 DK DK01942562.8T patent/DK1248647T3/da active
- 2001-01-17 PT PT70134531T patent/PT1897555E/pt unknown
- 2001-01-17 BR BRPI0107679A patent/BRPI0107679B8/pt unknown
- 2001-01-17 WO PCT/IB2001/000166 patent/WO2001052885A1/en active IP Right Grant
- 2001-01-17 DE DE60142772T patent/DE60142772D1/de not_active Expired - Lifetime
- 2001-01-17 RU RU2002122111/15A patent/RU2279889C2/ru not_active IP Right Cessation
- 2001-01-17 PT PT01942562T patent/PT1248647E/pt unknown
- 2001-01-17 EP EP01942562A patent/EP1248647B1/en not_active Expired - Lifetime
- 2001-01-17 ES ES10178595.4T patent/ES2588917T3/es not_active Expired - Lifetime
- 2001-01-17 NZ NZ520466A patent/NZ520466A/en not_active IP Right Cessation
-
2009
- 2009-02-19 AU AU2009200692A patent/AU2009200692B2/en not_active Ceased
-
2010
- 2010-11-04 CY CY20101101003T patent/CY1111056T1/el unknown
-
2011
- 2011-03-18 JP JP2011061748A patent/JP2011116793A/ja active Pending
-
2012
- 2012-08-21 US US13/591,138 patent/US20120328643A1/en not_active Abandoned
-
2013
- 2013-06-13 JP JP2013124555A patent/JP2013181036A/ja active Pending
- 2013-06-13 JP JP2013124554A patent/JP5823446B2/ja not_active Expired - Fee Related
- 2013-06-13 JP JP2013124556A patent/JP2013181037A/ja active Pending
-
2014
- 2014-09-17 CY CY20141100751T patent/CY1115842T1/el unknown
-
2015
- 2015-07-23 JP JP2015145631A patent/JP2015193652A/ja active Pending
- 2015-10-13 US US14/882,320 patent/US20160030546A1/en not_active Abandoned
- 2015-12-07 US US14/961,725 patent/US20160082098A1/en not_active Abandoned
-
2016
- 2016-08-29 CY CY20161100845T patent/CY1117957T1/el unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5823446B2 (ja) | N.meningitidis血清型b外膜タンパク質を含む外膜小胞(omv)ワクチン | |
JP5102414B2 (ja) | 髄膜炎菌抗原および組成物 | |
JP2010187700A (ja) | 保存されたナイセリア抗原 | |
JP2013078340A (ja) | 抗原性髄膜炎菌性ペプチド | |
JP2011015684A (ja) | 抗原性ナイセリアペプチド | |
AU2006200732B2 (en) | Outer membrane vesicle (OMV) vaccine comprising N. meningitidis serogroup B outer membrane proteins | |
ES2348657T3 (es) | Vacuna de vesicula de membrana externa (omv) que comprende proteinas de membrana externa del serogrupo b de n. meningitidis. | |
RU2343159C2 (ru) | Антигены neisseria meningitidis |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20130613 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20140624 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20140905 |
|
A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20150331 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20150723 |
|
A911 | Transfer to examiner for re-examination before appeal (zenchi) |
Free format text: JAPANESE INTERMEDIATE CODE: A911 Effective date: 20150731 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20150911 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20151007 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 5823446 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313113 |
|
R371 | Transfer withdrawn |
Free format text: JAPANESE INTERMEDIATE CODE: R371 |
|
LAPS | Cancellation because of no payment of annual fees |