HRP20202019T1 - Novi peptidi i kombinacija peptida za uporabu u imunoterapiji protiv raka jajnika i drugih malignih tumora - Google Patents

Novi peptidi i kombinacija peptida za uporabu u imunoterapiji protiv raka jajnika i drugih malignih tumora Download PDF

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HRP20202019T1
HRP20202019T1 HRP20202019TT HRP20202019T HRP20202019T1 HR P20202019 T1 HRP20202019 T1 HR P20202019T1 HR P20202019T T HRP20202019T T HR P20202019TT HR P20202019 T HRP20202019 T HR P20202019T HR P20202019 T1 HRP20202019 T1 HR P20202019T1
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Croatia
Prior art keywords
cancer
peptide
cell
nucleic acid
antibody
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HRP20202019TT
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English (en)
Inventor
Andrea Mahr
Toni Weinschenk
Helen HÖRZER
Oliver Schoor
Jens Fritsche
Harpreet Singh
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Immatics Biotechnologies Gmbh
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Priority claimed from GBGB1511546.2A external-priority patent/GB201511546D0/en
Application filed by Immatics Biotechnologies Gmbh filed Critical Immatics Biotechnologies Gmbh
Publication of HRP20202019T1 publication Critical patent/HRP20202019T1/hr

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Claims (14)

1. Peptid koji sadrži aminokiselinsku sekvencu u skladu sa ID BR. SEKV. 11; ili njegova farmaceutski prihvatljiva sol.
2. Peptid u skladu sa patentnim zahtjevom 1, naznačen time što navedeni peptid sadrži nepeptidne veze.
3. Peptid u skladu sa patentnim zahtjevom 1 ili 2, naznačen time što je navedeni peptid stopljen sa N-terminalnim aminokiselinama HLA-DR antigen-asociranog nepromjenljivog lanca (Ii).
4. T-stanični receptor, poželjno rekombinantni, topivi ili T- stanični receptor vezan za membranu koji je specifično reaktivan sa HLA ligandom, naznačen time što se navedeni ligand sastoji od aminokiselinske sekvence ID BR. SEKV. 11.
5. Antitijelo, konkretno topivo ili antitijelo vezano za membranu, koje specifično prepoznaje peptid u skladu sa bilo kojim od patentnih zahtjeva 1 ili 2 kada je vezan za MHC molekulu.
6. Nukleinska kiselina koja kodira peptid u skladu sa bilo kojim od patentnih zahtjeva 1 do 3 ili TCR u skladu sa patentnim zahtjevom 4 ili antitijelo u skladu sa patentnim zahtjevom 5, izborno povezana sa heterolognom promoterskom sekvencom, ili vektor ekspresije koji eksprimira navedenu nukleinsku kiselinu.
7. Rekombinantna stanica domaćin koja sadrži peptid u skladu sa patentnim zahtjevom 1 do 3, ili nukleinska kiselina ili vektor ekspresije u skladu sa patentnim zahtjevom 6, naznačeno time što je navedena stanica domaćin poželjno stanica koja prezentira antigen kao što je dendritična stanica ili naznačeno time što je stanica domaćin poželjno T stanica ili NK stanica.
8. Postupak za proizvodnju peptida u skladu sa bilo kojim od patentnih zahtjeva 1 do 3, ili za proizvodnju T staničnog receptora u skladu sa patentnim zahtjevom 4 ili antitijelo u skladu sa patentnim zahtjevom 5, pri čemu se postupak sastoji od kultiviranja stanice domaćina u skladu sa patentnim zahtjevom 7 koja prezentira peptid u skladu sa patentnim zahtjevom 1 do 3 ili eksprimira nukleinsku kiselinu ili vektor ekspresije u skladu sa patentnim zahtjevom 6 i izoliranja peptida ili TCR-a ili antitijela iz stanice domaćina ili njenog medija za kultivaciju.
9. In vitro postupak za proizvodnju aktiviranih T limfocita, pri čemu se postupak sastoji od dovođenja u kontakt in vitro T stanica sa ljudskim MHC molekulama klase I sa ubačenim antigenom eksprimiranim na površini prikladne stanice koja prezentira antigen ili umjetne konstrukcije koja imitira stanicu koja prezentira antigen u toku vremenskog perioda koji je dovoljan da se navedene T stanice aktiviraju na antigen-specifičan način, naznačeno time što je navedeni antigen peptid u skladu sa patentnim zahtjevom 1.
10. Aktivirani T limfocit, proizveden pomoću postupka u skladu sa patentnim zahtjevom 9, koji selektivno prepoznaje stanicu koja prezentira peptid koji sadrži aminokiselinsku sekvencu navedenu u patentnom zahtjevu 1.
11. Farmaceutski pripravak koji sadrži najmanje jedan aktivan sastojak izabran iz grupe koju čine peptid u skladu sa bilo kojim od patentnih zahtjeva 1 do 3, nukleinska kiselina ili vektor ekspresije u skladu sa patentnim zahtjevom 4, stanica u skladu sa patentnim zahtjevom 7, aktivirani T limfocit u skladu sa patentnim zahtjevom 10 ili antitijelo u skladu sa patentnim zahtjevom 5 ili T-stanični receptor u skladu sa patentnim zahtjevom 4, i farmaceutski prihvatljiv nosač, i izborno, dodatne farmaceutski prihvatljive pomoćne materije i/ili stabilizatore.
12. Peptid u skladu sa bilo kojim od patentnih zahtjeva 1 do 3, nukleinska kiselina ili vektor ekspresije u skladu sa patentnim zahtjevom 4, stanica u skladu sa patentnim zahtjevom 7, aktivirani T limfocit u skladu sa patentnim zahtjevom 10 ili antitijelo u skladu sa patentnim zahtjevom 5 ili T-stanični receptor u skladu sa patentnim zahtjevom 4 za uporabu u medicini, poželjno za uporabu u dijagnosticiranju i/ili liječenju raka, ili za uporabu u proizvodnji lijeka protiv raka.
13. Peptid u skladu sa bilo kojim patentnim zahtjevom 1 do 3, nukleinska kiselina ili vektor ekspresije u skladu sa patentnim zahtjevom 4, stanica u skladu sa patentnim zahtjevom 7, aktivirani T limfocit u skladu sa patentnim zahtjevom 10 ili antitijelo u skladu sa patentnim zahtjevom 5 ili T-stanični receptor u skladu sa patentnim zahtjevom 4 za uporabu za dijagnosticiranje i/ili liječenje raka ili za uporabu u proizvodnji lijeka protiv raka u skladu sa patentnim zahtjevom 13, naznačenog time što je navedeni rak izabran iz grupe koju čine rak jajnika, nesitnostanični rak pluća, sitnostanični rak pluća, rak bubrega, rak mozga, rak crijeva ili rektuma, rak želuca, rak jetre, rak gušteraće, rak prostate, leukemija, rak dojke, karcinom Merkelovih stanica, melanom, rak jednjaka, rak mokraćnog mjehura, rak materice, rak žučnog mjehura, rak žučnih puteva i drugi tumori koji pokazuju prekomjernu ekspresiju proteina iz kojeg je dobiven peptid u skladu sa ID BR. SEKV 11.
14. Komplet koji se sastoji od: a) posude koja sadrži farmaceutsku mješavinu koja sadrži peptid u skladu sa bilo kojim od patentnih zahtjeva 1 do 3, nukleinsku kiselinu ili vektor ekspresije u skladu sa patentnim zahtjevom 4, stanicu u skladu sa patentnim zahtjevom 7, aktivirani T limfocit u skladu sa patentnim zahtjevom 10 ili antitijelo u skladu sa patentnim zahtjevom 5 ili T-stanični receptor u skladu sa patentnim zahtjevom 4, u otopini ili u liofiliziranom obliku; b) izborno, druge posude koja sadrži razrjeđivač ili otopinu za rekonstituciju za liofiliziranu formulaciju; c) izborno, najmanje još jedan peptid odabran iz grupe koja se sastoji od ID BR. SEKV 1 do 10 i 12 do 640, i d) izborno, upute za (i) uporabu otopine ili (ii) rekonstituciju i/ili uporabu liofilizirane formulacije, i e) izborno dalje sadrži jedan ili više od (iii) pufer, (iv) razrjeđivač, (v) filter, (vi) igla ili (v) brizgalica.
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