WO2013183786A1 - トランスポーターに対する抗体およびその用途 - Google Patents
トランスポーターに対する抗体およびその用途 Download PDFInfo
- Publication number
- WO2013183786A1 WO2013183786A1 PCT/JP2013/065996 JP2013065996W WO2013183786A1 WO 2013183786 A1 WO2013183786 A1 WO 2013183786A1 JP 2013065996 W JP2013065996 W JP 2013065996W WO 2013183786 A1 WO2013183786 A1 WO 2013183786A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- seq
- amino acid
- acid sequence
- antibody
- antigen
- Prior art date
Links
- 206010028980 Neoplasm Diseases 0.000 claims abstract description 40
- 101000605020 Homo sapiens Large neutral amino acids transporter small subunit 1 Proteins 0.000 claims abstract description 18
- 201000011510 cancer Diseases 0.000 claims abstract description 14
- 239000003814 drug Substances 0.000 claims abstract description 13
- 102100038204 Large neutral amino acids transporter small subunit 1 Human genes 0.000 claims abstract 24
- 101000800023 Homo sapiens 4F2 cell-surface antigen heavy chain Proteins 0.000 claims abstract 13
- 150000001413 amino acids Chemical class 0.000 claims description 158
- 210000004027 cell Anatomy 0.000 claims description 118
- 239000000427 antigen Substances 0.000 claims description 110
- 108091007433 antigens Proteins 0.000 claims description 110
- 102000036639 antigens Human genes 0.000 claims description 110
- 230000027455 binding Effects 0.000 claims description 108
- 239000012634 fragment Substances 0.000 claims description 100
- 108010047041 Complementarity Determining Regions Proteins 0.000 claims description 82
- 241000282414 Homo sapiens Species 0.000 claims description 49
- 230000000694 effects Effects 0.000 claims description 32
- 230000035772 mutation Effects 0.000 claims description 31
- 125000000539 amino acid group Chemical group 0.000 claims description 30
- 238000000034 method Methods 0.000 claims description 26
- 239000000203 mixture Substances 0.000 claims description 24
- 108090000623 proteins and genes Proteins 0.000 claims description 24
- 229940127121 immunoconjugate Drugs 0.000 claims description 22
- 210000004408 hybridoma Anatomy 0.000 claims description 20
- 206010009944 Colon cancer Diseases 0.000 claims description 14
- 108020004707 nucleic acids Proteins 0.000 claims description 13
- 102000039446 nucleic acids Human genes 0.000 claims description 13
- 150000007523 nucleic acids Chemical class 0.000 claims description 13
- 206010035226 Plasma cell myeloma Diseases 0.000 claims description 12
- 108091006232 SLC7A5 Proteins 0.000 claims description 12
- 239000013604 expression vector Substances 0.000 claims description 11
- 208000029742 colonic neoplasm Diseases 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 10
- 230000001472 cytotoxic effect Effects 0.000 claims description 9
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims description 8
- 201000005202 lung cancer Diseases 0.000 claims description 8
- 208000020816 lung neoplasm Diseases 0.000 claims description 8
- 239000012228 culture supernatant Substances 0.000 claims description 7
- 108010021625 Immunoglobulin Fragments Proteins 0.000 claims description 6
- 102000008394 Immunoglobulin Fragments Human genes 0.000 claims description 6
- 241000124008 Mammalia Species 0.000 claims description 6
- 230000006907 apoptotic process Effects 0.000 claims description 6
- 238000003384 imaging method Methods 0.000 claims description 6
- 206010005003 Bladder cancer Diseases 0.000 claims description 4
- 208000003174 Brain Neoplasms Diseases 0.000 claims description 4
- 206010006187 Breast cancer Diseases 0.000 claims description 4
- 208000026310 Breast neoplasm Diseases 0.000 claims description 4
- 208000001333 Colorectal Neoplasms Diseases 0.000 claims description 4
- 201000009273 Endometriosis Diseases 0.000 claims description 4
- 241000588724 Escherichia coli Species 0.000 claims description 4
- 206010025323 Lymphomas Diseases 0.000 claims description 4
- 206010061902 Pancreatic neoplasm Diseases 0.000 claims description 4
- 206010060862 Prostate cancer Diseases 0.000 claims description 4
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims description 4
- 208000005718 Stomach Neoplasms Diseases 0.000 claims description 4
- 208000007097 Urinary Bladder Neoplasms Diseases 0.000 claims description 4
- 208000006105 Uterine Cervical Neoplasms Diseases 0.000 claims description 4
- 239000002246 antineoplastic agent Substances 0.000 claims description 4
- 201000010881 cervical cancer Diseases 0.000 claims description 4
- 238000001514 detection method Methods 0.000 claims description 4
- 206010017758 gastric cancer Diseases 0.000 claims description 4
- 201000011066 hemangioma Diseases 0.000 claims description 4
- 201000007270 liver cancer Diseases 0.000 claims description 4
- 208000014018 liver neoplasm Diseases 0.000 claims description 4
- 208000015486 malignant pancreatic neoplasm Diseases 0.000 claims description 4
- 201000002528 pancreatic cancer Diseases 0.000 claims description 4
- 208000008443 pancreatic carcinoma Diseases 0.000 claims description 4
- 201000011549 stomach cancer Diseases 0.000 claims description 4
- 201000005112 urinary bladder cancer Diseases 0.000 claims description 4
- 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 claims description 3
- 206010008342 Cervix carcinoma Diseases 0.000 claims description 3
- 208000006332 Choriocarcinoma Diseases 0.000 claims description 3
- 206010014733 Endometrial cancer Diseases 0.000 claims description 3
- 206010014759 Endometrial neoplasm Diseases 0.000 claims description 3
- 208000000461 Esophageal Neoplasms Diseases 0.000 claims description 3
- 201000008808 Fibrosarcoma Diseases 0.000 claims description 3
- 208000022072 Gallbladder Neoplasms Diseases 0.000 claims description 3
- 208000032612 Glial tumor Diseases 0.000 claims description 3
- 206010018338 Glioma Diseases 0.000 claims description 3
- 208000007766 Kaposi sarcoma Diseases 0.000 claims description 3
- 206010023825 Laryngeal cancer Diseases 0.000 claims description 3
- 208000018142 Leiomyosarcoma Diseases 0.000 claims description 3
- 208000000172 Medulloblastoma Diseases 0.000 claims description 3
- 206010027406 Mesothelioma Diseases 0.000 claims description 3
- 208000003445 Mouth Neoplasms Diseases 0.000 claims description 3
- 208000034578 Multiple myelomas Diseases 0.000 claims description 3
- 206010029260 Neuroblastoma Diseases 0.000 claims description 3
- 201000004404 Neurofibroma Diseases 0.000 claims description 3
- 206010030155 Oesophageal carcinoma Diseases 0.000 claims description 3
- 206010033128 Ovarian cancer Diseases 0.000 claims description 3
- 206010061535 Ovarian neoplasm Diseases 0.000 claims description 3
- 208000009565 Pharyngeal Neoplasms Diseases 0.000 claims description 3
- 206010034811 Pharyngeal cancer Diseases 0.000 claims description 3
- 241000288906 Primates Species 0.000 claims description 3
- 208000006265 Renal cell carcinoma Diseases 0.000 claims description 3
- 208000000453 Skin Neoplasms Diseases 0.000 claims description 3
- 208000000102 Squamous Cell Carcinoma of Head and Neck Diseases 0.000 claims description 3
- 206010042971 T-cell lymphoma Diseases 0.000 claims description 3
- 208000027585 T-cell non-Hodgkin lymphoma Diseases 0.000 claims description 3
- 208000024770 Thyroid neoplasm Diseases 0.000 claims description 3
- 206010062129 Tongue neoplasm Diseases 0.000 claims description 3
- 208000006593 Urologic Neoplasms Diseases 0.000 claims description 3
- 208000008383 Wilms tumor Diseases 0.000 claims description 3
- 201000006828 endometrial hyperplasia Diseases 0.000 claims description 3
- 201000004101 esophageal cancer Diseases 0.000 claims description 3
- 201000010175 gallbladder cancer Diseases 0.000 claims description 3
- 208000005017 glioblastoma Diseases 0.000 claims description 3
- 201000000459 head and neck squamous cell carcinoma Diseases 0.000 claims description 3
- 201000002222 hemangioblastoma Diseases 0.000 claims description 3
- 206010023841 laryngeal neoplasm Diseases 0.000 claims description 3
- 208000032839 leukemia Diseases 0.000 claims description 3
- 208000012987 lip and oral cavity carcinoma Diseases 0.000 claims description 3
- 201000001441 melanoma Diseases 0.000 claims description 3
- 201000008026 nephroblastoma Diseases 0.000 claims description 3
- 201000008968 osteosarcoma Diseases 0.000 claims description 3
- 201000009410 rhabdomyosarcoma Diseases 0.000 claims description 3
- 230000028327 secretion Effects 0.000 claims description 3
- 201000000849 skin cancer Diseases 0.000 claims description 3
- 201000002510 thyroid cancer Diseases 0.000 claims description 3
- 201000009657 thyroid sarcoma Diseases 0.000 claims description 3
- 201000006134 tongue cancer Diseases 0.000 claims description 3
- 208000003163 Cavernous Hemangioma Diseases 0.000 claims description 2
- 241000238631 Hexapoda Species 0.000 claims description 2
- 201000000582 Retinoblastoma Diseases 0.000 claims description 2
- 239000002254 cytotoxic agent Substances 0.000 claims description 2
- 229940127089 cytotoxic agent Drugs 0.000 claims description 2
- 238000003745 diagnosis Methods 0.000 claims description 2
- 239000000539 dimer Substances 0.000 claims description 2
- 238000001727 in vivo Methods 0.000 claims description 2
- 210000004962 mammalian cell Anatomy 0.000 claims description 2
- 210000001161 mammalian embryo Anatomy 0.000 claims description 2
- 238000012360 testing method Methods 0.000 claims description 2
- 210000005253 yeast cell Anatomy 0.000 claims description 2
- 125000003275 alpha amino acid group Chemical group 0.000 claims 59
- 210000001130 astrocyte Anatomy 0.000 claims 1
- 210000004291 uterus Anatomy 0.000 claims 1
- 230000003013 cytotoxicity Effects 0.000 abstract description 7
- 231100000135 cytotoxicity Toxicity 0.000 abstract description 7
- 102000057630 human SLC7A5 Human genes 0.000 abstract description 5
- 239000004480 active ingredient Substances 0.000 abstract description 3
- 230000001419 dependent effect Effects 0.000 abstract description 3
- 230000000069 prophylactic effect Effects 0.000 abstract 1
- 229940124597 therapeutic agent Drugs 0.000 abstract 1
- 235000001014 amino acid Nutrition 0.000 description 29
- 229940024606 amino acid Drugs 0.000 description 29
- 239000002609 medium Substances 0.000 description 22
- 210000004881 tumor cell Anatomy 0.000 description 18
- 241000700159 Rattus Species 0.000 description 17
- 238000005406 washing Methods 0.000 description 16
- 235000018102 proteins Nutrition 0.000 description 13
- 102000004169 proteins and genes Human genes 0.000 description 13
- 108060003951 Immunoglobulin Proteins 0.000 description 11
- 241000699666 Mus <mouse, genus> Species 0.000 description 11
- 102000018358 immunoglobulin Human genes 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 9
- 201000000050 myeloid neoplasm Diseases 0.000 description 9
- 210000000628 antibody-producing cell Anatomy 0.000 description 8
- 230000004927 fusion Effects 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 8
- 230000032258 transport Effects 0.000 description 8
- 230000030833 cell death Effects 0.000 description 7
- 238000005259 measurement Methods 0.000 description 7
- 108020004414 DNA Proteins 0.000 description 6
- 241001465754 Metazoa Species 0.000 description 6
- 241000699670 Mus sp. Species 0.000 description 6
- 239000012636 effector Substances 0.000 description 6
- 210000000952 spleen Anatomy 0.000 description 6
- 239000006228 supernatant Substances 0.000 description 6
- 108090000790 Enzymes Proteins 0.000 description 5
- 102000004190 Enzymes Human genes 0.000 description 5
- 239000004698 Polyethylene Substances 0.000 description 5
- 230000000259 anti-tumor effect Effects 0.000 description 5
- 230000004071 biological effect Effects 0.000 description 5
- 210000004369 blood Anatomy 0.000 description 5
- 239000008280 blood Substances 0.000 description 5
- 210000000170 cell membrane Anatomy 0.000 description 5
- 239000006285 cell suspension Substances 0.000 description 5
- 239000002299 complementary DNA Substances 0.000 description 5
- 239000003145 cytotoxic factor Substances 0.000 description 5
- 239000008188 pellet Substances 0.000 description 5
- 239000008194 pharmaceutical composition Substances 0.000 description 5
- 108090000765 processed proteins & peptides Proteins 0.000 description 5
- 210000004989 spleen cell Anatomy 0.000 description 5
- 230000002269 spontaneous effect Effects 0.000 description 5
- 108010078791 Carrier Proteins Proteins 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 230000022534 cell killing Effects 0.000 description 4
- 238000005119 centrifugation Methods 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000006471 dimerization reaction Methods 0.000 description 4
- 230000003053 immunization Effects 0.000 description 4
- 238000002649 immunization Methods 0.000 description 4
- 238000003018 immunoassay Methods 0.000 description 4
- 229940072221 immunoglobulins Drugs 0.000 description 4
- 238000011534 incubation Methods 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 239000013612 plasmid Substances 0.000 description 4
- LPXQRXLUHJKZIE-UHFFFAOYSA-N 8-azaguanine Chemical compound NC1=NC(O)=C2NN=NC2=N1 LPXQRXLUHJKZIE-UHFFFAOYSA-N 0.000 description 3
- 229960005508 8-azaguanine Drugs 0.000 description 3
- 102000034263 Amino acid transporters Human genes 0.000 description 3
- 108050005273 Amino acid transporters Proteins 0.000 description 3
- 206010003445 Ascites Diseases 0.000 description 3
- 241000283690 Bos taurus Species 0.000 description 3
- 239000006144 Dulbecco’s modified Eagle's medium Substances 0.000 description 3
- 241000282412 Homo Species 0.000 description 3
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 description 3
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 description 3
- 239000012980 RPMI-1640 medium Substances 0.000 description 3
- 230000010056 antibody-dependent cellular cytotoxicity Effects 0.000 description 3
- 239000000872 buffer Substances 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 229940088598 enzyme Drugs 0.000 description 3
- ZDXPYRJPNDTMRX-UHFFFAOYSA-N glutamine Natural products OC(=O)C(N)CCC(N)=O ZDXPYRJPNDTMRX-UHFFFAOYSA-N 0.000 description 3
- 230000001939 inductive effect Effects 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 210000004988 splenocyte Anatomy 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 description 2
- 108091032973 (ribonucleotides)n+m Proteins 0.000 description 2
- OGNSCSPNOLGXSM-UHFFFAOYSA-N 2,4-diaminobutyric acid Chemical compound NCCC(N)C(O)=O OGNSCSPNOLGXSM-UHFFFAOYSA-N 0.000 description 2
- OYIFNHCXNCRBQI-UHFFFAOYSA-N 2-aminoadipic acid Chemical compound OC(=O)C(N)CCCC(O)=O OYIFNHCXNCRBQI-UHFFFAOYSA-N 0.000 description 2
- PECYZEOJVXMISF-UHFFFAOYSA-N 3-aminoalanine Chemical compound [NH3+]CC(N)C([O-])=O PECYZEOJVXMISF-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 102100033400 4F2 cell-surface antigen heavy chain Human genes 0.000 description 2
- 239000004475 Arginine Substances 0.000 description 2
- DCXYFEDJOCDNAF-UHFFFAOYSA-N Asparagine Natural products OC(=O)C(N)CC(N)=O DCXYFEDJOCDNAF-UHFFFAOYSA-N 0.000 description 2
- 206010003571 Astrocytoma Diseases 0.000 description 2
- 108091003079 Bovine Serum Albumin Proteins 0.000 description 2
- 241000282693 Cercopithecidae Species 0.000 description 2
- 108091026890 Coding region Proteins 0.000 description 2
- 238000002965 ELISA Methods 0.000 description 2
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- 108010054477 Immunoglobulin Fab Fragments Proteins 0.000 description 2
- 102000001706 Immunoglobulin Fab Fragments Human genes 0.000 description 2
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical group OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 description 2
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 2
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 description 2
- DCXYFEDJOCDNAF-REOHCLBHSA-N L-asparagine Chemical compound OC(=O)[C@@H](N)CC(N)=O DCXYFEDJOCDNAF-REOHCLBHSA-N 0.000 description 2
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 2
- ZDXPYRJPNDTMRX-VKHMYHEASA-N L-glutamine Chemical compound OC(=O)[C@@H](N)CCC(N)=O ZDXPYRJPNDTMRX-VKHMYHEASA-N 0.000 description 2
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 2
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 2
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 description 2
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 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
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 2
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 description 2
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 2
- 239000004472 Lysine Substances 0.000 description 2
- 102000018697 Membrane Proteins Human genes 0.000 description 2
- 108010052285 Membrane Proteins Proteins 0.000 description 2
- 108010036505 Neutral Amino Acid Transport Systems Proteins 0.000 description 2
- 102000012106 Neutral Amino Acid Transport Systems Human genes 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 229920002535 Polyethylene Glycol 1500 Polymers 0.000 description 2
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Chemical group OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 description 2
- 108091006313 SLC3A2 Proteins 0.000 description 2
- 101100462087 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) LAT1 gene Proteins 0.000 description 2
- 229920002684 Sepharose Polymers 0.000 description 2
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 2
- AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 description 2
- 239000004473 Threonine 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
- 101710120037 Toxin CcdB Proteins 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
- KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Natural products CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 235000004279 alanine Nutrition 0.000 description 2
- QWCKQJZIFLGMSD-UHFFFAOYSA-N alpha-aminobutyric acid Chemical compound CCC(N)C(O)=O QWCKQJZIFLGMSD-UHFFFAOYSA-N 0.000 description 2
- 229960003896 aminopterin Drugs 0.000 description 2
- 229940125644 antibody drug Drugs 0.000 description 2
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 2
- -1 aromatic amino acids Chemical class 0.000 description 2
- 235000009582 asparagine Nutrition 0.000 description 2
- 229960001230 asparagine Drugs 0.000 description 2
- 235000003704 aspartic acid Nutrition 0.000 description 2
- 239000007640 basal medium Substances 0.000 description 2
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 2
- 210000004899 c-terminal region Anatomy 0.000 description 2
- 210000005056 cell body Anatomy 0.000 description 2
- 230000007910 cell fusion Effects 0.000 description 2
- 210000003855 cell nucleus Anatomy 0.000 description 2
- 238000012412 chemical coupling Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000012258 culturing Methods 0.000 description 2
- 235000018417 cysteine Nutrition 0.000 description 2
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 2
- 125000000151 cysteine group Chemical group N[C@@H](CS)C(=O)* 0.000 description 2
- 231100000433 cytotoxic Toxicity 0.000 description 2
- PMMYEEVYMWASQN-UHFFFAOYSA-N dl-hydroxyproline Natural products OC1C[NH2+]C(C([O-])=O)C1 PMMYEEVYMWASQN-UHFFFAOYSA-N 0.000 description 2
- 239000002552 dosage form Substances 0.000 description 2
- 210000003743 erythrocyte Anatomy 0.000 description 2
- 239000012894 fetal calf serum Substances 0.000 description 2
- 238000001943 fluorescence-activated cell sorting Methods 0.000 description 2
- 235000013922 glutamic acid Nutrition 0.000 description 2
- 239000004220 glutamic acid Substances 0.000 description 2
- FDGQSTZJBFJUBT-UHFFFAOYSA-N hypoxanthine Chemical compound O=C1NC=NC2=C1NC=N2 FDGQSTZJBFJUBT-UHFFFAOYSA-N 0.000 description 2
- AGPKZVBTJJNPAG-UHFFFAOYSA-N isoleucine Natural products CCC(C)C(N)C(O)=O AGPKZVBTJJNPAG-UHFFFAOYSA-N 0.000 description 2
- 229960000310 isoleucine Drugs 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 108020004999 messenger RNA Chemical group 0.000 description 2
- 229930182817 methionine Natural products 0.000 description 2
- 230000017074 necrotic cell death Effects 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 description 2
- 229940093430 polyethylene glycol 1500 Drugs 0.000 description 2
- 238000003752 polymerase chain reaction Methods 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- XOJVVFBFDXDTEG-UHFFFAOYSA-N pristane Chemical compound CC(C)CCCC(C)CCCC(C)CCCC(C)C XOJVVFBFDXDTEG-UHFFFAOYSA-N 0.000 description 2
- 102000004196 processed proteins & peptides Human genes 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 208000015347 renal cell adenocarcinoma Diseases 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 238000012216 screening Methods 0.000 description 2
- 210000002966 serum Anatomy 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 208000024891 symptom Diseases 0.000 description 2
- 210000001519 tissue Anatomy 0.000 description 2
- HHLJUSLZGFYWKW-UHFFFAOYSA-N triethanolamine hydrochloride Chemical compound Cl.OCCN(CCO)CCO HHLJUSLZGFYWKW-UHFFFAOYSA-N 0.000 description 2
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 2
- 239000004474 valine Substances 0.000 description 2
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 2
- BJBUEDPLEOHJGE-UHFFFAOYSA-N (2R,3S)-3-Hydroxy-2-pyrolidinecarboxylic acid Natural products OC1CCNC1C(O)=O BJBUEDPLEOHJGE-UHFFFAOYSA-N 0.000 description 1
- YOFPFYYTUIARDI-ZCFIWIBFSA-N (2r)-2-aminooctanedioic acid Chemical compound OC(=O)[C@H](N)CCCCCC(O)=O YOFPFYYTUIARDI-ZCFIWIBFSA-N 0.000 description 1
- BVAUMRCGVHUWOZ-ZETCQYMHSA-N (2s)-2-(cyclohexylazaniumyl)propanoate Chemical compound OC(=O)[C@H](C)NC1CCCCC1 BVAUMRCGVHUWOZ-ZETCQYMHSA-N 0.000 description 1
- MRTPISKDZDHEQI-YFKPBYRVSA-N (2s)-2-(tert-butylamino)propanoic acid Chemical compound OC(=O)[C@H](C)NC(C)(C)C MRTPISKDZDHEQI-YFKPBYRVSA-N 0.000 description 1
- NPDBDJFLKKQMCM-SCSAIBSYSA-N (2s)-2-amino-3,3-dimethylbutanoic acid Chemical compound CC(C)(C)[C@H](N)C(O)=O NPDBDJFLKKQMCM-SCSAIBSYSA-N 0.000 description 1
- UKAUYVFTDYCKQA-UHFFFAOYSA-N -2-Amino-4-hydroxybutanoic acid Natural products OC(=O)C(N)CCO UKAUYVFTDYCKQA-UHFFFAOYSA-N 0.000 description 1
- NHBKXEKEPDILRR-UHFFFAOYSA-N 2,3-bis(butanoylsulfanyl)propyl butanoate Chemical compound CCCC(=O)OCC(SC(=O)CCC)CSC(=O)CCC NHBKXEKEPDILRR-UHFFFAOYSA-N 0.000 description 1
- 102000005946 Acidic Amino Acid Transport Systems Human genes 0.000 description 1
- 108010005990 Acidic Amino Acid Transport Systems Proteins 0.000 description 1
- 108010055672 Amino Acid Transport System L Proteins 0.000 description 1
- 102000000325 Amino Acid Transport System L Human genes 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
- 241000699802 Cricetulus griseus Species 0.000 description 1
- 108700003861 Dominant Genes Proteins 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- CEAZRRDELHUEMR-URQXQFDESA-N Gentamicin Chemical compound O1[C@H](C(C)NC)CC[C@@H](N)[C@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](NC)[C@@](C)(O)CO2)O)[C@H](N)C[C@@H]1N CEAZRRDELHUEMR-URQXQFDESA-N 0.000 description 1
- 229930182566 Gentamicin Natural products 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 description 1
- 108091006905 Human Serum Albumin Proteins 0.000 description 1
- 102000008100 Human Serum Albumin Human genes 0.000 description 1
- PMMYEEVYMWASQN-DMTCNVIQSA-N Hydroxyproline Chemical compound O[C@H]1CN[C@H](C(O)=O)C1 PMMYEEVYMWASQN-DMTCNVIQSA-N 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
- 102000009786 Immunoglobulin Constant Regions Human genes 0.000 description 1
- 108010009817 Immunoglobulin Constant Regions Proteins 0.000 description 1
- 102000012745 Immunoglobulin Subunits Human genes 0.000 description 1
- 108010079585 Immunoglobulin Subunits Proteins 0.000 description 1
- 108010067060 Immunoglobulin Variable Region Proteins 0.000 description 1
- 102000017727 Immunoglobulin Variable Region Human genes 0.000 description 1
- SNDPXSYFESPGGJ-BYPYZUCNSA-N L-2-aminopentanoic acid Chemical compound CCC[C@H](N)C(O)=O SNDPXSYFESPGGJ-BYPYZUCNSA-N 0.000 description 1
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 1
- AHLPHDHHMVZTML-BYPYZUCNSA-N L-Ornithine Chemical compound NCCC[C@H](N)C(O)=O AHLPHDHHMVZTML-BYPYZUCNSA-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
- UKAUYVFTDYCKQA-VKHMYHEASA-N L-homoserine Chemical compound OC(=O)[C@@H](N)CCO UKAUYVFTDYCKQA-VKHMYHEASA-N 0.000 description 1
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 description 1
- SNDPXSYFESPGGJ-UHFFFAOYSA-N L-norVal-OH Natural products CCCC(N)C(O)=O SNDPXSYFESPGGJ-UHFFFAOYSA-N 0.000 description 1
- LRQKBLKVPFOOQJ-YFKPBYRVSA-N L-norleucine Chemical compound CCCC[C@H]([NH3+])C([O-])=O LRQKBLKVPFOOQJ-YFKPBYRVSA-N 0.000 description 1
- 102000052922 Large Neutral Amino Acid-Transporter 1 Human genes 0.000 description 1
- 102000003960 Ligases Human genes 0.000 description 1
- 108090000364 Ligases Proteins 0.000 description 1
- 241001529936 Murinae Species 0.000 description 1
- KNTFCRCCPLEUQZ-VKHMYHEASA-N O-methylserine Chemical compound COC[C@H](N)C(O)=O KNTFCRCCPLEUQZ-VKHMYHEASA-N 0.000 description 1
- 108020005187 Oligonucleotide Probes Proteins 0.000 description 1
- AHLPHDHHMVZTML-UHFFFAOYSA-N Orn-delta-NH2 Natural products NCCCC(N)C(O)=O AHLPHDHHMVZTML-UHFFFAOYSA-N 0.000 description 1
- UTJLXEIPEHZYQJ-UHFFFAOYSA-N Ornithine Natural products OC(=O)C(C)CCCN UTJLXEIPEHZYQJ-UHFFFAOYSA-N 0.000 description 1
- 241000283973 Oryctolagus cuniculus Species 0.000 description 1
- 238000012879 PET imaging Methods 0.000 description 1
- 108090000526 Papain Proteins 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- HCBIBCJNVBAKAB-UHFFFAOYSA-N Procaine hydrochloride Chemical compound Cl.CCN(CC)CCOC(=O)C1=CC=C(N)C=C1 HCBIBCJNVBAKAB-UHFFFAOYSA-N 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- 108010029485 Protein Isoforms Proteins 0.000 description 1
- 102000001708 Protein Isoforms Human genes 0.000 description 1
- 108020004511 Recombinant DNA Proteins 0.000 description 1
- 102400001107 Secretory component Human genes 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 208000026935 allergic disease Diseases 0.000 description 1
- 229940024546 aluminum hydroxide gel Drugs 0.000 description 1
- SMYKVLBUSSNXMV-UHFFFAOYSA-K aluminum;trihydroxide;hydrate Chemical compound O.[OH-].[OH-].[OH-].[Al+3] SMYKVLBUSSNXMV-UHFFFAOYSA-K 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical class N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 238000012197 amplification kit Methods 0.000 description 1
- 239000003708 ampul Substances 0.000 description 1
- 230000001093 anti-cancer Effects 0.000 description 1
- 230000000890 antigenic effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229960000686 benzalkonium chloride Drugs 0.000 description 1
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 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
- 239000011230 binding agent Substances 0.000 description 1
- 239000005082 bioluminescent agent Substances 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000005779 cell damage Effects 0.000 description 1
- 230000010261 cell growth Effects 0.000 description 1
- 208000037887 cell injury Diseases 0.000 description 1
- 230000001876 chaperonelike Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000005081 chemiluminescent agent Substances 0.000 description 1
- 239000013611 chromosomal DNA Substances 0.000 description 1
- 238000010367 cloning Methods 0.000 description 1
- 239000013599 cloning vector Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 239000002872 contrast media Substances 0.000 description 1
- 238000013270 controlled release Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 230000000445 cytocidal effect Effects 0.000 description 1
- 210000000805 cytoplasm Anatomy 0.000 description 1
- 238000002784 cytotoxicity assay Methods 0.000 description 1
- 231100000263 cytotoxicity test Toxicity 0.000 description 1
- 230000034994 death Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 239000000032 diagnostic agent Substances 0.000 description 1
- 229940039227 diagnostic agent Drugs 0.000 description 1
- 238000000502 dialysis Methods 0.000 description 1
- 238000003113 dilution method Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 229910000397 disodium phosphate Inorganic materials 0.000 description 1
- 235000019800 disodium phosphate Nutrition 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000003937 drug carrier Substances 0.000 description 1
- 210000002257 embryonic structure Anatomy 0.000 description 1
- 201000009274 endometriosis of uterus Diseases 0.000 description 1
- 210000003527 eukaryotic cell Anatomy 0.000 description 1
- 230000001605 fetal effect Effects 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 238000010353 genetic engineering Methods 0.000 description 1
- 229960002518 gentamicin Drugs 0.000 description 1
- 229960002897 heparin Drugs 0.000 description 1
- 229920000669 heparin Polymers 0.000 description 1
- 239000000833 heterodimer Substances 0.000 description 1
- 238000005734 heterodimerization reaction 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
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 229960002591 hydroxyproline Drugs 0.000 description 1
- 230000016784 immunoglobulin production Effects 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000001361 intraarterial administration Methods 0.000 description 1
- 230000003834 intracellular effect Effects 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- 238000007912 intraperitoneal administration Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 238000010253 intravenous injection Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- BBJIPMIXTXKYLZ-UHFFFAOYSA-N isoglutamic acid Chemical compound OC(=O)CC(N)CC(O)=O BBJIPMIXTXKYLZ-UHFFFAOYSA-N 0.000 description 1
- 125000000741 isoleucyl group Chemical group [H]N([H])C(C(C([H])([H])[H])C([H])([H])C([H])([H])[H])C(=O)O* 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 210000001165 lymph node Anatomy 0.000 description 1
- 210000004698 lymphocyte Anatomy 0.000 description 1
- 239000012139 lysis buffer Substances 0.000 description 1
- 238000002595 magnetic resonance imaging Methods 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 210000005087 mononuclear cell Anatomy 0.000 description 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
- 239000002773 nucleotide Substances 0.000 description 1
- 125000003729 nucleotide group Chemical group 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 239000002751 oligonucleotide probe Substances 0.000 description 1
- 230000005868 ontogenesis Effects 0.000 description 1
- 229960003104 ornithine Drugs 0.000 description 1
- 229940043515 other immunoglobulins in atc Drugs 0.000 description 1
- 210000001672 ovary Anatomy 0.000 description 1
- 229940055729 papain Drugs 0.000 description 1
- 235000019834 papain Nutrition 0.000 description 1
- 230000005298 paramagnetic effect Effects 0.000 description 1
- 238000010827 pathological analysis Methods 0.000 description 1
- 230000001575 pathological effect Effects 0.000 description 1
- 210000005259 peripheral blood Anatomy 0.000 description 1
- 239000011886 peripheral blood Substances 0.000 description 1
- 238000012831 peritoneal equilibrium test Methods 0.000 description 1
- 229940066827 pertussis vaccine Drugs 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 238000012636 positron electron tomography Methods 0.000 description 1
- 238000012877 positron emission topography Methods 0.000 description 1
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 1
- LWIHDJKSTIGBAC-UHFFFAOYSA-K potassium phosphate Substances [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
- 238000011045 prefiltration Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 229960001309 procaine hydrochloride Drugs 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 230000017854 proteolysis Effects 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 230000009528 severe injury Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 230000019491 signal transduction Effects 0.000 description 1
- 239000007974 sodium acetate buffer Substances 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 210000000278 spinal cord Anatomy 0.000 description 1
- 239000008174 sterile solution Substances 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229940104230 thymidine Drugs 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- BJBUEDPLEOHJGE-IMJSIDKUSA-N trans-3-hydroxy-L-proline Chemical compound O[C@H]1CC[NH2+][C@@H]1C([O-])=O BJBUEDPLEOHJGE-IMJSIDKUSA-N 0.000 description 1
- 230000009261 transgenic effect Effects 0.000 description 1
- 108091005703 transmembrane proteins Proteins 0.000 description 1
- 102000035160 transmembrane proteins Human genes 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 238000010396 two-hybrid screening Methods 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/12—Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells
- A61K35/14—Blood; Artificial blood
- A61K35/17—Lymphocytes; B-cells; T-cells; Natural killer cells; Interferon-activated or cytokine-activated lymphocytes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
- A61K47/6835—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site
- A61K47/6851—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting a determinant of a tumour cell
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K51/00—Preparations containing radioactive substances for use in therapy or testing in vivo
- A61K51/02—Preparations containing radioactive substances for use in therapy or testing in vivo characterised by the carrier, i.e. characterised by the agent or material covalently linked or complexing the radioactive nucleus
- A61K51/04—Organic compounds
- A61K51/08—Peptides, e.g. proteins, carriers being peptides, polyamino acids, proteins
- A61K51/10—Antibodies or immunoglobulins; Fragments thereof, the carrier being an antibody, an immunoglobulin or a fragment thereof, e.g. a camelised human single domain antibody or the Fc fragment of an antibody
- A61K51/1045—Antibodies or immunoglobulins; Fragments thereof, the carrier being an antibody, an immunoglobulin or a fragment thereof, e.g. a camelised human single domain antibody or the Fc fragment of an antibody against animal or human tumor cells or tumor cell determinants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2896—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against molecules with a "CD"-designation, not provided for elsewhere
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/30—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/30—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
- C07K16/3015—Breast
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/30—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
- C07K16/3023—Lung
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/30—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
- C07K16/303—Liver or Pancreas
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/30—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
- C07K16/3038—Kidney, bladder
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/30—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
- C07K16/3046—Stomach, Intestines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/30—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
- C07K16/3053—Skin, nerves, brain
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/30—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
- C07K16/3061—Blood cells
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/30—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
- C07K16/3069—Reproductive system, e.g. ovaria, uterus, testes, prostate
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/574—Immunoassay; Biospecific binding assay; Materials therefor for cancer
- G01N33/57484—Immunoassay; Biospecific binding assay; Materials therefor for cancer involving compounds serving as markers for tumor, cancer, neoplasia, e.g. cellular determinants, receptors, heat shock/stress proteins, A-protein, oligosaccharides, metabolites
- G01N33/57492—Immunoassay; Biospecific binding assay; Materials therefor for cancer involving compounds serving as markers for tumor, cancer, neoplasia, e.g. cellular determinants, receptors, heat shock/stress proteins, A-protein, oligosaccharides, metabolites involving compounds localized on the membrane of tumor or cancer cells
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
- C07K2317/21—Immunoglobulins specific features characterized by taxonomic origin from primates, e.g. man
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
- C07K2317/24—Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
- C07K2317/32—Immunoglobulins specific features characterized by aspects of specificity or valency specific for a neo-epitope on a complex, e.g. antibody-antigen or ligand-receptor
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/54—F(ab')2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/55—Fab or Fab'
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
- C07K2317/565—Complementarity determining region [CDR]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/60—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
- C07K2317/62—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments comprising only variable region components
- C07K2317/622—Single chain antibody (scFv)
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/60—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
- C07K2317/62—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments comprising only variable region components
- C07K2317/624—Disulfide-stabilized antibody (dsFv)
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/60—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
- C07K2317/62—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments comprising only variable region components
- C07K2317/626—Diabody or triabody
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/73—Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/73—Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
- C07K2317/732—Antibody-dependent cellular cytotoxicity [ADCC]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/77—Internalization into the cell
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
- G01N2333/705—Assays involving receptors, cell surface antigens or cell surface determinants
- G01N2333/70596—Molecules with a "CD"-designation not provided for elsewhere in G01N2333/705
Definitions
- the present invention specifically binds to the extracellular region of the LAT1 / CD98 complex, directly inhibits amino acid transport activity, or indirectly induces a cytotoxic factor in cooperation with lymphocytes. Relates to anti-LAT1 / CD98 monoclonal antibody leading to cell death.
- the invention further relates to antibody and / or immunoconjugate compositions and their use in treating, preventing and / or diagnosing tumors.
- Living organisms have various mechanisms for acquiring nutrients and signal transduction substances necessary for life maintenance activities, and transporters and receptors present on various cell membranes are examples.
- transporters and receptors present on various cell membranes are examples.
- amino acids which are the main elements constituting the living body
- molecules responsible for amino acid transport began to be identified, and about 30 types of dominant genes have now been identified.
- These transporters are roughly classified into three types, basic amino acid transporters, neutral amino acid transporters, and acidic amino acid transporters, depending on the nature of the amino acids to be transported.
- the heterodimeric amino acid transporter with CD98 is There are six types including LAT1 to be described.
- LAT1 is a sodium-independent neutral amino acid transporter with relatively wide substrate selectivity over other transporters.
- 4F2hc is a chaperone-like molecule that is linked to a specific transporter and moves to the cell membrane (for example, Yoshikatsu Kanai, Protein Nucleic Acid Enzyme Vol. 46, No. 5, pp. 629-637, 2001 (Non-patent Document 1)) ).
- Non-Patent Document 5 Amino acids are indispensable substances for cell growth, and tumor cells that repeat proliferation in a random manner are considered to require more amino acids than usual. For this reason, it is presumed that the expression level of the amino acid transporter is increased in tumor cells than in normal cells. Therefore, it is suggested that the LAT1 / CD98 complex is useful as a target molecule in the treatment of tumors.
- Japanese Patent Laid-Open No. 2011-24537 Patent Document 1
- the antibody disclosed in Japanese Patent Application Laid-Open No. 2011-24537 has insufficient antibody titer for treating humans and is insufficient for practical use as an antitumor agent.
- anti-LAT1 / CD98 antibody a more excellent antibody that recognizes the extracellular region of the LAT1 / CD98 complex as an epitope.
- the present invention recognizes the extracellular region of the LAT1 / CD98 complex that is highly expressed specifically in tumor cells and inhibits its activity or induces cytotoxic factors to induce tumor cells. Monoclonal antibodies that lead to cell death are provided. Furthermore, the present invention provides a hybridoma that produces the antibody of the present invention, and a complex (immunoconjugate) of the antibody of the present invention and a compound or radioisotope having cell killing activity and / or antitumor activity.
- the present inventors have a CDR amino acid sequence that is different from the CDR amino acid sequence of the anti-LAT1 / CD98 antibody disclosed in JP2011-24537A, and the binding property to the extracellular region of the LAT1 / CD98 complex is significantly superior.
- the anti-LAT1 / CD98 antibody was successfully produced. Further, it was confirmed that the antibody has a remarkable cytotoxicity-inducing activity and internalization activity.
- the present invention provides the following.
- An antibody or antigen-binding fragment thereof that specifically binds to an extracellular region of a LAT1 / CD98 complex of a cell expressing LAT1 / CD98, (1) as light chain complementarity determining region 1 (CDRL1), light chain complementarity determining region 2 (CDRL2), and light chain complementarity determining region 3 (CDRL3), respectively,
- CDRL1 light chain complementarity determining region 1
- CDRL2 light chain complementarity determining region 2
- CDRL3 light chain complementarity determining region 3
- CDRH1 heavy chain complementarity determining region 1
- CDRH2 heavy chain complementarity determining region 2
- CDRH3 heavy chain complementarity determining region 3
- An antibody or an antigen-binding fragment thereof comprising an amino acid sequence or an amino acid sequence each having a mutation of one or several amino acid residues in the amino acid sequences of SEQ ID NO: 10, SEQ ID NO: 11, and SEQ ID NO: 12, (2) As CDRL1, CDRL2, and CDRL3, one or more amino acid sequences of SEQ ID NO: 13, SEQ ID NO: 14, and SEQ ID NO: 15, or amino acid sequences of SEQ ID NO: 13, SEQ ID NO: 14, and SEQ ID NO: 15, respectively.
- An antibody or antigen-binding fragment thereof comprising an amino acid sequence each having a group mutation, (3) As CDRL1, CDRL2, and CDRL3, one or several amino acids in the amino acid sequence of SEQ ID NO: 19, SEQ ID NO: 20, and SEQ ID NO: 21, or SEQ ID NO: 19, SEQ ID NO: 20, and SEQ ID NO: 21, respectively.
- amino acid sequence each having a mutation of the residue, CDRH1, CDRH2, and CDRH3 are one or several amino acids in the amino acid sequences of SEQ ID NO: 22, SEQ ID NO: 23, and SEQ ID NO: 24, or the amino acid sequences of SEQ ID NO: 22, SEQ ID NO: 23, and SEQ ID NO: 24, respectively.
- An antibody or antigen-binding fragment thereof comprising each amino acid sequence having a residue mutation, or (4) the amino acid sequences of SEQ ID NO: 25, SEQ ID NO: 26, and SEQ ID NO: 27, respectively, as CDRL1, CDRL2, and CDRL3, or An amino acid sequence each having a mutation of one or several amino acid residues in the amino acid sequences of SEQ ID NO: 25, SEQ ID NO: 26, and SEQ ID NO: 27; CDRH1, CDRH2, and CDRH3 are one or several amino acids in the amino acid sequences of SEQ ID NO: 28, SEQ ID NO: 29, and SEQ ID NO: 30, or the amino acid sequences of SEQ ID NO: 28, SEQ ID NO: 29, and SEQ ID NO: 30, respectively.
- An antibody or antigen-binding fragment thereof comprising an amino acid sequence each having a residue mutation.
- An antibody or an antigen-binding fragment thereof that specifically binds to an extracellular region of a LAT1 / CD98 complex of a cell expressing LAT1 / CD98, (1) a light chain complementarity determining region 1 (CDRL1) comprising the amino acid sequence of X 1 ASQX 2 VGNNVA (SEQ ID NO: 1), (2) light chain complementarity determining region 2 (CDRL2) comprising the amino acid sequence of YASX 3 RX 4 T (SEQ ID NO: 2), (3) a light chain complementarity determining region 3 (CDRL3) comprising the amino acid sequence of QRX 5 YKSPYT (SEQ ID NO: 3), (4) heavy chain complementarity determining region 1 (CDRH1) comprising the amino acid sequence of GFSLPTSSVS (SEQ ID NO: 4), (5) heavy chain complementarity determining region 2 (CDRH2) comprising the amino acid sequence of VIWSNG
- X 1 is R or K
- X 2 is N or T
- X 3 is S or N
- X 4 is H or N
- X 5 is V or I
- X 6 is A or R
- X 7 is I or F
- X 1 is R, X 2 is N, X 3 is N, X 4 is N, X 5 is I, X 6 is A, X 7 is I, X 8 is D, (2) X 1 is K, X 2 is N, X 3 is S, X 4 is H, X 5 is V, X 6 is R, X 7 is F, X 8 is D, (3) X 1 is K, X 2 is T, X 3 is S, X 4 is H, X 5 is V, X 6 is R, X 7 is F, X 8 is D, or (4) The antibody according to Item [2], wherein X 1 is K, X 2 is N, X 3 is S, X 4 is H, X 5 is V, X 6 is R, X 7 is I, and X 8 is N.
- the antibody or antigen-binding fragment thereof according to any one of items [1] to [7], wherein the subclass is IgG.
- the antigen-binding fragment is Fab, Fab ′, F (ab ′) 2 , scFv, dsFv, ds-scFv, their dimers, minibodies, diabodies, and multimers, or two Item 10.
- the antibody or antigen-binding fragment thereof according to any one of Items [1] to [9], which is a multispecific antibody fragment.
- the antibody or antigen-binding fragment thereof according to any one of items [1] to [10], which is a monoclonal antibody.
- An immunoconjugate comprising the antibody or antigen-binding fragment thereof according to any one of items [1] to [13] and at least one cytotoxic drug, antitumor agent or radioisotope.
- [15] An isolated nucleic acid molecule encoding the antibody or antigen-binding fragment thereof according to any one of items [1] to [14].
- [16] An expression vector comprising the nucleic acid molecule according to item [15].
- [17] A hybridoma cell or a gene-introduced cell containing the nucleic acid molecule according to item [15] or producing the antibody according to any one of items [1] to [13] into which the nucleic acid molecule has been introduced. .
- [18] Specific to the extracellular region of the LAT1 / CD98 complex, comprising culturing the cell of item [17] and collecting an antibody that specifically binds to the LAT1 / CD98 complex from the resulting culture.
- a gene encoding an anti-LAT1 / CD98 monoclonal antibody is isolated from the cell according to item [17], an expression vector containing the gene is constructed, and the expression vector is introduced into a host to express the monoclonal antibody. And collecting the monoclonal antibody that specifically binds to the extracellular region of LAT1 / CD98 from the resulting host, the culture supernatant of the host, or the secretion of the host, specifically to the extracellular region of LAT1 / CD98 A method for producing a binding monoclonal antibody.
- a medicament for preventing or treating a tumor comprising the antibody or antigen-binding fragment thereof or immunoconjugate thereof according to any one of items [1] to [14].
- a composition comprising the antibody according to any one of [1] to [14] or an antigen-binding fragment thereof or an immunoconjugate, wherein the composition expresses LAT1 / CD98-expressing cells.
- the composition to use.
- a method for detecting a tumor comprising reacting the composition according to item [23] with a sample collected from a living body and detecting a reacted signal.
- a method for immunodetecting a tumor in a test tube comprising a step of contacting the composition of item [23] with cancer cells.
- a method for imaging a tumor in vivo comprising a step of administering the composition of item [23] to an individual and a step of obtaining a detection image obtained by near-infrared light imaging, PET, MRI, or ultrasonic imaging.
- a medicament for tumor diagnosis comprising the antibody or antigen-binding fragment or immunoconjugate thereof according to any one of items [1] to [14].
- the tumor is colon cancer, colorectal cancer, lung cancer, breast cancer, brain tumor, melanoma, renal cell cancer, bladder cancer, leukemia, lymphoma, T cell lymphoma, multiple myeloma, gastric cancer, pancreatic cancer, cervix Cancer, endometrial cancer, ovarian cancer, esophageal cancer, liver cancer, squamous cell carcinoma of the head and neck, skin cancer, urinary tract cancer, prostate cancer, choriocarcinoma, pharyngeal cancer, laryngeal cancer, tongue cancer, oral cancer, gallbladder cancer, Thyroid cancer, mesothelioma, pleuromas, male embryos, endometrial hyperplasia, endometriosis, embryonal, fibrosarcoma, Kaposi's sarcoma, hemangioma, spongiform hemangioma, hemangioblastoma, retinoblastoma, Astro
- the antibody of the present invention or an antigen-binding fragment thereof specifically recognizes the extracellular region of the LAT1 / CD98 complex, inhibits the activity of the LAT1 / CD98 complex, or inhibits the cytotoxic factor in cells expressing the LAT1 / CD98 complex. Can induce and cause its cell death. Further, cell death is caused in LAT1 / CD98 complex-expressing cells by immunoconjugate in which the antibody of the present invention or an antigen-binding fragment thereof is bound to a compound having a cell-killing activity and / or an antitumor activity or a radioisotope. Can do.
- the antibody or antigen-binding fragment thereof of the present invention is particularly useful as an anti-cancer antibody drug because it can specifically recognize the extracellular region of the LAT1 / CD98 complex.
- the present invention has a particularly remarkable effect as compared with antibodies that specifically recognize the extracellular region of the LAT1 / CD98 complex reported so far.
- A a human colon cancer cell line (HCT116), a human lung cancer cell line (NCI-H1944, A549), a human cervical cancer cell line (HeLa), an LG9111 monoclonal antibody, an LG9112 monoclonal antibody, an LG9113 monoclonal antibody, an LG9114 monoclonal antibody, It is a figure which shows the binding property of LGtra01-01 monoclonal antibody.
- the red line shows a histogram when each monoclonal antibody is reacted, and the blue line shows a histogram when rat IgG is reacted as Control.
- B The histogram described in (A) is shown by a graph.
- the value indicates a value ( ⁇ MFI) obtained by subtracting MFI of Control from MFI (mean fluorescence intensity) at the time of antibody reaction.
- (A) It is a figure which shows ADCC activity using LG9111 human chimeric antibody and LG9113 human chimeric antibody. Cytotoxicity (%) in the state where 1.25 ⁇ g / mL, 5 ⁇ g / mL, and 20 ⁇ g / mL were added to each human chimeric antibody, and in the state of only effector cells and target cells without any antibody as Control is shown.
- (B) It is a figure which shows ADCC activity with respect to the human colon cancer cell line (HCT116) and human lung cancer cell line (NCI-H1944) of LG9111 human chimeric antibody and LG9113 human chimeric antibody.
- (A) It is a figure which shows the internalization activity of LG9111 monoclonal antibody, LG9112 monoclonal antibody, LG9113 monoclonal antibody, and LG9114 monoclonal antibody.
- (B) It is a figure which shows that the internalization activity shown by (A) is not a false positive by the monoclonal antibody peeling off. Values are 37 ° C. (temperature at which internalization is induced) and 4 ° C. (temperature at which internalization is not induced).
- the MFI of the control reacted with rat IgG from the MFI when the monoclonal antibody was reacted.
- the value obtained by subtracting ( ⁇ MFI) is shown.
- the present invention is directed to an antibody that specifically binds to the extracellular region of the LAT1 / CD98 complex (hereinafter referred to as “anti-antibody”).
- antibody specifically binds to the extracellular region of the LAT1 / CD98 complex
- anti-antibody LAT1 / CD98 antibody
- the present invention provides an antibody and an antigen-binding fragment thereof having an epitope part or all of the amino acid sequence of the extracellular region of the LAT1 / CD98 complex.
- CD98 Information such as the amino acid sequence and mRNA sequence of human CD98 can be obtained from publicly accessible databases such as GenBank with accession numbers such as NP_002385 and NM_002394. Similarly, CD98 for mice and other mammals (eg, rats, cows, etc.) can be obtained from publicly accessible databases.
- LAT1 / CD98 simply refers to a LAT1 / CD98 complex protein.
- the LAT1 protein and the respective genes encoding the CD98 protein may be simply referred to as LAT1 and CD98, in which case, for those skilled in the art, the LAT1 gene and It will be clear that it refers to the CD98 gene.
- LAT1 and CD98 are typically human LAT1 and human CD98, but may be LAT1 and CD98 of mammals other than humans (for example, mouse, rat, bovine, etc.).
- LAT1 / CD98 extracellular region means that when LAT1 / CD98 is expressed on the cell surface, it is exposed on the cell surface opposite to the cytoplasm of the cell membrane (ie, outside the cell). Refers to the LAT1 / CD98 region. Whether or not the antibody of the present invention or the antigen-binding fragment thereof binds to the extracellular region of LAT1 / CD98 was determined using, for example, a human tumor cell line as described in Example 2 of the present specification. This can be confirmed by FCM (abbreviation of Flow Cytomery) analysis.
- FCM abbreviation of Flow Cytomery
- amino acid residues at positions 71 to 83 amino acid residues at positions 141 to 145, and amino acid residues at positions 191 to 198 are used.
- an antibody or an antigen-binding fragment thereof “specifically binds” to the extracellular region of LAT1 / CD98 means that the antibody or antigen-binding fragment has more than their affinity for other amino acid sequences. It binds with a substantially high affinity to a specific amino acid sequence in the region of.
- substantially high affinity means high affinity that allows the specific amino acid sequence to be detected separately from other amino acid sequences by a desired measuring device.
- K a has a coupling constant (K a ) of at least 10 7 M ⁇ 1 , preferably at least 10 8 M ⁇ 1 , more preferably 10 9 M ⁇ 1 , even more preferably 10 10 M ⁇ 1 , 10 11 It means a binding affinity such as M ⁇ 1 , 10 12 M ⁇ 1 or higher, for example up to 10 13 M ⁇ 1 or higher.
- antibody is intended to include all classes and subclasses of intact immunoglobulins.
- antibodies of the invention are of the IgG subclass, and more preferably, is human IgG 1 subclass.
- Antibodies include in particular monoclonal antibodies.
- an “antigen-binding fragment” refers to a fragment having the antigen-binding or variable region of an intact and / or humanized and / or chimeric antibody, such as Fab, Fab ′, Includes F (ab ′) 2 , Fv, ScFv fragments.
- fragments have been produced by proteolysis of intact antibodies, for example by papain degradation (see eg WO 94/29348), but can also be produced directly from transgenic host cells by genetic recombination. .
- the method described in Bird et al. (1988) Science, 242, 423-426 can be used.
- antibody fragments can be generated using the various genetic engineering techniques described below.
- the Fv fragment appears to have a lower interaction energy between its two chains than the Fab fragment.
- these domains are peptides (Bird et al., (1988) Science 242, 423-426, Huston et al., PNAS, 85, 5879-5883), disulfide bridges (Glockshuber et al. (1990) Biochemistry, 29, 1362-1367), and the “knob in hole” mutation (Zhu et al. (1997), Protein Sci., 6, 781-788).
- ScFv fragments can be made by methods well known to those skilled in the art (Whitlow et al., (1991) Methods companion Methods Enzymol, 2, 97-105 and Huston et al. (1993) Int. Rev. Immunol 10, 195-217).
- ScFv can be produced in bacterial cells such as E. coli, but is preferably produced in eukaryotic cells.
- the disadvantage of ScFv is that the product is monovalent, thus making it impossible to increase the binding force due to multivalent bonds, and the short half-life. Attempts to overcome these problems include bivalent (ScFv ′) 2 , which can be obtained from a ScFv containing an additional C-terminal cysteine by chemical coupling (Adams et al.
- ScFv can be multimerized by shortening the peptide linker to 3-12 residues to form a “diabody”. See Holliger et al., PNAS (1993), 90, 6444-6448. By further reducing the linker, ScFv trimers ("Triabody”, see Kortt et al.
- Bispecific diabodies can be made by non-covalent attachment of two single-chain fusion products consisting of a VH domain from another antibody linked to a VL domain of one antibody by a short linker (Kipriyanov). (1998), Int. J. Can 77, 763-772).
- the stability of such a bispecific diabody can be achieved by introducing a disulfide bridge, or by introducing the “knob in hole” mutation described above, or by connecting two hybrid ScFv fragments via a peptide linker. It can be enhanced by forming a chain diabody (ScDb) (see Kontermann et al. (1999) J. Immunol. Methods 226 179-188).
- Tetravalent bispecific molecules are obtained, for example, by fusing a ScFv fragment to the CH3 domain of an IgG molecule or to a Fab fragment via the hinge region (Coloma et al. (1997) Nature Biotechnol. 15 , 159-163).
- tetravalent bispecific molecules have been created by fusion of bispecific single stranded diabodies (see Alt et al. (1999) FEBS Lett 454, 90-94).
- dimerization of ScFv-ScFv tandems with a helix-loop-helix motif-containing linker dimerization of ScFv-ScFv tandems with a helix-loop-helix motif-containing linker (DiBi miniantibody, Muller et al.
- VH and VL antibody variable regions
- Bispecific F (ab ′) 2 fragments can be generated by chemical coupling of Fab ′ fragments or by heterodimerization with leucine zippers (Shalaby et al., (1992) J. Exp. Med. 175, 217-225, and Kostelny et al. (1992), J. Immunol. 148, 1547-1553). Isolated VH and VL domains (Domantis plc) can also be used.
- monoclonal antibody means an antibody (or antibody fragment) obtained from a substantially homogeneous population of antibodies, ie, a naturally occurring individual antibody that comprises the population may be present in small amounts. Identical except for possible mutations. Monoclonal antibodies are highly specific and are directed against a single antigenic site. In contrast to polyclonal antibody preparations that generally contain different antibodies directed against different determinants (epitopes), each monoclonal antibody is directed against a single determinant on the antigen. In addition to their specificity, monoclonal antibodies are advantageous in that they are synthesized by hybridoma culture and are free from contamination by other immunoglobulins.
- the modifier “monoclonal” indicates the character of the antibody as being obtained from a substantially homogeneous population of antibodies, and is not meant to imply that production of the antibody by any particular method is required.
- the monoclonal antibodies used in accordance with the present invention may be made by the hybridoma method first described in Kohler et al., Nature, 256: 495 [1975], or by recombinant DNA methods (eg, US Pat. No. 4, , 816, 567). “Monoclonal antibodies” are also described in, for example, Clackson et al., Nature, 352: 624-628 [1991] and Marks et al., J. MoI. Mol. Biol. 222: 581-597 (1991), including antigen recognition and binding site clones containing antibody fragments (Fv clones) isolated from phage antibody libraries.
- “Monoclonal antibody” includes “chimeric” antibodies (immunoglobulins), which correspond to antibodies whose heavy and / or light chain portions are derived from a particular species or belong to a particular antibody class or subclass. Antibodies that are identical or homologous to the sequence, but the rest of the chain are derived from other species or belong to other antibody classes or subclasses, as long as they exhibit the desired biological activity (Morrison et al., Proc. Natl. Acad. Sci. USA, 81: 6851-6855 [1984]).
- “Humanized” forms of non-human (eg, murine) antibodies are chimeric immunoglobulins, immunoglobulin chains, or fragments thereof (eg, Fv, Fab, Fab ′, etc.) that contain minimal sequence derived from non-human immunoglobulin. F (ab ′) 2 or other antigen-binding sequence of the antibody).
- humanized antibodies are human immunoglobulins (recipient antibodies) whose residues from the recipient CDRs are of non-human species such as mice, rats, rabbits, primates (eg, monkeys). Substituted with residues with the desired specificity, affinity and capacity from the CDR (donor antibody).
- Fv framework region (FR) residues of the human immunoglobulin are replaced with corresponding non-human residues.
- humanized antibodies may comprise residues that are found neither in the recipient antibody nor in the grafted CDR or framework sequences. These modifications are made to further refine and optimize antibody performance.
- a humanized antibody has at least one, typically all, or substantially all of the CDR region corresponding to that of a non-human immunoglobulin and all or substantially all of the FR region is of a human immunoglobulin sequence, typically It can contain substantially all of the two variable domains.
- An optimal humanized antibody may also contain at least a portion of an immunoglobulin constant region (Fc), typically that of a human immunoglobulin.
- Fc immunoglobulin constant region
- “activity of LAT1 / CD98” means neutral amino acid transport activity, amino acid-like drug transport activity, and the like.
- the amino acid transport activity of LAT1 / CD98 can be measured, for example, by intracellular uptake of a labeled amino acid.
- “Inhibiting the activity of LAT1 / CD98” means that the activity of LAT1 / CD98 is significantly reduced or eliminated.
- “significantly reduces or eliminates the activity of LAT1 / CD98” is meant to reduce at least 5% or more of the biological activity of LAT1 / CD98.
- cytotoxic activity means the ability to cause cytotoxicity to cells.
- the antibody of the present invention or an antigen-binding fragment thereof specifically binds to LAT1 / CD98-expressing cells. It shall refer to the ability to bind and induce cytotoxic factors in the cell, leading to cell death or apoptosis.
- the cytotoxic activity can be measured, for example, by the method described in Example 2 of the present invention and evaluated as a cytotoxic rate.
- cell death means “apoptosis”.
- Apoptosis is a function induced by various physiological and pathological factors such as ontogeny programs, death factor stimulation, severe damage to chromosomal DNA due to radiation, severe prescription stress due to abnormal protein accumulation, etc. It is a typical example of active cell death. Contrary to necrosis (necrosis) involving swelling of cell bodies and nuclei, contraction and fragmentation of cell bodies and nuclei occur.
- Examples of the antibodies of the present invention or antigen-binding fragments thereof include (1) a light chain complementarity determining region 1 (CDRL1) comprising the amino acid sequence of SEQ ID NO: 1, (2) light chain complementarity determining region 2 (CDRL2) comprising the amino acid sequence of SEQ ID NO: 2; (3) light chain complementarity determining region 3 (CDRL3) comprising the amino acid sequence of SEQ ID NO: 3; (4) heavy chain complementarity determining region 1 (CDRH1) comprising the amino acid sequence of SEQ ID NO: 4; (5) heavy chain complementarity determining region 2 (CDRH2) comprising the amino acid sequence of SEQ ID NO: 5, and (6) heavy chain complementarity determining region 3 (CDRH3) comprising the amino acid sequence of SEQ ID NO: 6, Or an antigen-binding fragment thereof that specifically binds to the extracellular region of the LAT1 / CD98 complex of cells expressing LAT1 / CD98, including at least one of the above.
- CDRL1 light chain complementarity determining region
- mutant of one or several amino acid residues means one or several (for example, 2, 3, 4, 5) amino acids in the original amino acid sequence. It means that the residue has been deleted, substituted, inserted or added. Due to the presence of such mutation, the target amino acid sequence is, for example, 90% or more, 91% or more, 92% or more, 93% or more, 94% or more, 95% or more, 96% with respect to the original amino acid sequence. Thus, it can have an identity (%) of 97% or more, 98% or more, or 99% or more.
- an antibody having an amino acid sequence having such a mutation at a corresponding position in the original amino acid sequence or an antigen-binding fragment thereof is equivalent to an antibody having the original amino acid sequence or an antigen-binding fragment thereof.
- “equivalent biological activity” includes (i) the ability to bind with specificity to an antigen to which an antibody having an original amino acid sequence or an antigen-binding fragment thereof specifically binds, (ii) The ability of LAT1 / CD98 to inhibit amino acid transport activity, (iii) cytotoxic activity against LAT1 / CD98 on LAT1 / CD98 expressing cells, or (iv) any two or more or all of these Is mentioned.
- “equivalent biological activity” means (iv) above.
- the upper limit of the number of mutated amino acid residues in the above “mutation of one or several amino acid residues” is a criterion for whether or not such equivalent specificity can be maintained (criteria). Limited by.
- amino acids constituting a naturally occurring protein can be grouped according to the characteristics of their side chains.
- amino acids having similar characteristics include aromatic amino acids (tyrosine, phenylalanine). , Tryptophan), basic amino acids (lysine, arginine, histidine), acidic amino acids (aspartic acid, glutamic acid), neutral amino acids (serine, threonine, asparagine, glutamine), amino acids having a hydrocarbon chain (alanine, valine, leucine, It can be classified into groups such as isoleucine, proline) and others (glycine, methionine, cysteine).
- amino acid residues which can be substituted with each other including non-natural amino acids include the following groups, and amino acid residues contained in the same group can be substituted with each other.
- Group A leucine, isoleucine, norleucine, valine, norvaline, alanine, 2-aminobutanoic acid, methionine, o-methylserine, t-butylglycine, t-butylalanine, cyclohexylalanine;
- Group B aspartic acid, glutamic acid, isoaspartic acid , Isoglutamic acid, 2-aminoadipic acid, 2-aminosuberic acid;
- group C asparagine, glutamine;
- group D lysine, arginine, ornithine, 2,4-diaminobutanoic acid, 2,3-diaminopropionic acid;
- group E Proline, 3-hydroxyproline, 4-hydroxyproline;
- Group F serine,
- Preferred examples of the antibody of the present invention or an antigen-binding fragment thereof include (1) as light chain complementarity determining region 1 (CDRL1), light chain complementarity determining region 2 (CDRL2), and light chain complementarity determining region 3 (CDRL3), respectively, An amino acid sequence of No. 9 or an amino acid sequence having a mutation of one or several amino acid residues in the amino acid sequences of SEQ ID No. 7, SEQ ID No. 8 and SEQ ID No.
- CDRL1 light chain complementarity determining region 1
- CDRL2 light chain complementarity determining region 2
- CDRL3 light chain complementarity determining region 3
- LAT1 / CD98 of a cell expressing LAT1 / CD98 comprising an amino acid sequence or an amino acid sequence having a mutation of one or several amino acid residues in the amino acid sequences of SEQ ID NO: 10, SEQ ID NO: 11, and SEQ ID NO: 12, respectively An antibody or antigen-binding fragment thereof that specifically binds to the extracellular region of the complex;
- CDRL1, CDRL2, and CDRL3 one or more amino acid sequences of SEQ ID NO: 13, SEQ ID NO: 14, and SEQ ID NO: 15, or amino acid sequences of SEQ ID NO: 13, SEQ ID NO: 14, and SEQ ID NO: 15, respectively.
- amino acid sequence each having a mutation of one amino acid residue As CDRH1, CDRH2, and CDRH3, one or several amino acid residues are left in the amino acid sequences of SEQ ID NO: 16, SEQ ID NO: 17, and SEQ ID NO: 18, or the amino acid sequences of SEQ ID NO: 16, SEQ ID NO: 17, and SEQ ID NO: 18, respectively.
- An antibody or antigen-binding fragment thereof that specifically binds to an extracellular region of a LAT1 / CD98 complex of a cell expressing LAT1 / CD98, comprising an amino acid sequence each having a group mutation; (3) As CDRL1, CDRL2, and CDRL3, one or several amino acids in the amino acid sequence of SEQ ID NO: 19, SEQ ID NO: 20, and SEQ ID NO: 21, or SEQ ID NO: 19, SEQ ID NO: 20, and SEQ ID NO: 21, respectively.
- amino acid sequence each having a mutation of the residue, CDRH1, CDRH2, and CDRH3 are one or several amino acids in the amino acid sequences of SEQ ID NO: 22, SEQ ID NO: 23, and SEQ ID NO: 24, or the amino acid sequences of SEQ ID NO: 22, SEQ ID NO: 23, and SEQ ID NO: 24, respectively.
- An antibody or antigen-binding fragment thereof that specifically binds to the extracellular region of the LAT1 / CD98 complex of cells expressing LAT1 / CD98 comprising each amino acid sequence having a residue mutation, or (4) CDRL1, CDRL2, And CDRL3, mutations of one or several amino acid residues in the amino acid sequences of SEQ ID NO: 25, SEQ ID NO: 26, and SEQ ID NO: 27, or the amino acid sequences of SEQ ID NO: 25, SEQ ID NO: 26, and SEQ ID NO: 27, respectively
- Each comprising an amino acid sequence having CDRH1, CDRH2, and CDRH3 are one or several amino acids in the amino acid sequences of SEQ ID NO: 28, SEQ ID NO: 29, and SEQ ID NO: 30, or the amino acid sequences of SEQ ID NO: 28, SEQ ID NO: 29, and SEQ ID NO: 30, respectively.
- Examples thereof include an antibody or an antigen-binding fragment thereof that specifically binds to the extracellular region of the LAT1 / CD98 complex of a cell expressing
- preferred examples of the antibody of the present invention or an antigen-binding fragment thereof include (1) including a light chain variable region (LH) comprising an amino acid sequence having 90% or more identity with the amino acid sequence of SEQ ID NO: 31, and an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 31 Heavy chain variable region (VL), (2) including a light chain variable region (LH) comprising an amino acid sequence having 90% or more identity with the amino acid sequence of SEQ ID NO: 33, and an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 34 Heavy chain variable region (VL), (3) including a light chain variable region (LH) comprising an amino acid sequence having 90% or more identity with the amino acid sequence of SEQ ID NO: 35, and an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 36 Heavy chain variable region (VL), or (4) light chain variable region (LH) comprising an amino acid sequence having 90% or more identity with the amino acid sequence of SEQ ID NO: 37, and
- the percentage of the above-mentioned identity is, for example, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100%. possible.
- nucleic Acids Encoding Antibodies of the Invention provides isolated nucleic acid molecules that encode antibodies and antigen-binding fragments thereof that specifically bind to the extracellular region of LAT1 / CD98.
- the nucleic acid molecule is RNA or DNA.
- the nucleic acid molecule of the present invention can be used to produce the antibody of the present invention or an antigen-binding fragment thereof.
- a gene encoding an anti-LAT1 / CD98 monoclonal antibody is isolated from the hybridoma cell of the present invention, an expression vector containing the gene is constructed, and the expression vector is used as a host. And expressing the monoclonal antibody, and collecting the monoclonal antibody that specifically binds to the extracellular region of LAT1 / CD98 from the resulting host, host culture supernatant or host secretion. Methods for producing monoclonal antibodies that specifically bind to the extracellular region of CD98 are provided.
- the DNA encoding the antibody of the present invention or an antigen-binding fragment thereof can be obtained using a conventional method (for example, by using an oligonucleotide probe capable of specifically binding to a gene encoding the heavy and light chains of a mouse antibody. ) Easily separated and sequenced.
- Hybridoma cells producing monoclonal antibodies are a preferred source of such DNA. Once isolated, this DNA is inserted into an expression vector to synthesize monoclonal antibodies in recombinant host cells, which are then used to produce E. coli cells, human HEK293 fetal kidney-derived cells, monkeys that do not produce antibody proteins in other situations.
- telomeres can be transfected into host cells such as COS cells, Chinese hamster ovary (CHO) cells, or myeloma cells.
- host cells such as COS cells, Chinese hamster ovary (CHO) cells, or myeloma cells.
- homologous mouse sequences with sequences of human heavy and light chain constant domains (Morrison et al., Proc. Natl. Acad. Sci., USA, 81: 6851 [1984]
- This DNA may be modified by covalently linking all or part of the coding sequence of the non-immunoglobulin polypeptide to the coding sequence.
- “Chimeric” or “hybrid” antibodies are prepared so as to have the binding specificity of the anti-LAT1 / CD98 monoclonal antibody of the invention.
- the present invention provides an antibody that specifically binds to the extracellular region of LAT1 / CD98 and a hybridoma cell that produces an antigen-binding fragment thereof.
- the present invention also provides a hybridoma containing an antibody that specifically binds to the extracellular region of LAT1 / CD98 and a nucleic acid molecule that encodes an antigen-binding fragment thereof.
- the preparation of the hybridoma cell of the present invention can be specifically performed as follows, but is not limited to this method.
- the spleen is shredded in a serum-free basal medium (hereinafter referred to as a washing medium), centrifuged to collect the cells, treated with Tris-ammonium chloride buffer (pH 7.65) for 2 to 3 minutes and treated with erythrocytes. After being washed with a washing medium, it is provided as a spleen cell for fusion.
- a serum-free basal medium hereinafter referred to as a washing medium
- myeloma cells cell lines obtained from mice are used.
- 8-azaguanine-resistant mouse BALB / c-derived myeloma cell line P3-X63Ag8-U1 (P3-U1) [Current Topics in Microbiology and Immunology-1, European J. Biol. Immunology, 6, 511-519 (1976)]
- SP2 / O-Ag14 SP2 / O-Ag14
- SP-2 [Nature 276, 269-270 (1978)]
- P3-X63-Ag8653 653 [J.
- the extracellular region of LAT1 / CD98 comprising culturing hybridoma cells and collecting an antibody that specifically binds to LAT1 / CD98 from the resulting culture.
- a method for producing a monoclonal antibody that specifically binds to is provided.
- the present invention also provides an immunoconjugate in which an antibody of the present invention and an antigen-binding fragment thereof are combined with a compound having a cell killing activity and / or an antitumor activity or a radioisotope. A conjugate is provided.
- the antibody of the present invention has excellent internalization activity into target tumor cells that express LAT1 / CD98. Therefore, an immunoconjugate to which a compound having cell killing activity and / or antitumor activity is bound can cause these compounds to act directly and selectively on tumor cells.
- the present invention also provides a pharmaceutical composition for preventing or treating or diagnosing a tumor, comprising as an active ingredient the antibody of the present invention or an antigen-binding fragment thereof or an immunoconjugate thereof. Offer things.
- the pharmaceutical composition of the present invention further contains a pharmaceutically acceptable carrier.
- the antibody of the present invention or an antigen-binding fragment thereof specifically binds to the extracellular region of LAT1 / CD98 of cells expressing LAT1 / CD98 (eg, tumor cells),
- LAT1 / CD98 eg, tumor cells
- the activity of LAT1 / CD98 can be inhibited or cytotoxic factors can be induced to cause the cells to die.
- an immunoconjugate to which a compound having cytocidal activity and / or antitumor activity is bound can directly and selectively act these compounds on tumor cells.
- Such compounds include, for example, cytotoxic drugs, antitumor agents, or radioisotopes. Therefore, the pharmaceutical composition of the present invention can prevent tumor cells expressing LAT1 / CD98 on the cell surface, or prevent or treat tumors characterized by such cells and diseases caused by similar mechanisms. Can be used for.
- tumor cancer examples include colon cancer, colorectal cancer, lung cancer, breast cancer, brain tumor, melanoma, renal cell cancer, bladder cancer, leukemia, lymphoma, T cell lymphoma, multiple myeloma, gastric cancer, pancreatic cancer, Cervical cancer, endometrial cancer, ovarian cancer, esophageal cancer, liver cancer, squamous cell carcinoma of the head and neck, skin cancer, urinary tract cancer, prostate cancer, choriocarcinoma, pharyngeal cancer, laryngeal cancer, tongue cancer, oral cancer, gallbladder Cancer, thyroid cancer, mesothelioma, pleuromatous, male embryo, endometrial hyperplasia, endometriosis, embryonal, fibrosarcoma, Kaposi's sarcoma, hemangioma, cavernous hemangioma, hemangioblastoma, retinoblast Tumor, astrocyto
- colon cancer colorectal cancer
- lung cancer breast cancer
- brain tumor bladder cancer
- lymphoma gastric cancer
- pancreatic cancer liver cancer
- prostate cancer a medicine
- the antibody of the present invention or an antigen-binding fragment thereof is used as a medicine, it can be formulated according to conventional means.
- the antibody or antigen-binding fragment thereof can be used parenterally in the form of an injection solution such as a sterile solution or suspension with an aqueous solution or other pharmaceutically acceptable solution,
- the antibody or antigen-binding fragment thereof can be physiologically recognized orally as tablets, capsules, elixirs, microcapsules, etc., after the antibody is converted to IgA and the secretory component is bound and then sugar-coated as necessary
- It can be produced by mixing with known carriers, flavoring agents, excipients, vehicles, preservatives, stabilizers, binders and the like in the unit dosage form generally required for the practice of the formulation.
- the amount of active ingredient in these preparations is such that an appropriate dose within the indicated range can be obtained.
- pharmaceutically acceptable has a reasonable benefit / risk ratio within the scope of normal medical judgment, and does not cause excessive toxicity, irritation, allergic responses, or other problems or complications. Utilized herein to refer to compounds, materials, compositions, and / or dosage forms suitable for use in contact with human and animal tissue, not shown.
- the route of administration of the pharmaceutical composition for the prevention or treatment of the tumor of the present invention can be determined by well-known methods such as intravenous, intraperitoneal, intracerebral, subcutaneous, intramuscular, intraocular, intraarterial, intracerebral spinal cord, or By intralesional injection or infusion, or by controlled release system. Furthermore, as a means for directly administering the antibody or antigen-binding fragment thereof to a tumor site, administration by a catheter or the like is also possible.
- the medicament for preventing or treating tumors of the present invention includes, for example, a buffer (for example, phosphate buffer, sodium acetate buffer), a soothing agent (for example, benzalkonium chloride, procaine hydrochloride, etc.). , Stabilizers (eg, human serum albumin, polyethylene glycol, etc.), preservatives (eg, benzyl alcohol, phenol, etc.), antioxidants, etc.
- a buffer for example, phosphate buffer, sodium acetate buffer
- a soothing agent for example, benzalkonium chloride, procaine hydrochloride, etc.
- Stabilizers eg, human serum albumin, polyethylene glycol, etc.
- preservatives eg, benzyl alcohol, phenol, etc.
- antioxidants e.g, antioxidants, etc.
- the prepared injection solution is usually filled in a suitable ampoule. Since the preparation thus obtained is safe and has low toxicity, it can be administered to mammals including humans.
- the dose of the antibody or antigen-binding fragment thereof or a salt thereof varies depending on the administration subject, symptoms, administration method, etc., but in the case of oral administration, generally, for example, endometriosis patients or uterine adenomyosis patients In (as 60 kg), it is about 0.1 to 100 mg, preferably about 1.0 to 50 mg, more preferably about 1.0 to 20 mg per day.
- the dose varies depending on the subject of administration, symptoms, administration method, etc. For example, in the form of an injection, it is usually about 0.01 per day for a 60 kg patient, for example. About 30 mg, preferably about 0.1-20 mg, more preferably about 0.1-10 mg can be administered by intravenous injection.
- the present invention provides a method for diagnosing a tumor by using a diagnostic immunoconjugate in which at least one diagnostic or detection agent is bound to the above-described antibody of the present invention or an antigen-binding fragment thereof. It is characterized by detecting.
- the diagnostic or detection agent is selected from the group consisting of a radionuclide, a contrast agent, a fluorescent agent, a chemiluminescent agent, a bioluminescent agent, a paramagnetic ion, an enzyme, and a photoactive diagnostic agent.
- a tumor can be detected by reacting a diagnostic immunoconjugate with a sample collected from a living body, such as a tissue fragment or blood, and detecting a signal.
- the measurement method examples include ELISA method, EI method, RIA method, fluorescence immunoassay method, chemiluminescence immunoassay method and the like. In yet another embodiment, it can be used for PET imaging with a diagnostic immunoconjugate to which a diagnostic radionuclide is bound.
- Example 1 Immunization of animals and preparation of antibody-producing cells
- cell lines that highly express LAT1 / CD98 in rats for example, human colon cancer cell line (HCT116)
- antibody-producing cells were collected from the spleen. Immunization was performed by administering 3 ⁇ 10 6 cells as an antigen subcutaneously, intraperitoneally, or intravenously in rats. Antigen administration was performed twice 3 weeks and 6 weeks after the first administration. When the spleen cells were used for fusion with myeloma cells, 3 days after the final administration of the antigen, the spleen was removed from the immunized rat and the spleen cells were collected.
- the spleen is shredded in a serum-free basal medium (hereinafter referred to as a washing medium), centrifuged to collect the cells, treated with Tris-ammonium chloride buffer (pH 7.65) for 2 to 3 minutes and treated with erythrocytes. After washing with a washing medium, it was used as a splenocyte for fusion.
- a serum-free basal medium hereinafter referred to as a washing medium
- Example 2 Production of hybridoma
- the mouse or rat splenocytes obtained in Example 1 (2) and mouse myeloma cell line X63 were mixed at a ratio of 4: 1, centrifuged at 1,200 rpm for 5 minutes, After discarding the supernatant and thoroughly loosening the precipitated cells, at a temperature of 37 ° C.
- Example 3 Antibody screening The hybridoma culture supernatant obtained in Example 1 (3) highly expresses LAT1 / CD98 and is different from the cell line used for the antigen (for example, human lung cancer cell line (NCI- H1944)) and FCM analysis was performed to perform primary screening to determine whether LAT1 / CD98-specific antibodies were produced.
- the FCM reaction was performed in a 96-well plate.
- the LAT1 / CD98 highly expressing cell line was dispensed into tubes in a volume of 50 ⁇ l each at a rate of 2.5 ⁇ 10 5 to 3 ⁇ 10 6 cells / well with PBS. 50 ⁇ l of the hybridoma culture supernatant was added to the cell suspension and reacted at 4 ° C. for 45 minutes.
- LG9111 monoclonal antibody After passing through a prefilter and a membrane filter (0.22 ⁇ m), purification was performed using Protein G Sepharose (GE Healthcare Bioscience), followed by dialysis (3 hours or more ⁇ 4 times) with PBS.
- the resulting four types of anti-LAT1 / CD98 monoclonal antibodies were designated as LG9111 monoclonal antibody, LG9112 monoclonal antibody, LG9113 monoclonal antibody, and LG9114 monoclonal antibody.
- Example 2 Examination of binding ability of monoclonal antibody to tumor cell line The binding ability of anti-LAT1 / CD98 monoclonal antibody was measured by FCM analysis using 4 types of human tumor cell lines.
- the human tumor cell line was adjusted to 1 ⁇ 10 5 cells / well with PBS and dispensed into tubes of 50 ⁇ L each.
- 50 ⁇ L of each monoclonal antibody prepared to 40 ⁇ g / mL was added to the cell suspension, and the mixture was reacted at 4 ° C. for 45 minutes.
- the obtained four types of monoclonal antibodies showed binding activity against various cancer cell lines, and in particular, higher binding activity was observed against the colon cancer cell line HCT116.
- the binding activity was 10 times or more higher than that of the LGtra01-01 monoclonal antibody (the antibody disclosed in Japanese Patent Application Laid-Open No. 2011-24537).
- RNA was isolated from the established anti-LAT1 / CD98 antibody-producing hybridoma strain, and cDNA was synthesized using SMARTer TM RACE cDNA. Amplification Kit (Clontech). From the obtained cDNA, cDNA encoding heavy chain and light chain variable regions was amplified by the polymerase chain reaction (PCR) method and subcloned into a cloning vector. The nucleotide sequence of the obtained cDNA was analyzed, and the amino acid sequences (sequences) of the variable regions of the heavy and light chains of each antibody were determined by a conventional method (described in ⁇ http://www.bioinf.org.uk/abs/>).
- PCR polymerase chain reaction
- CDR sequence-specific primers were synthesized and used to amplify CDRs from the extracted plasmid DNA and incorporated into a human chimeric antibody heavy chain expression vector or a human chimeric antibody light chain expression vector.
- the obtained plasmid was ligated using Ligase to prepare a human chimeric antibody production plasmid.
- human chimeric antibody-producing plasmid was introduced into FreeStyle 293F cells (Invitrogen) and cultured after 96 hours of swirling culture (FreeStyle TM 293 medium, 37 ° C, 8% CO 2 , 135 rpm) The supernatant was obtained. The culture supernatant was purified using Protein G Sepharose (GE Healthcare Bioscience) and then dialyzed with PBS (3 hours or more x 4 times) to obtain a human chimeric LAT1 / CD98 antibody.
- FreeStyle TM MAX Reagent Invitrogen
- Example 4 Examination of antibody-dependent cytotoxic activity by human chimeric antibody Blood was collected from a human into a heparin blood collection tube (Terumo VP-H100K). PBS was added to dilute it twice, and 18 mL of diluted heparinized blood was gently layered on 12 mL of Lymphosepar I (IBL 23010). After centrifugation at 400 g for 30 minutes, the upper plasma layer was gently removed, and the mononuclear cell fraction of the intermediate layer was collected. PBS was added to dilute the mixture twice, and centrifuged at 200 g for 10 minutes to remove the supernatant.
- IBL 23010 Lymphosepar I
- Washing was performed by adding 10 mL of PBS and centrifuging at 200 g for 10 minutes twice, and the cells suspended in 5% FBS-RPMI1640 were used as effector cell suspensions.
- human tumor cells as target cells were suspended in 5% FBS-RPMI1640 so as to be 2 ⁇ 10 5 cells / mL, and 50 ⁇ L each was dispensed to a U-bottom 96-well plate so as to be 1 ⁇ 10 4 cells / well. After adding 50 ⁇ L of human chimeric antibody, the mixture was incubated at 4 ° C. for 15 minutes, centrifuged, and the supernatant was discarded.
- effector cell suspension 100 ⁇ L of effector cell suspension was added (simultaneously, as a control, a well of effector cells only (Effector Spontaneous) and a target cell only well (Target Spontaneous)) were incubated at 37 ° C., 5% CO 2 for 4 hours (as a control at the same time) 45 minutes before completion, a well (Target Max) was prepared by adding 10 ⁇ Lysis buffer to the target cells). After incubation, the mixture was shaken lightly and centrifuged at 200 g for 5 minutes, and 50 ⁇ L of the supernatant was transferred to a flat bottom 96-well plate.
- Cytotoxicity (%) (Experimental-Effector Spontaneous-Target Spontaneous) / (Target Max-Target Spontaneous) x 100. As shown in FIG.
- Example 5 Examination of Internalization Activity of Monoclonal Antibody The internalization activity of anti-LAT1 / CD98 monoclonal antibody was measured by FCM analysis using a human tumor cell line.
- the human colon cancer cell line HCT116 was suspended in 0.1% BSA-PBS, and 50 ⁇ L was dispensed into a U-bottom 96-well plate at 1 ⁇ 10 5 cells / well.
- 50 ⁇ L of each monoclonal antibody prepared to 20 ⁇ g / mL was added and reacted at 4 ° C. for 45 minutes. Washing by adding 150 ⁇ L of 0.1% BSA-PBS and centrifuging at 500 g for 3 minutes at 4 ° C.
- the PE-labeled anti-Rat IgG was reacted with the cell pellet in the same manner. After washing, the cells were incubated at 37 ° C. (temperature at which internalization was induced) or 4 ° C. (temperature at which internalization was not induced), respectively, for 1 hour. After washing, the same measurement was performed with FACSCalibur. As shown in FIG. 3 (B), no difference in fluorescence intensity was observed between the case of incubation at 4 ° C. and the case of incubation at 37 ° C.
- the anti-LAT1 / CD98 antibody of the present invention is markedly superior to the extracellular region of the LAT1 / CD98 complex as compared to the anti-LAT1 / CD98 antibodies reported so far. And has excellent cytotoxic activity against cells expressing the LAT1 / CD98 complex.
- the present invention is useful for inducing apoptosis of tumor cells that highly express LAT1 / CD98, or for pathological analysis, prevention, treatment, etc. of tumors characterized by tumor cells that highly express LAT1 / CD98.
- LG9111 light chain complementarity determining region 1 (CDRL1) SEQ ID NO: 8 LG9111 light chain complementarity determining region 2 (CDRL2) SEQ ID NO: 9 LG9111 light chain complementarity determining region 3 (CDRL3) SEQ ID NO: 10 LG9111 heavy chain complementarity determining region 1 (CDRH1) SEQ ID NO: 11 LG9111 heavy chain complementarity determining region 2 (CDRH2) SEQ ID NO: 12 LG9111 heavy chain complementarity determining region 3 (CDRH3) SEQ ID NO: 13 LG9112 light chain complementarity determining region 1 (CDRL1) SEQ ID NO: 14 LG9112 light chain complementarity determining region 2 (CDRL2) SEQ ID NO: 15 LG9112 light chain complementarity determining region 3 (CDRL3) SEQ ID NO: 16 LG9112 heavy chain complementarity determining region 1 (CDRH1) SEQ ID NO: 17 LG9112 heavy chain complementarity determining region 2 (CDRH2) SEQ ID NO: 18 LG91
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Immunology (AREA)
- Cell Biology (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biochemistry (AREA)
- Engineering & Computer Science (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Hematology (AREA)
- Biomedical Technology (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Oncology (AREA)
- Epidemiology (AREA)
- Urology & Nephrology (AREA)
- Physics & Mathematics (AREA)
- Biotechnology (AREA)
- Food Science & Technology (AREA)
- Developmental Biology & Embryology (AREA)
- Optics & Photonics (AREA)
- Hospice & Palliative Care (AREA)
- Microbiology (AREA)
- Virology (AREA)
- Zoology (AREA)
- Analytical Chemistry (AREA)
- General Physics & Mathematics (AREA)
- Pathology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pregnancy & Childbirth (AREA)
- Reproductive Health (AREA)
- Gynecology & Obstetrics (AREA)
- Gastroenterology & Hepatology (AREA)
Abstract
Description
[1]LAT1/CD98を発現する細胞のLAT1/CD98複合体の細胞外領域に特異的に結合する抗体またはその抗原結合断片であって、
(1)軽鎖相補性決定領域1(CDRL1)、軽鎖相補性決定領域2(CDRL2)、および軽鎖相補性決定領域3(CDRL3)として、それぞれ、配列番号7、配列番号8、および配列番号9のアミノ酸配列、または配列番号7、配列番号8、および配列番号9のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含み、
重鎖相補性決定領域1(CDRH1)、重鎖相補性決定領域2(CDRH2)、および重鎖相補性決定領域3(CDRH3)として、それぞれ、配列番号10、配列番号11、および配列番号12のアミノ酸配列、もしくは配列番号10、配列番号11、および配列番号12のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含む、抗体またはその抗原結合断片、
(2)CDRL1、CDRL2、およびCDRL3として、それぞれ、配列番号13、配列番号14、および配列番号15のアミノ酸配列、もしくは配列番号13、配列番号14、および配列番号15のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含み、
CDRH1、CDRH2、およびCDRH3として、それぞれ、配列番号16、配列番号17、配列番号18のアミノ酸配列、もしくは配列番号16、配列番号17、および配列番号18のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含む、抗体またはその抗原結合断片、
(3)CDRL1、CDRL2、およびCDRL3として、それぞれ、配列番号19、配列番号20、および配列番号21、もしくは配列番号19、配列番号20、および配列番号21のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含み、
CDRH1、CDRH2、およびCDRH3として、それぞれ、配列番号22、配列番号23、および配列番号24のアミノ酸配列、もしくは配列番号22、配列番号23、および配列番号24のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異を有する各アミノ酸配列を含む、抗体またはその抗原結合断片、または
(4)CDRL1、CDRL2、およびCDRL3として、それぞれ、配列番号25、配列番号26、および配列番号27のアミノ酸配列、もしくは配列番号25、配列番号26、および配列番号27のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含み、
CDRH1、CDRH2、およびCDRH3として、それぞれ、配列番号28、配列番号29、および配列番号30のアミノ酸配列、もしくは配列番号28、配列番号29、および配列番号30のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含む、抗体またはその抗原結合断片。
[2]LAT1/CD98を発現する細胞のLAT1/CD98複合体の細胞外領域に特異的に結合する抗体またはその抗原結合断片であって、
(1)X1ASQX2VGNNVA(配列番号1)のアミノ酸配列を含む軽鎖相補性決定領域1(CDRL1)、
(2)YASX3RX4T(配列番号2)のアミノ酸配列を含む軽鎖相補性決定領域2(CDRL2)、
(3)QRX5YKSPYT(配列番号3)のアミノ酸配列を含む軽鎖相補性決定領域3(CDRL3)、
(4)GFSLPTSSVS(配列番号4)のアミノ酸配列を含む重鎖相補性決定領域1(CDRH1)、
(5)VIWSNGNTDYSSX6X7KS(配列番号5)のアミノ酸配列を含む重鎖相補性決定領域2(CDRH2)、および
(6)NFRNX8PGVMDA(配列番号6)のアミノ酸配列を含む重鎖相補性決定領域3(CDRH3)
(但し、X1~X8は、任意の天然に存在するアミノ酸残基である)
を含む、抗体またはその抗原結合断片。
[3]X1が、RまたはKであり、
X2が、NまたはTであり、
X3が、SまたはNであり、
X4が、HまたはNであり、
X5が、VまたはIであり、
X6が、AまたはRであり、
X7が、IまたはFである、
X8が、DまたはNである、項[2]に記載の抗体またはその抗原結合断片。
[4](1)X1がR、X2がN、X3がN、X4がN、X5がI、X6がA、X7がI、X8がDであるか、
(2)X1がK、X2がN、X3がS、X4がH、X5がV、X6がR、X7がF、X8がDであるか、
(3)X1がK、X2がT、X3がS、X4がH、X5がV、X6がR、X7がF、X8がDであるか、または
(4)X1がK、X2がN、X3がS、X4がH、X5がV、X6がR、X7がI、X8がNである、項[2]に記載の抗体またはその抗原結合断片。
[5]項[1]~[4]のいずれか一項に記載の抗体またはその抗原結合断片であって、
(1)配列番号31のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む軽鎖可変領域(LH)、および
配列番号31のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む重鎖可変領域(VL)、
(2)配列番号33のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む軽鎖可変領域(LH)、および
配列番号34のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む重鎖可変領域(VL)、
(3)配列番号35のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む軽鎖可変領域(LH)、および
配列番号36のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む重鎖可変領域(VL)、または
(4)配列番号37のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む軽鎖可変領域(LH)、および
配列番号38のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む重鎖可変領域(VL)、
を含有する、抗体もしくはその抗原結合断片。
[6]項[1]~[5]のいずれか一項に記載の抗体もしくはその抗原結合断片であって、
(1)配列番号31のアミノ酸配列を含む軽鎖可変領域(VL)、および
配列番号32のアミノ酸配列を含む重鎖可変領域(VH)、
(2)配列番号33のアミノ酸配列を含む軽鎖可変領域(VL)、および
配列番号34のアミノ酸配列を含む重鎖可変領域(VH)、
(3)配列番号35のアミノ酸配列を含む軽鎖可変領域(VL)、および
配列番号36のアミノ酸配列を含む重鎖可変領域(VH)、または
(4)配列番号37のアミノ酸配列を含む軽鎖可変領域(VL)、および
配列番号38のアミノ酸配列を含む重鎖可変領域(VH)、
を含有する、抗体もしくはその抗原結合断片。
[7]LAT1/CD98を発現する細胞に対する細胞障害活性および/またはインターナリゼーション活性を有する、項[1]~[6]のいずれか一項に記載の抗体またはその抗原結合断片。
[8]サブクラスがIgGである、項[1]~[7]のいずれか一項に記載の抗体またはその抗原結合断片。
[9]上記IgGが、IgG2aまたはIgG1である、項[8]に記載の抗体またはその抗原結合断片。
[10]上記抗原結合断片が、Fab、Fab’、F(ab’)2、scFv、dsFv、ds-scFv、それらのダイマー、ミニボディ(minobodies)、ダイアボディ(diabodies)、およびマルチマー、または二重特異性抗体断片である、項[1]~[9]のいずれか一項に記載の抗体またはその抗原結合断片。
[11]モノクローナル抗体である、項[1]~[10]のいずれか一項に記載の抗体またはその抗原結合断片。
[12]ラット、マウス、霊長類、またはヒト抗体である、項[1]~[11]のいずれか一項に記載の抗体またはその抗原結合断片。
[13]キメラ抗体またはヒト化抗体である、項[1]~[11]のいずれか一項に記載の抗体またはその抗原結合断片。
[14]項[1]~[13]のいずれか一項に記載の抗体またはその抗原結合断片と少なくとも1つの細胞毒性薬、抗腫瘍剤または放射性同位体を含んでなるイムノコンジュゲート。
[15]項[1]~[14]のいずれか一項に記載の抗体またはその抗原結合断片をコードする単離された核酸分子。
[16]項[15]に記載の核酸分子を含む発現ベクター。
[17]項[15]に記載の核酸分子を含むかまたは該核酸分子を導入した、項[1]~[13]のいずれか一項に記載の抗体を産生する、ハイブリドーマ細胞または遺伝子導入細胞。
[18]項[17]に記載の細胞を培養し、得られる培養物からLAT1/CD98複合体に特異的に結合する抗体を採取することを含む、LAT1/CD98複合体の細胞外領域に特異的に結合するモノクローナル抗体の製造方法。
[19]項[17]に記載の細胞から抗LAT1/CD98モノクローナル抗体をコードする遺伝子を単離し、該遺伝子を含む発現ベクターを構築し、該発現ベクターを宿主に導入して上記モノクローナル抗体を発現せしめ、得られる宿主、宿主の培養上清または宿主の分泌物からLAT1/CD98の細胞外領域に特異的に結合するモノクローナル抗体を採取することを含む、LAT1/CD98の細胞外領域に特異的に結合するモノクローナル抗体の製造方法。
[20]上記宿主が、大腸菌、酵母細胞、昆虫細胞、哺乳動物細胞、植物細胞、または哺乳動物である、項[19]に記載の製造方法。
[21]項[1]~[14]のいずれか一項に記載の抗体またはその抗原結合断片またはイムノコンジュゲートを含有する組成物であって、LAT1/CD98を発現する細胞に適用して該細胞のアポトーシスを誘導するために使用する、組成物。
[22]項[1]~[14]のいずれか一項に記載の抗体またはその抗原結合断片またはイムノコンジュゲートを含有する、腫瘍の予防または治療のための医薬。
[23]項[1]~[14]のいずれか一項に記載の抗体またはその抗原結合断片またはイムノコンジュゲートを含有する組成物であって、LAT1/CD98を発現する細胞を検出するために使用する、組成物。
[24]項[23]の組成物と、生体から採取された試料とを反応させ、反応したシグナルを検出することを特徴とする、腫瘍の検出方法。
[25]項[23]の組成物を癌細胞と接触する工程を含む試験管内の腫瘍の免疫検出方法。
[26]項[23]の組成物を個体に投与する工程および近赤外光イメージング、PET、MRIまたは超音波イメージングによって得られる検出映像を得る工程を含む生体内で腫瘍の映像化方法。
[27]項[1]~[14]のいずれか一項に記載の抗体またはその抗原結合断片またはイムノコンジュゲートを含有する、腫瘍の診断のための医薬。
[28]上記腫瘍が、大腸癌、結腸直腸癌、肺癌、乳癌、脳腫瘍、黒色腫、腎細胞癌、膀胱癌、白血病、リンパ腫、T細胞リンパ腫、多発性骨髄腫、胃癌、膵臓癌、子宮頸癌、子宮内膜癌、卵巣癌、食道癌、肝臓癌、頭頸部扁平上皮癌、皮膚癌、尿路癌、前立腺癌、絨毛癌、咽頭癌、喉頭癌、舌癌、口腔癌、胆嚢癌、甲状腺癌、中皮腫、胸膜腫、男性胚腫、子宮内膜過形成、子宮内膜症、胚芽腫、線維肉腫、カポジ肉腫、血管腫、海綿状血管腫、血管芽腫、網膜芽腫、星状細胞腫、神経線維腫、稀突起謬腫、髄芽腫、神経芽腫、神経膠腫、横紋筋肉腫、謬芽腫、骨原性肉腫、平滑筋肉腫、甲状肉腫、およびウィルムス腫瘍からなる群から選択される少なくとも1つである、項[22]または項[27]に記載の医薬。
[29]以下の(1)~(6)からなる群から選択される相補性決定領域(CDR):
(1)配列番号7、13、19、または25のアミノ酸配列を含む軽鎖相補性決定領域1(CDRL1)、
(2)配列番号8、14、20、または26のアミノ酸配列を含む軽鎖相補性決定領域2(CDRL2)、
(3)配列番号9、15、21、または27のアミノ酸配列を含む軽鎖相補性決定領域3(CDRL3)、
(4)配列番号10、16、22、または28のアミノ酸配列を含む重鎖相補性決定領域1(CDRH1)、
(5)配列番号11、17、23、または29のアミノ酸配列を含む重鎖相補性決定領域2(CDRH2)、および
(6)配列番号12、18、24、または30のアミノ酸配列を含む重鎖相補性決定領域3(CDRH3)。
本発明は、1つの実施形態において、LAT1/CD98複合体の細胞外領域に特異的に結合する抗体(本明細書中、「抗LAT1/CD98抗体」と呼ぶこともある。)およびその抗原結合断片を提供する。すなわち、本発明は、LAT1/CD98複合体の細胞外領域のアミノ酸配列の一部または全部をエピトープとする抗体およびその抗原結合断片を提供する。
ヒトLAT1と細胞膜上で複合体を形成する「ヒトCD98」は、630アミノ酸残基からなる1回膜貫通II型の膜タンパク質である。ヒトCD98のアミノ酸配列、mRNA配列等の情報は、それぞれNP_002385、NM_002394等のアクセッション番号でGenBank等の公にアクセス可能なデータベースから入手することができる。また、マウスや他の哺乳動物(例えば、ラット、ウシなど)のCD98も同様に、公にアクセス可能なデータベースから入手することができる。
(1)配列番号:1のアミノ酸配列を含む軽鎖相補性決定領域1(CDRL1)、
(2)配列番号:2のアミノ酸配列を含む軽鎖相補性決定領域2(CDRL2)、
(3)配列番号:3のアミノ酸配列を含む軽鎖相補性決定領域3(CDRL3)、
(4)配列番号:4のアミノ酸配列を含む重鎖相補性決定領域1(CDRH1)、
(5)配列番号:5のアミノ酸配列を含む重鎖相補性決定領域2(CDRH2)、および
(6)配列番号:6のアミノ酸配列を含む重鎖相補性決定領域3(CDRH3)、
のうちの少なくとも1つを含む、LAT1/CD98を発現する細胞のLAT1/CD98複合体の細胞外領域に特異的に結合する抗体またはその抗原結合断片が挙げられる。
(1)軽鎖相補性決定領域1(CDRL1)、軽鎖相補性決定領域2(CDRL2)、および軽鎖相補性決定領域3(CDRL3)として、それぞれ、配列番号7、配列番号8、および配列番号9のアミノ酸配列、または配列番号7、配列番号8、および配列番号9のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含み、
重鎖相補性決定領域1(CDRH1)、重鎖相補性決定領域2(CDRH2)、および重鎖相補性決定領域3(CDRH3)として、それぞれ、配列番号10、配列番号11、および配列番号12のアミノ酸配列、もしくは配列番号10、配列番号11、および配列番号12のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含む、LAT1/CD98を発現する細胞のLAT1/CD98複合体の細胞外領域に特異的に結合する抗体またはその抗原結合断片、
(2)CDRL1、CDRL2、およびCDRL3として、それぞれ、配列番号13、配列番号14、および配列番号15のアミノ酸配列、もしくは配列番号13、配列番号14、および配列番号15のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含み、
CDRH1、CDRH2、およびCDRH3として、それぞれ、配列番号16、配列番号17、配列番号18のアミノ酸配列、もしくは配列番号16、配列番号17、および配列番号18のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含む、LAT1/CD98を発現する細胞のLAT1/CD98複合体の細胞外領域に特異的に結合する抗体またはその抗原結合断片、
(3)CDRL1、CDRL2、およびCDRL3として、それぞれ、配列番号19、配列番号20、および配列番号21、もしくは配列番号19、配列番号20、および配列番号21のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含み、
CDRH1、CDRH2、およびCDRH3として、それぞれ、配列番号22、配列番号23、および配列番号24のアミノ酸配列、もしくは配列番号22、配列番号23、および配列番号24のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異を有する各アミノ酸配列を含む、LAT1/CD98を発現する細胞のLAT1/CD98複合体の細胞外領域に特異的に結合する抗体またはその抗原結合断片、または
(4)CDRL1、CDRL2、およびCDRL3として、それぞれ、配列番号25、配列番号26、および配列番号27のアミノ酸配列、もしくは配列番号25、配列番号26、および配列番号27のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含み、
CDRH1、CDRH2、およびCDRH3として、それぞれ、配列番号28、配列番号29、および配列番号30のアミノ酸配列、もしくは配列番号28、配列番号29、および配列番号30のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含む、LAT1/CD98を発現する細胞のLAT1/CD98複合体の細胞外領域に特異的に結合する抗体またはその抗原結合断片が挙げられる。
(1)配列番号31のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む軽鎖可変領域(LH)、および
配列番号31のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む重鎖可変領域(VL)、
(2)配列番号33のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む軽鎖可変領域(LH)、および
配列番号34のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む重鎖可変領域(VL)、
(3)配列番号35のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む軽鎖可変領域(LH)、および
配列番号36のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む重鎖可変領域(VL)、または
(4)配列番号37のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む軽鎖可変領域(LH)、および
配列番号38のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む重鎖可変領域(VL)、
を含有する、LAT1/CD98を発現する細胞のLAT1/CD98複合体の細胞外領域に特異的に結合する抗体もしくはその抗原結合断片が挙げられる。
本発明は、別の実施形態において、LAT1/CD98の細胞外領域に特異的に結合する抗体およびその抗原結合断片をコードする単離された核酸分子を提供する。核酸分子は、RNAまたはDNAである。本発明の核酸分子は、本発明の抗体またはその抗原結合断片を作製するために使用することができる。
本発明はさらに別の実施形態において、LAT1/CD98の細胞外領域に特異的に結合する抗体およびその抗原結合断片を産生するハイブリドーマ細胞を提供する。本発明はまた、LAT1/CD98の細胞外領域に特異的に結合する抗体およびその抗原結合断片をコードする核酸分子を含有するハイブリドーマを提供する。
抗LAT1/CD98モノクローナル抗体を作製するために必要な抗原としては、LAT1/CD98を産生する細胞あるいはその細胞画分等を用いることができる。
6~24週令のマウスまたはラットに、(1)に示した方法で作製された抗原を免疫して、その動物の脾、リンパ節、末梢血より抗体産生細胞を採取する。免疫は、動物の皮下あるいは静脈内あるいは腹腔内に、適当なアジュバント〔例えば、フロインドの完全アジュバントまたは、水酸化アルミニウムゲルと百日咳菌ワクチンなど〕とともに抗原を投与することにより行う。抗原の投与は、1回目の投与の後2~3週間おきに3~7回行う。各投与後5~10日目に眼底静脈叢より採血し、その血清が抗原と反応することを酵素免疫測定法〔酵素免疫測定法(ELISA法):医学書院刊 1976年〕などで調べる。抗原に対し、その血清が十分な抗体価を示したマウスまたはラットを抗体産生細胞の供給源として供する。脾細胞を骨髄腫細胞との融合に供するにあたって、抗原物質の最終投与後3~4日目に、免疫したマウスまたはラットより脾臓を摘出し、脾細胞を採取する。脾臓を血清無添加の基礎培地(以下洗浄用培地という。)中で細断し、遠心分離して細胞を回収後、トリス-塩化アンモニウム緩衝液(pH7.65)で2~3分間処理し赤血球の除去を行い、洗浄用培地で洗浄した後に融合用脾細胞として提供する。
骨髄腫細胞としては、マウスから得られた株化細胞を使用する。たとえば、8-アザグアニン耐性マウス(BALB/c由来)骨髄腫細胞株P3-X63Ag8-U1(P3-U1)〔Current Topics in Microbiology and Immunology-1、European J. Immunology, 6, 511-519(1976)〕、SP2/O-Ag14(SP-2)〔Nature 276, 269-270 (1978)〕、P3-X63-Ag8653(653)〔J.Immunology 123, 1548-1550 (1979)〕、P3-X63-Ag8(X63)〔Nature 256, 495-497 (1975)〕などが用いられる。これらの細胞株は、8-アザグアニン培地〔RPMI-1640培地にグルタミン(1.5mM)、2-メルカプトエタノール(5×10-5M)、ジェンタマイシン(10μg/ml)および牛胎児血清(FCS)を10%加えた培地(以下、正常培地という。)に、さらに8-アザグアニン(15μg/ml)を加えた培地〕で継代するが、細胞融合の3~4日前に正常培地に継代し、融合当日2×107個以上の細胞数を確保する。
(2)で免疫した抗体産生細胞と(3)で得られた骨髄腫細胞を洗浄用培地またはPBS(リン酸二ナトリウム1.83g、リン酸一カリウム0.21g、食塩7.65g、蒸留水1リットル、pH7.2)でよく洗浄し、細胞数が、抗体産生細胞:骨髄腫細胞=5~10:1になるよう混合させる。細胞回収後、細胞をよくほぐし、攪拌しながら、37℃で、ポリエチレングライコール-1,500(PEG-1,500)2g、洗浄用培地2mlおよびジメチルスルホキシド0.7mlの混液0.2~1ml/108抗体産生細胞を加え、1~2分間毎に洗浄用培地1~2mlを数回加え、全量が50mlになるまで洗浄する。細胞回収後、ゆるやかに細胞をほぐしながら、HAT培地〔正常培地にヒポキサンチン(10-4M)、チミジン(1.5×10-5M)およびアミノプテリン(4×10-7M)を加えた培地〕100ml中に懸濁する。この懸濁液を96ウェル培養用プレートに100μl/ウェルずつ分注し、5%CO2インキュベーター中、37℃で7~14日間培養する。培養後、培養上清の一部をとり、例えばFACS(Fluorescence-Activated Cell Sortingの略)などを用いて、LAT1/CD98タンパク質に特異的に反応する抗体を選択する。ついで、限界希釈法によりクローニングを2回繰り返し〔1回目は、HT培地(HAT培地からアミノプテリンを除いた培地)、2回目は、正常培地を使用する〕、安定して強い抗体価の認められたものを抗LAT1/CD98モノクローナル抗体産生ハイブリドーマ株として選択する。
本発明はまた、別の実施形態において、本発明の抗体およびその抗原結合断片に殺細胞活性および/または抗腫瘍活性を有する化合物あるいは放射性同位体を結合させたイムノコンジュゲートを提供する。
本発明はまた、さらに別の実施形態において、本発明の抗体またはその抗原結合断片またはそれらとのイムノコンジュゲートを有効成分として含有する、腫瘍の予防または治療または診断のための医薬組成物を提供する。本発明の医薬組成物は、さらに薬学的に許容し得る担体を含有する。
本発明はまた、さらに別の実施形態において、上記の本発明の抗体またはその抗原結合断片に少なくとも1つの診断または検出剤を結合した診断用イムノコンジュゲートにより、腫瘍を検出することを特徴とする。好ましくは、診断または検出剤は、放射性核種、造影剤、蛍光剤、化学発光剤、生物発光剤、常磁性イオン、酵素、および光活性診断剤からなる群から選択される。1つの実施形態では、診断用イムノコンジュゲートと生体から採取された試料、例えば組織片または血液等と反応させ、シグナルを検出することにより、腫瘍を検出することができる。測定法としては、例えばELISA法、EI法、RIA法、蛍光免疫測定法、化学発光免疫測定法等が挙げられる。また別の実施形態では、診断用放射性核種を結合させた診断用イムノコンジュゲートによるPETイメージングに使用することができる。
(1)動物の免疫と抗体産生細胞の調製
抗LAT1/CD98モノクローナル抗体を作製するために、ラットに、LAT1/CD98を高発現している細胞株(例えば、ヒト大腸癌細胞株(HCT116))を免疫して、その脾臓より抗体産生細胞を採取した。免疫は、ラットの皮下、腹腔、または静脈内に抗原として細胞3×106個を投与することにより行った。抗原の投与は、1回目の投与の3週間後および6週間後に2回行った。脾細胞を骨髄腫細胞との融合に供するにあたって、抗原の最終投与後3日後に、免疫したラットより脾臓を摘出し脾細胞を採取した。脾臓を血清無添加の基礎培地(以下洗浄用培地という。)中で細断し、遠心分離して細胞を回収後、トリス-塩化アンモニウム緩衝液(pH7.65)で2~3分間処理し赤血球の除去を行い、洗浄用培地で洗浄した後に融合用脾細胞として用いた。
実施例1(2)で得られたマウスまたはラット脾細胞とマウス骨髄腫細胞株X63とを4:1の比率で混合し、1,200rpmで5分間遠心した後、上清を捨て、沈澱した細胞群をよくほぐした後、攪拌しながら、37℃で、ポリエチレングライコール-1500(PEG-1500)2g、DMEM培地2mlおよびジメチルスルホキシド0.7mlの混液を0.2~1ml/108個マウス脾細胞の割合で加え、さらに1~2分間毎にDMEM培地1~2mlを数回加えた後、DMEM培地を加えて全量が50mlになるようにした。900rpmで5分間遠心し、上清を捨てHAT培地100ml中に細胞をゆるやかに懸濁した。この懸濁液を96ウェル培養用プレートに100μl/ウェルずつ分注し、5%CO2インキュベーター中、37℃で10~14日間培養した。
実施例1(3)で得られたハイブリドーマ培養上清をLAT1/CD98を高発現し、かつ抗原に用いた細胞株とは異なる細胞株(例えば、ヒト肺癌細胞株(NCI-H1944))と反応させ、FCM解析を行うことによりLAT1/CD98特異的抗体を産生しているかの1次スクリーニングを行った。
FCMの反応は96ウェルプレートにて行った。LAT1/CD98高発現細胞株をPBSにて2.5×105~3×106個/ウェルになるように50μlずつチューブに分注した。この細胞浮遊液にハイブリドーマの培養上清50μlを加え、4℃で45分反応させた。0.1%BSA-PBS100μLを加え、500gで3分間、4℃で遠心する洗浄を3回行い、細胞ペレットに200倍希釈したPE-labeled anti Rat IgG(Jackson Immuno Research)を50μL加え、遮光状態で4℃で45分間反応させた。0.1%BSA-PBS100μLを加え、500gで3分間、4℃で遠心する洗浄を3回行い、PBS500μLに懸濁し、FCMチューブに移した。死細胞を除くため測定直前にPI100μLを添加し、FACSCalibur(Becton Dickinson)にて測定した。陽性反応が得られたクローンを選別し、4種の抗LAT1/CD98抗体産生ハイブリドーマ株(LG9111、LG9112、LG9113およびLG9114)を樹立した。
プリスタン処理した8週令ヌード雄マウス(KSN)に実施例1(4)で得られたハイブリドーマ株を1×107細胞/匹それぞれ腹腔内注射した。10~15日後に、ハイブリドーマは腹水癌化した。腹水のたまったマウスから腹水を採取し、2000rpmで5分間、4℃で遠心し、50%飽和硫酸アンモニウムにて塩析し、沈渣を溶かして10000gで10分間、4℃でした。プレフィルター、メンブランフィルター(0.22μm)を通過させた後、Protein G Sepharose (GEヘルスケア バイオサイエンス)を用いて精製した後、PBSで透析(3時間以上x4回)を行った。その結果得られた4種の抗LAT1/CD98モノクローナル抗体をLG9111モノクローナル抗体、LG9112モノクローナル抗体、LG9113モノクローナル抗体及びLG9114モノクローナル抗体とした。
腫瘍細胞株に対するモノクローナル抗体の結合性の検討
ヒト腫瘍細胞株4種を用いて抗LAT1/CD98モノクローナル抗体の結合性をFCM解析により測定した。ヒト腫瘍細胞株をPBSにて1×105cells/wellになるように調整し、50μLずつチューブに分注した。この細胞浮遊液に40μg/mLに調製した各モノクローナル抗体50μLを加え、4℃で45分反応させた。0.1%BSA-PBS100μLを加え、500gで3分間、4℃で遠心する洗浄を3回行い、細胞ペレットに200倍希釈したPE-labeled anti Rat IgG(Jackson Immuno Research)を50μL加え、遮光状態で4℃で45分間反応させた。0.1%BSA-PBS100μLを加え、500gで3分間、4℃で遠心する洗浄を3回行い、PBS500μLに懸濁し、FCMチューブに移した。死細胞を除くため測定直前にPI100μLを添加し、FACSCalibur(Becton Dickinson)にて測定した。図1に示すように、取得した4種のモノクローナル抗体は種々の癌細胞株に対して結合活性を示し、特に大腸癌細胞株HCT116に対してより高い結合活性が認められた。また、LGtra01-01モノクローナル抗体(特開2011-24537に開示された抗体)に比べて、10倍以上高い結合活性が認められた。
ヒトキメラ抗体の作製
樹立した抗LAT1/CD98抗体産生ハイブリドーマ株からtotal RNAを分離し、SMARTerTM RACE cDNA. Amplification Kit (クロンテック)を使ってcDNAを合成した。得られたcDNAよりpolymerase chain reaction(PCR)法により重鎖および軽鎖可変領域をコードするcDNAを増幅し、クローニングベクターにサブクローニングした。得られた cDNAの塩基配列を解析し、常法(<http://www.bioinf.org.uk/abs/>に記載)により各抗体の重鎖及び軽鎖の可変領域のアミノ酸配列(配列番号31~38)及びComplementarity determining region(CDR)のアミノ酸配列(配列番号7~30)を決定した。CDR配列特異的プライマーを合成し、それを用いて、抽出したプラスミドDNAからCDRを増幅し、ヒトキメラ抗体重鎖発現ベクターもしくはヒトキメラ抗体軽鎖発現ベクターに組み込んだ。得られたプラスミドはLigaseを用いて結合し、ヒトキメラ抗体産生プラスミドを作製した。FreeStyleTM MAX Reagent (インビトロジェン)を用いて、ヒトキメラ抗体産生プラスミドをFreeStyle 293F細胞 (インビトロジェン)に遺伝子導入し、96時間 旋回培養 (FreeStyleTM 293培地, 37℃, 8%CO2, 135rpm)後の培養上清を取得した。培養上清はProtein G Sepharose (GEヘルスケア バイオサイエンス)を用いて精製した後、PBSで透析(3時間以上x4回)を行い、ヒトキメラLAT1/CD98抗体を取得した。
ヒトキメラ抗体による抗体依存性細胞障害活性の検討
ヒトより血液をヘパリン採血管(テルモ VP-H100K)に採取した。PBSを加え2倍に希釈し、希釈したヘパリン血18mLをリンフォセパール I(IBL 23010)12mLに対し静かに重層した。400gで30分間遠心後、上層の血漿層を静かに除去し、中間層の単核球画分を分取した。PBSを加え2倍に希釈し、200gで10分間遠心し、上清を除去した。PBS10mLを加え、200gで10分間遠心する洗浄を2回行い、5%FBS-RPMI1640 に懸濁した細胞をエフェクター細胞懸濁液とした。一方、標的細胞としてヒト腫瘍細胞を2×105cells/mLとなるように5%FBS-RPMI1640で懸濁し、U底96well plateに1x104cells/wellになるように50μLずつ分注した。ヒトキメラ抗体50μL加え、4℃で15分間インキュベート後、遠心し上清を捨てた。エフェクター細胞懸濁液100μLを加え(同時にコントロールとして、エフェクター細胞のみのwell(Effector Spontaneous)、標的細胞のみのwell(Target Spontaneous)を作製)、37℃、5%CO2で4時間インキュベート(同時にコントロールとして、終了の45分前に標的細胞に10xLysis bufferを加えたwell(Terget Max)を作製)した。インキュベート後、軽くシェイクし、200gで5分間遠心し、上清50μLを平底96well plateに移した。Cytotox96 Non―Radioactive cytotoxicity assay(Promega G1780)を用い、キットに添付のプロトコールに従って反応させ、プレートリーダー(TECAN Infinite M200)を用いて490nm蛍光波長を測定し、次の式で細胞障害率を算出した。細胞障害率(%)=(Experimental - Effector Spontaneous - Target Spontaneous)/(Target Max - Target Spontaneous)×100。図2に示すようにLG9111ヒトキメラ抗体及びLG9113ヒトキメラ抗体において、抗体濃度依存的なADCC活性が検出され、ヒト大腸癌細胞株(HCT116)に対し抗体濃度20μg/mLでそれぞれ79%、46%の細胞障害率が認められた。また、ヒト肺癌細胞株(NCI-H1944)に対し35%以上の細胞障害率が認められた。
モノクローナル抗体のインターナリゼーション活性の検討
ヒト腫瘍細胞株を用いて抗LAT1/CD98モノクローナル抗体のインターナリゼーション活性をFCM解析により測定した。ヒト大腸癌細胞株HCT116を0.1%BSA-PBSで懸濁し、U底96well plateに1x105cells/wellになるように50μLずつ分注した。この細胞浮遊液に20μg/mLに調製した各モノクローナル抗体50μLを加え、4℃で45分反応させた。0.1%BSA-PBS150μLを加え、500gで3分間、4℃で遠心する洗浄を3回行い、モノクローナル抗体を結合させた細胞ペレットを得た。この細胞ペレットに0.1%BSA-PBS100μLを加え、37℃(インターナリゼーションが誘導される温度)または4℃(インターナリゼーションが誘導されない温度)で、それぞれ1時間インキュベートした。0.1%BSA-PBS150μLを加え、500gで3分間、4℃で遠心する洗浄を3回行った。200倍希釈したPE-labeled anti Rat IgG(Jackson Immuno Research)を50μL加え、遮光状態で4℃で30分間反応させた。0.1%BSA-PBS150μLを加え、500gで3分間、4℃で遠心する洗浄を3回行い、PBS500μLに懸濁し、FCMチューブに移した。死細胞を除くため測定直前にPI100μLを添加し、FACSCalibur(Becton Dickinson)にて測定した。図3(A)に示すように、4℃でインキュベートした場合に比べ、37℃でインキュベートした場合においてモノクローナル抗体の結合による蛍光強度の減少が認められた。
配列番号:8 LG9111軽鎖相補性決定領域2(CDRL2)
配列番号:9 LG9111軽鎖相補性決定領域3(CDRL3)
配列番号:10 LG9111重鎖相補性決定領域1(CDRH1)
配列番号:11 LG9111重鎖相補性決定領域2(CDRH2)
配列番号:12 LG9111重鎖相補性決定領域3(CDRH3)
配列番号:13 LG9112軽鎖相補性決定領域1(CDRL1)
配列番号:14 LG9112軽鎖相補性決定領域2(CDRL2)
配列番号:15 LG9112軽鎖相補性決定領域3(CDRL3)
配列番号:16 LG9112重鎖相補性決定領域1(CDRH1)
配列番号:17 LG9112重鎖相補性決定領域2(CDRH2)
配列番号:18 LG9112重鎖相補性決定領域3(CDRH3)
配列番号:19 LG9113軽鎖相補性決定領域1(CDRL1)
配列番号:20 LG9113軽鎖相補性決定領域2(CDRL2)
配列番号:21 LG9113軽鎖相補性決定領域3(CDRL3)
配列番号:22 LG9113重鎖相補性決定領域1(CDRH1)
配列番号:23 LG9113重鎖相補性決定領域2(CDRH2)
配列番号:24 LG9113重鎖相補性決定領域3(CDRH3)
配列番号:25 LG9114軽鎖相補性決定領域1(CDRL1)
配列番号:26 LG9114軽鎖相補性決定領域2(CDRL2)
配列番号:27 LG9114軽鎖相補性決定領域3(CDRL3)
配列番号:28 LG9114重鎖相補性決定領域1(CDRH1)
配列番号:29 LG9114重鎖相補性決定領域2(CDRH2)
配列番号:30 LG9114重鎖相補性決定領域3(CDRH3)
配列番号:31 LG9111軽鎖可変領域
配列番号:32 LG9111重鎖可変領域
配列番号:33 LG9112軽鎖可変領域
配列番号:34 LG9112重鎖可変領域
配列番号:35 LG9113軽鎖可変領域
配列番号:36 LG9113重鎖可変領域
配列番号:37 LG9114軽鎖可変領域
配列番号:38 LG9114重鎖可変領域
Claims (29)
- LAT1/CD98を発現する細胞のLAT1/CD98複合体の細胞外領域に特異的に結合する抗体またはその抗原結合断片であって、
(1)軽鎖相補性決定領域1(CDRL1)、軽鎖相補性決定領域2(CDRL2)、および軽鎖相補性決定領域3(CDRL3)として、それぞれ、配列番号7、配列番号8、および配列番号9のアミノ酸配列、または配列番号7、配列番号8、および配列番号9のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含み、
重鎖相補性決定領域1(CDRH1)、重鎖相補性決定領域2(CDRH2)、および重鎖相補性決定領域3(CDRH3)として、それぞれ、配列番号10、配列番号11、および配列番号12のアミノ酸配列、もしくは配列番号10、配列番号11、および配列番号12のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含む、抗体またはその抗原結合断片、
(2)CDRL1、CDRL2、およびCDRL3として、それぞれ、配列番号13、配列番号14、および配列番号15のアミノ酸配列、もしくは配列番号13、配列番号14、および配列番号15のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含み、
CDRH1、CDRH2、およびCDRH3として、それぞれ、配列番号16、配列番号17、配列番号18のアミノ酸配列、もしくは配列番号16、配列番号17、および配列番号18のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含む、抗体またはその抗原結合断片、
(3)CDRL1、CDRL2、およびCDRL3として、それぞれ、配列番号19、配列番号20、および配列番号21、もしくは配列番号19、配列番号20、および配列番号21のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含み、
CDRH1、CDRH2、およびCDRH3として、それぞれ、配列番号22、配列番号23、および配列番号24のアミノ酸配列、もしくは配列番号22、配列番号23、および配列番号24のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異を有する各アミノ酸配列を含む、抗体またはその抗原結合断片、または
(4)CDRL1、CDRL2、およびCDRL3として、それぞれ、配列番号25、配列番号26、および配列番号27のアミノ酸配列、もしくは配列番号25、配列番号26、および配列番号27のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含み、
CDRH1、CDRH2、およびCDRH3として、それぞれ、配列番号28、配列番号29、および配列番号30のアミノ酸配列、もしくは配列番号28、配列番号29、および配列番号30のアミノ酸配列に1個もしくは数個のアミノ酸残基の変異をそれぞれ有するアミノ酸配列を含む、抗体またはその抗原結合断片。 - LAT1/CD98を発現する細胞のLAT1/CD98複合体の細胞外領域に特異的に結合する抗体またはその抗原結合断片であって、
(1)X1ASQX2VGNNVA(配列番号1)のアミノ酸配列を含む軽鎖相補性決定領域1(CDRL1)、
(2)YASX3RX4T(配列番号2)のアミノ酸配列を含む軽鎖相補性決定領域2(CDRL2)、
(3)QRX5YKSPYT(配列番号3)のアミノ酸配列を含む軽鎖相補性決定領域3(CDRL3)、
(4)GFSLPTSSVS(配列番号4)のアミノ酸配列を含む重鎖相補性決定領域1(CDRH1)、
(5)VIWSNGNTDYSSX6X7KS(配列番号5)のアミノ酸配列を含む重鎖相補性決定領域2(CDRH2)、および
(6)NFRNX8PGVMDA(配列番号6)のアミノ酸配列を含む重鎖相補性決定領域3(CDRH3)
(但し、X1~X8は、任意の天然に存在するアミノ酸残基である)
を含む、抗体またはその抗原結合断片。 - X1が、RまたはKであり、
X2が、NまたはTであり、
X3が、SまたはNであり、
X4が、HまたはNであり、
X5が、VまたはIであり、
X6が、AまたはRであり、
X7が、IまたはFである、
X8が、DまたはNである、請求項2に記載の抗体またはその抗原結合断片。 - (1)X1がR、X2がN、X3がN、X4がN、X5がI、X6がA、X7がI、X8がDであるか、
(2)X1がK、X2がN、X3がS、X4がH、X5がV、X6がR、X7がF、X8がDであるか、
(3)X1がK、X2がT、X3がS、X4がH、X5がV、X6がR、X7がF、X8がDであるか、または
(4)X1がK、X2がN、X3がS、X4がH、X5がV、X6がR、X7がI、X8がNである、請求項2に記載の抗体またはその抗原結合断片。 - 請求項1~4のいずれか一項に記載の抗体またはその抗原結合断片であって、
(1)配列番号31のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む軽鎖可変領域(LH)、および
配列番号31のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む重鎖可変領域(VL)、
(2)配列番号33のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む軽鎖可変領域(LH)、および
配列番号34のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む重鎖可変領域(VL)、
(3)配列番号35のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む軽鎖可変領域(LH)、および
配列番号36のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む重鎖可変領域(VL)、または
(4)配列番号37のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む軽鎖可変領域(LH)、および
配列番号38のアミノ酸配列と90%以上の同一性を有するアミノ酸配列を含む重鎖可変領域(VL)、
を含有する、抗体もしくはその抗原結合断片。 - 請求項1~5のいずれか一項に記載の抗体もしくはその抗原結合断片であって、
(1)配列番号31のアミノ酸配列を含む軽鎖可変領域(VL)、および
配列番号32のアミノ酸配列を含む重鎖可変領域(VH)、
(2)配列番号33のアミノ酸配列を含む軽鎖可変領域(VL)、および
配列番号34のアミノ酸配列を含む重鎖可変領域(VH)、
(3)配列番号35のアミノ酸配列を含む軽鎖可変領域(VL)、および
配列番号36のアミノ酸配列を含む重鎖可変領域(VH)、または
(4)配列番号37のアミノ酸配列を含む軽鎖可変領域(VL)、および
配列番号38のアミノ酸配列を含む重鎖可変領域(VH)、
を含有する、抗体もしくはその抗原結合断片。 - LAT1/CD98を発現する細胞に対する細胞障害活性および/またはインターナリゼーション活性を有する、請求項1~6のいずれか一項に記載の抗体またはその抗原結合断片。
- サブクラスがIgGである、請求項1~7のいずれか一項に記載の抗体またはその抗原結合断片。
- 前記IgGが、IgG2aまたはIgG1である、請求項8に記載の抗体またはその抗原結合断片。
- 前記抗原結合断片が、Fab、Fab’、F(ab’)2、scFv、dsFv、ds-scFv、それらのダイマー、ミニボディ(minobodies)、ダイアボディ(diabodies)、およびマルチマー、または二重特異性抗体断片である、請求項1~9のいずれか一項に記載の抗体またはその抗原結合断片。
- モノクローナル抗体である、請求項1~10のいずれか一項に記載の抗体またはその抗原結合断片。
- ラット、マウス、霊長類、またはヒト抗体である、請求項1~11のいずれか一項に記載の抗体またはその抗原結合断片。
- キメラ抗体またはヒト化抗体である、請求項1~11のいずれか一項に記載の抗体またはその抗原結合断片。
- 請求項1~13のいずれか一項に記載の抗体またはその抗原結合断片と少なくとも1つの細胞毒性薬、抗腫瘍剤または放射性同位体を含んでなるイムノコンジュゲート。
- 請求項1~14のいずれか一項に記載の抗体またはその抗原結合断片をコードする単離された核酸分子。
- 請求項15に記載の核酸分子を含む発現ベクター。
- 請求項15に記載の核酸分子を含むかまたは該核酸分子を導入した、請求項1~13のいずれか一項に記載の抗体を産生する、ハイブリドーマ細胞または遺伝子導入細胞。
- 請求項17に記載の細胞を培養し、得られる培養物からLAT1/CD98複合体に特異的に結合する抗体を採取することを含む、LAT1/CD98複合体の細胞外領域に特異的に結合するモノクローナル抗体の製造方法。
- 請求項17に記載の細胞から抗LAT1/CD98モノクローナル抗体をコードする遺伝子を単離し、該遺伝子を含む発現ベクターを構築し、該発現ベクターを宿主に導入して前記モノクローナル抗体を発現せしめ、得られる宿主、宿主の培養上清または宿主の分泌物からLAT1/CD98の細胞外領域に特異的に結合するモノクローナル抗体を採取することを含む、LAT1/CD98の細胞外領域に特異的に結合するモノクローナル抗体の製造方法。
- 前記宿主が、大腸菌、酵母細胞、昆虫細胞、哺乳動物細胞、植物細胞、または哺乳動物である、請求項19に記載の製造方法。
- 請求項1~14のいずれか一項に記載の抗体またはその抗原結合断片またはイムノコンジュゲートを含有する組成物であって、LAT1/CD98を発現する細胞に適用して該細胞のアポトーシスを誘導するために使用する、組成物。
- 請求項1~14のいずれか一項に記載の抗体またはその抗原結合断片またはイムノコンジュゲートを含有する、腫瘍の予防または治療のための医薬。
- 請求項1~14のいずれか一項に記載の抗体またはその抗原結合断片またはイムノコンジュゲートを含有する組成物であって、LAT1/CD98を発現する細胞を検出するために使用する、組成物。
- 請求項23の組成物と、生体から採取された試料とを反応させ、反応したシグナルを検出することを特徴とする、腫瘍の検出方法。
- 請求項23の組成物を癌細胞と接触する工程を含む試験管内の腫瘍の免疫検出方法。
- 請求項23の組成物を個体に投与する工程および近赤外光イメージング、PET、MRIまたは超音波イメージングによって得られる検出映像を得る工程を含む生体内で腫瘍の映像化方法。
- 請求項1~14のいずれか一項に記載の抗体またはその抗原結合断片またはイムノコンジュゲートを含有する、腫瘍の診断のための医薬。
- 前記腫瘍が、大腸癌、結腸直腸癌、肺癌、乳癌、脳腫瘍、黒色腫、腎細胞癌、膀胱癌、白血病、リンパ腫、T細胞リンパ腫、多発性骨髄腫、胃癌、膵臓癌、子宮頸癌、子宮内膜癌、卵巣癌、食道癌、肝臓癌、頭頸部扁平上皮癌、皮膚癌、尿路癌、前立腺癌、絨毛癌、咽頭癌、喉頭癌、舌癌、口腔癌、胆嚢癌、甲状腺癌、中皮腫、胸膜腫、男性胚腫、子宮内膜過形成、子宮内膜症、胚芽腫、線維肉腫、カポジ肉腫、血管腫、海綿状血管腫、血管芽腫、網膜芽腫、星状細胞腫、神経線維腫、稀突起謬腫、髄芽腫、神経芽腫、神経膠腫、横紋筋肉腫、謬芽腫、骨原性肉腫、平滑筋肉腫、甲状肉腫、およびウィルムス腫瘍からなる群から選択される少なくとも1つである、請求項22または請求項27に記載の医薬。
- 以下の(1)~(6)からなる群から選択される相補性決定領域(CDR):
(1)配列番号7、13、19、または25のアミノ酸配列を含む軽鎖相補性決定領域1(CDRL1)、
(2)配列番号8、14、20、または26のアミノ酸配列を含む軽鎖相補性決定領域2(CDRL2)、
(3)配列番号9、15、21、または27のアミノ酸配列を含む軽鎖相補性決定領域3(CDRL3)、
(4)配列番号10、16、22、または28のアミノ酸配列を含む重鎖相補性決定領域1(CDRH1)、
(5)配列番号11、17、23、または29のアミノ酸配列を含む重鎖相補性決定領域2(CDRH2)、および
(6)配列番号12、18、24、または30のアミノ酸配列を含む重鎖相補性決定領域3(CDRH3)。
Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201380040758.1A CN104662153A (zh) | 2012-06-08 | 2013-06-10 | 针对转运体的抗体及其用途 |
EP13799754.0A EP2878670B1 (en) | 2012-06-08 | 2013-06-10 | Antibody against transporter and use thereof |
IN1MUN2015 IN2015MN00001A (ja) | 2012-06-08 | 2013-06-10 | |
JP2014520078A JP6421371B2 (ja) | 2012-06-08 | 2013-06-10 | トランスポーターに対する抗体およびその用途 |
AU2013272504A AU2013272504A1 (en) | 2012-06-08 | 2013-06-10 | Antibody against transporter and use thereof |
CA2875451A CA2875451A1 (en) | 2012-06-08 | 2013-06-10 | Antibody against transporter and use thereof |
KR1020157000166A KR20150013935A (ko) | 2012-06-08 | 2013-06-10 | 트랜스포터에 대한 항체 및 이의 용도 |
US14/561,944 US9725519B2 (en) | 2012-06-08 | 2014-12-05 | Antibody against transporter and use thereof |
HK15108643.7A HK1208053A1 (en) | 2012-06-08 | 2015-09-04 | Antibody against transporter and use thereof |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2012131424 | 2012-06-08 | ||
JP2012-131424 | 2012-06-08 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US14/561,944 Continuation-In-Part US9725519B2 (en) | 2012-06-08 | 2014-12-05 | Antibody against transporter and use thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2013183786A1 true WO2013183786A1 (ja) | 2013-12-12 |
Family
ID=49712170
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2013/065996 WO2013183786A1 (ja) | 2012-06-08 | 2013-06-10 | トランスポーターに対する抗体およびその用途 |
Country Status (10)
Country | Link |
---|---|
US (1) | US9725519B2 (ja) |
EP (1) | EP2878670B1 (ja) |
JP (1) | JP6421371B2 (ja) |
KR (1) | KR20150013935A (ja) |
CN (1) | CN104662153A (ja) |
AU (1) | AU2013272504A1 (ja) |
CA (1) | CA2875451A1 (ja) |
HK (1) | HK1208053A1 (ja) |
IN (1) | IN2015MN00001A (ja) |
WO (1) | WO2013183786A1 (ja) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015173970A1 (ja) * | 2014-05-15 | 2015-11-19 | ジェイファーマ株式会社 | 抗悪性腫瘍剤組成物 |
US10948493B2 (en) | 2015-04-17 | 2021-03-16 | Ventana Medical Systems, Inc. | Antibodies, compositions, and immunohistochemistry methods for detecting C4.4a |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2018219226A1 (en) | 2017-02-07 | 2019-08-15 | Seattle Children's Hospital (dba Seattle Children's Research Institute) | Phospholipid ether (PLE) CAR T cell tumor targeting (CTCT) agents |
WO2018160622A1 (en) | 2017-02-28 | 2018-09-07 | Endocyte, Inc. | Compositions and methods for car t cell therapy |
WO2018195339A1 (en) | 2017-04-19 | 2018-10-25 | Board Of Regents, The University Of Texas System | Immune cells expressing engineered antigen receptors |
US11779602B2 (en) | 2018-01-22 | 2023-10-10 | Endocyte, Inc. | Methods of use for CAR T cells |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4816567A (en) | 1983-04-08 | 1989-03-28 | Genentech, Inc. | Recombinant immunoglobin preparations |
WO1994029348A2 (en) | 1993-06-03 | 1994-12-22 | Therapeutic Antibodies Inc. | Production of antibody fragments |
WO2007114496A1 (ja) * | 2006-04-06 | 2007-10-11 | Kirin Pharma Kabushiki Kaisha | 新規抗cd98抗体 |
JP2011024537A (ja) | 2009-07-29 | 2011-02-10 | Kinki Univ | トランスポーターに対する抗体およびその用途 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK2403528T3 (en) * | 2009-03-02 | 2016-05-23 | Aduro Biotech Holdings Europ B V | ANTIBODIES AGAINST A proliferation-inducing ligand (April) |
WO2011017294A1 (en) * | 2009-08-07 | 2011-02-10 | Schering Corporation | Human anti-rankl antibodies |
-
2013
- 2013-06-10 CA CA2875451A patent/CA2875451A1/en not_active Abandoned
- 2013-06-10 EP EP13799754.0A patent/EP2878670B1/en active Active
- 2013-06-10 JP JP2014520078A patent/JP6421371B2/ja active Active
- 2013-06-10 AU AU2013272504A patent/AU2013272504A1/en not_active Abandoned
- 2013-06-10 KR KR1020157000166A patent/KR20150013935A/ko not_active Application Discontinuation
- 2013-06-10 CN CN201380040758.1A patent/CN104662153A/zh active Pending
- 2013-06-10 WO PCT/JP2013/065996 patent/WO2013183786A1/ja active Application Filing
- 2013-06-10 IN IN1MUN2015 patent/IN2015MN00001A/en unknown
-
2014
- 2014-12-05 US US14/561,944 patent/US9725519B2/en active Active
-
2015
- 2015-09-04 HK HK15108643.7A patent/HK1208053A1/xx unknown
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4816567A (en) | 1983-04-08 | 1989-03-28 | Genentech, Inc. | Recombinant immunoglobin preparations |
WO1994029348A2 (en) | 1993-06-03 | 1994-12-22 | Therapeutic Antibodies Inc. | Production of antibody fragments |
WO2007114496A1 (ja) * | 2006-04-06 | 2007-10-11 | Kirin Pharma Kabushiki Kaisha | 新規抗cd98抗体 |
JP2011024537A (ja) | 2009-07-29 | 2011-02-10 | Kinki Univ | トランスポーターに対する抗体およびその用途 |
Non-Patent Citations (45)
Title |
---|
"Current Topics in Microbiology and Immunology-1", EUROPEAN J. IMMUNOLOGY, vol. 6, 1976, pages 511 - 519 |
ADAMS ET AL., CAN.RES, vol. 53, 1993, pages 4026 - 4034 |
ALT ET AL., FEBS LETT, vol. 454, 1999, pages 90 - 94 |
BIRD ET AL., SCIENCE, vol. 242, 1988, pages 423 - 426 |
CLACKSON ET AL., NATURE, vol. 352, 1991, pages 624 - 628 |
COLOMA ET AL., NATURE BIOTECHNOL., vol. 15, 1997, pages 159 - 163 |
GLOCKSHUBER ET AL., BIOCHEMISTRY, vol. 29, 1990, pages 1362 - 1367 |
HAYNES ET AL., J IMMUNOL., vol. 126, no. 4, April 1981 (1981-04-01), pages 1409 - 14 |
HOLLIGER ET AL., PNAS, vol. 90, 1993, pages 6444 - 6448 |
HU ET AL., CANCER RES., vol. 56, 1996, pages 3055 - 3061 |
HUSTON ET AL., INT. REV. IMMUNOL, vol. 10, 1993, pages 195 - 217 |
HUSTON ET AL., PNAS, vol. 85, pages 5879 - 5883 |
J MOL BIOL, vol. 215, 1990, pages 403 |
J. IMMUNOLOGY, vol. 123, 1979, pages 1548 - 1550 |
KAIRA ET AL., CANCER SCI., vol. 100, no. 2, 2009, pages 249 - 254 |
KAIRA ET AL., CANCER SCI., vol. 99, no. 12, 2008, pages 2380 - 2386 |
KARLIN; ALTSCHUL, PNAS, vol. 87, 1990, pages 2264 |
KIPRIYANOV ET AL., CELL. BIOPHYS, vol. 26, 1995, pages 187 - 204 |
KIPRIYANOV ET AL., INT. J. CAN, vol. 77, 1998, pages 763 - 772 |
KIPRIYANOV ET AL., J. MOL. BIOL., vol. 293, 1999, pages 41 - 56 |
KOHLER ET AL., NATURE, vol. 256, 1975, pages 495 |
KONTERMANN ET AL., J. IMMUNOL. METHODS, vol. 226, 1999, pages 179 - 188 |
KORTT ET AL., PROTEIN ENG, vol. 10, 1997, pages 423 - 433 |
KOSTELNY ET AL., J. IMMUNOL., vol. 148, 1992, pages 1547 - 1553 |
KURUCZ ET AL., J. IMMOL., vol. 154, 1995, pages 4576 - 4582 |
LE GALL ET AL., FEBS LETT, vol. 453, 1999, pages 164 - 168 |
MARKS ET AL., J. MOL. BIOL., vol. 222, 1991, pages 581 - 597 |
MASUKO ET AL., JPN J CANCER RES., vol. 76, no. 5, May 1985 (1985-05-01), pages 386 - 94 |
MCCARTNEY ET AL., PROTEIN ENG., vol. 8, 1995, pages 301 - 314 |
MORRISON ET AL., PROC. NATL. ACAD. SCI. USA, vol. 81, 1984, pages 6851 - 6855 |
MORRISON ET AL., PROC. NATL. ACAD. SCI., USA, vol. 81, 1984, pages 6851 |
MULLER ET AL., FEBS LETT, vol. 432, 1998, pages 45 - 49 |
NATURE, vol. 256, 1975, pages 495 - 497 |
NATURE, vol. 276, 1978, pages 269 - 270 |
OHKAWA,M. ET AL.: "Oncogenicity of L-type amino- acid transporter 1 (LAT1) revealed by targeted gene disruption in chicken DT40 cells: LAT1 is a promising molecular target for human cancer therapy.", BIOCHEM.BIOPHYS.RES.COMMUN., vol. 406, 2011, pages 649 - 655, XP028370698 * |
OHNO ET AL., CANCER SCI., vol. 99, no. 5, 2008, pages 1000 - 1007 |
OHNO,Y. ET AL.: "Production and characterization of highly tumor-specific rat monoclonal antibodies recognizing the extracellular domain of human L-type amino-acid transporter 1.", CANCER SCI., vol. 99, no. 5, 2008, pages 1000 - 1007, XP028370698 * |
PACK ET AL., BIOCHEMISTRY, vol. 31, 1992, pages 1579 - 1584 |
PNAS, vol. 90, 1993, pages 5873 |
See also references of EP2878670A4 |
SHALABY ET AL., J. EXP. MED., vol. 175, 1992, pages 217 - 225 |
WHITLOW ET AL., METHODS COMPANION METHODS ENZYMOL, vol. 2, 1991, pages 97 - 105 |
YANAGIDA ET AL., BIOCHIMICA ET BIOPHYSICA ACTA, vol. 1514, 2001, pages 291 - 302 |
YOSHIKATSU KANAI, PROTEIN, NUCLEIC ACID AND ENZYME, vol. 46, no. 5, 2001, pages 629 - 637 |
ZHU ET AL., PROTEIN SCI., vol. 6, 1997, pages 781 - 788 |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015173970A1 (ja) * | 2014-05-15 | 2015-11-19 | ジェイファーマ株式会社 | 抗悪性腫瘍剤組成物 |
CN105392498A (zh) * | 2014-05-15 | 2016-03-09 | J制药股份有限公司 | 抗恶性肿瘤剂组合物 |
US10172835B2 (en) | 2014-05-15 | 2019-01-08 | J-Pharma Co., Ltd. | Anticancer agent composition |
US10948493B2 (en) | 2015-04-17 | 2021-03-16 | Ventana Medical Systems, Inc. | Antibodies, compositions, and immunohistochemistry methods for detecting C4.4a |
US11719699B2 (en) | 2015-04-17 | 2023-08-08 | Ventana Medical Systems, Inc. | Antibodies, compositions, and immunohistochemistry methods for detecting C4.4a |
Also Published As
Publication number | Publication date |
---|---|
JPWO2013183786A1 (ja) | 2016-02-01 |
JP6421371B2 (ja) | 2018-11-14 |
EP2878670B1 (en) | 2019-08-07 |
EP2878670A4 (en) | 2016-03-02 |
EP2878670A1 (en) | 2015-06-03 |
CA2875451A1 (en) | 2013-12-12 |
US20150147278A1 (en) | 2015-05-28 |
CN104662153A (zh) | 2015-05-27 |
KR20150013935A (ko) | 2015-02-05 |
HK1208053A1 (en) | 2016-02-19 |
IN2015MN00001A (ja) | 2015-10-16 |
AU2013272504A1 (en) | 2015-01-22 |
US9725519B2 (en) | 2017-08-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US11161904B2 (en) | Anti-PD-1 antibody and use thereof | |
TWI767899B (zh) | Psma及cd3雙特異性t細胞嚙合抗體構築體 | |
JP7080213B2 (ja) | 新規抗pd-l1抗体 | |
CN108271376B (zh) | 结合dll3和cd3的双特异性抗体构建体 | |
WO2019238012A1 (zh) | 可以阻断CD47和SIRPa相互作用的抗体及其应用 | |
CN109476734B (zh) | Cd70和cd3的抗体构建体 | |
JP6392770B2 (ja) | 抗cd47抗体およびその使用方法 | |
JP2020122013A (ja) | Cd3イプシロンおよびbcmaに対する二特異性抗体 | |
WO2021027674A1 (zh) | 一种含有抗体的肿瘤治疗剂的开发和应用 | |
CN112512581A (zh) | 针对cldn18.2和cd3的抗体构建体 | |
US11639388B2 (en) | CD3 antigen binding fragment and application thereof | |
JP6421371B2 (ja) | トランスポーターに対する抗体およびその用途 | |
JP2022506719A (ja) | タウ認識抗体 | |
JP2024010066A (ja) | 抗cd3イプシロン抗体およびそれを使用する方法 | |
WO2015076425A1 (ja) | 新規モノクローナル抗体 | |
US20230272067A1 (en) | Human monoclonal antibodies against tigit for immune related diseases | |
WO2011007853A1 (ja) | 癌特異的アイソフォームに対するモノクローナル抗体 | |
EP4058485A1 (en) | Method for reduced aggregate formation in downstream processing of bispecific antigen-binding molecules | |
WO2019174637A1 (zh) | 一种针对tim-3的全人源化抗体分子、抗原结合片段及其医药用途 | |
JP2011024537A (ja) | トランスポーターに対する抗体およびその用途 | |
JP2011050355A (ja) | トランスポーターに対する抗体およびその用途 | |
CN113164601B (zh) | 一种分离的抗原结合蛋白及其用途 | |
CN113166264B (zh) | 一种分离的抗原结合蛋白及其用途 | |
WO2023241656A1 (zh) | 包含抗cldn18.2抗体的双特异性抗体、药物组合物及用途 | |
US20220380446A1 (en) | Antibodies for treating alpha-synucleinopathies |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 13799754 Country of ref document: EP Kind code of ref document: A1 |
|
ENP | Entry into the national phase |
Ref document number: 2014520078 Country of ref document: JP Kind code of ref document: A |
|
ENP | Entry into the national phase |
Ref document number: 2875451 Country of ref document: CA |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: P1352/2014 Country of ref document: AE |
|
ENP | Entry into the national phase |
Ref document number: 20157000166 Country of ref document: KR Kind code of ref document: A |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2013799754 Country of ref document: EP |
|
ENP | Entry into the national phase |
Ref document number: 2013272504 Country of ref document: AU Date of ref document: 20130610 Kind code of ref document: A |