HRP20210698T1 - Peptidi i kombinacija peptida za uporabu u imunoterapiji protiv karcinoma dojke i drugih karcinoma - Google Patents

Peptidi i kombinacija peptida za uporabu u imunoterapiji protiv karcinoma dojke i drugih karcinoma Download PDF

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HRP20210698T1
HRP20210698T1 HRP20210698TT HRP20210698T HRP20210698T1 HR P20210698 T1 HRP20210698 T1 HR P20210698T1 HR P20210698T T HRP20210698T T HR P20210698TT HR P20210698 T HRP20210698 T HR P20210698T HR P20210698 T1 HRP20210698 T1 HR P20210698T1
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cancer
peptide
cell
antibody
nucleic acid
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Andrea Mahr
Toni Weinschenk
Helen HÖRZER
Oliver Schoor
Jens Fritsche
Harpreet Singh
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Immatics Biotechnologies Gmbh
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    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
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    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
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    • C07K14/4701Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
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    • C07K14/705Receptors; Cell surface antigens; Cell surface determinants
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    • C07K14/705Receptors; Cell surface antigens; Cell surface determinants
    • C07K14/72Receptors; Cell surface antigens; Cell surface determinants for hormones
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    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
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    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2803Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
    • C07K16/2833Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily against MHC-molecules, e.g. HLA-molecules
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    • C07K7/00Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
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    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/11DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/115Aptamers, i.e. nucleic acids binding a target molecule specifically and with high affinity without hybridising therewith ; Nucleic acids binding to non-nucleic acids, e.g. aptamers
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    • C07K2317/00Immunoglobulins specific features
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    • C07K2317/41Glycosylation, sialylation, or fucosylation
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    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/10Type of nucleic acid
    • C12N2310/16Aptamers

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Claims (13)

1. Peptid koji se sastoji od slijeda aminokiselina prema SEQ ID br. 42; ili njegova farmaceutski prihvatljiva sol.
2. Peptid prema zahtjevu 1, koji navodi kako peptid uključuje nepeptidne vezove.
3. T-stanični receptor (TCR), po mogućnosti rekombinantni, topljiv ili na membranu vezan T-stanični receptor, koji je reaktivan s HLA ligandom, pri čemu navedeni ligand ima najmanje 88 % identičnosti prema aminokiselinskoj sekvenci u skladu s to SEQ ID br. 42 i po mogućnosti se sastoji od aminokiselinske sekvencije u skladu s SEQ ID br. 42.
4. Antitijelo, posebice topljivo ili na membranu vezano antitijelo, koje posebno prepoznaje peptide prema bilo kojem od zahtjeva 1 ili 2, po mogućnosti peptide prema zahtjevu 1 ili 2 kada se veže za MHC-molekule.
5. Nukleinska kiselina, koja kodira peptid prema bilo kojem od zahtjeva 1 ili 2 za TCR prema zahtjevu 3 ili antitijelo prema zahtjevu 4, opcionalno vezano na heterologni promotorski slijed ili ekspresijski vektor koji eksprimira navedenu nukleinsku kiselinu.
6. Rekombinantna stanica domaćin koja sadrži peptid prema zahtjevu 1 ili 2 ili nukleinsku kiselinu ili ekspresijski vektor prema zahtjevu 5, pri čemu navedena stanica domaćin po mogućnosti predstavlja antigen kao što je dendritička stanica ili gdje je navedena stanica domaćin po mogućnosti T-stanica ili NK stanica.
7. Metoda za proizvodnju peptida prema bilo kojem zahtjevu 1 ili 2 ili za proizvodnju T-staničnih receptora prema zahtjevu 3 ili antitijelo prema zahtjevu 4, metoda koja obuhvaća kultiviranje stanice domaćina prema zahtjevu 6, koja predstavlja peptide prema zahtjevu 1 do 3 ili ekspresivna nukleinska kiselina ili ekspresivni vektor prema zahtjevu 5 i izoliranje peptida ili njegovu varijantu ili TCR ili antitijelo od stanice domaćina ili njezinog medija za kultiviranje.
8. In vitro metoda za proizvodnju aktiviranih T-limfocita, metoda je koja obuhvaća kontaktiranje in vitro T-stanica humanim MHC molekulama klase I s umetnutim antigenima koje se eksprimiraju na površini odgovarajuće stanice koja prezentira antigen ili umjetnom konstrukcijom koja oponaša stanicu koja predstavlja antigen u vremenskom razdoblju dovoljnom da se aktiviraju navedene T-stanice na način svojstven antigenu, pri čemu je navedeni antigen peptid u skladu sa zahtjevom 1 ili 2.
9. Aktivirani T-limfocit, proizveden metodom u skladu s patentnim zahtjevom 8 koji selektivno prepoznaje stanicu koja predstavlja polipeptid koji sadrži sekvenciju aminokiseline sukladno zahtjevu 1 ili 2.
10. Farmaceutski sastav koji sadrži najmanje jedan aktivni sastojak, koji je odabran iz grupe peptida prema bilo kojem od zahtjeva 1 ili 2, nukleinsku kiselinu ili ekspresivni vektor prema zahtjevu 5, stanicu prema zahtjevu 6, aktivirani T-limfocit prema zahtjevu 9 ili antitijelo prema zahtjevu 4 ili T-stanični receptor prema zahtjevu 3 i farmaceutski prihvatljivog nositelja i po potrebi farmaceutski prihvatljivog nositelja i/ili stabilizatora.
11. Peptid prema bilo kojem od zahtjeva 1 ili 2, nukleinska kiselina ili ekspresivni vektor prema zahtjevu 5, stanica prema zahtjevu 6, aktivirani T-limfocit prema zahtjevu 9 ili antitijelo prema zahtjevu 4 ili T-stanični receptor prema zahtjevu 3 za upotrebu u medicini, po mogućnosti za upotrebu u dijagnostici i/ili za liječenje karcinoma ili za upotrebu u proizvodnji lijeka protiv karcinoma.
12. Peptid prema bilo kojem od zahtjeva 1 ili 2, nukleinska kiselina ili ekspresivni vektor prema zahtjevu 5, stanica prema zahtjevu 6, aktivirani T-limfocit prema zahtjevu 9 ili antitijelo prema zahtjevu 4 ili T-stanični receptor prema zahtjevu 3 za uporabu u dijagnostici i/ili za liječenje karcinoma ili za upotrebu u proizvodnji lijeka protiv karcinoma prema zahtjevu 11, pri čemu je karcinom karcinom pluća, karcinoma mozga, karcinom debelog crijeva, želuca, karcinom jetre, karcinom pankreasa, karcinom prostate, leukemija, karcinom dojke, melanoma, karcinom jajnika i karcinom ezofalgusa i drugi karcinom koji pokazuje prekomjernu ekspresiju proteina iz kojeg je izveden peptid prema SEQ ID br. 42.
13. Komplet koji sadrži: a) posudu koja sadrži farmaceutski sastav koji sadrži peptid prema bilo kojem zahtjevu 1 do 2, nukleinsku kiselinu ili ekspresivni vektor prema zahtjevu 5, stanicu prema zahtjevu 6, aktivirani T-limfocit prema zahtjevu 9 ili antitijela prema zahtjevu 4 ili T-stanični receptor prema zahtjevu 3, u otopini ili u liofiliziranom obliku; b) drugu posudu koja sadrži diluens ili otopinu za rekonstituciju za liofiliziranu formulaciju; c) najmanje jedan dodatni peptid iz skupine koja se sastoji od SEQ ID br. 1 do 41 i 43 i d) po potrebi, upute za (i) uporabu otopine ili (ii) rekonstituciju i/ili uporabu liofilizirane formulacije i e) nadalje jedan dodatni (iii) međuspremnik, (iv) diluens, (v) filtar, (vi) igla ili (v) štrcaljka.
HRP20210698TT 2015-12-22 2021-05-05 Peptidi i kombinacija peptida za uporabu u imunoterapiji protiv karcinoma dojke i drugih karcinoma HRP20210698T1 (hr)

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Application Number Priority Date Filing Date Title
US201562270968P 2015-12-22 2015-12-22
GBGB1522667.3A GB201522667D0 (en) 2015-12-22 2015-12-22 Novel peptides and combination of peptides for use in immunotherapy against breast cancer and other cancers
PCT/EP2016/079059 WO2017108345A1 (en) 2015-12-22 2016-11-29 Peptides and combination of peptides for use in immunotherapy against breast cancer and other cancers
EP16802063.4A EP3394084B1 (en) 2015-12-22 2016-11-29 Peptides and combination of peptides for use in immunotherapy against breast cancer and other cancers

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US (11) US10166278B2 (hr)
CL (6) CL2018001531A1 (hr)
CY (1) CY1124224T1 (hr)
HR (1) HRP20210698T1 (hr)
IL (1) IL258599A (hr)
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