HRP20191968T1 - Monoklonska protutijela protiv klaudina-18 za liječenje karcinoma - Google Patents

Monoklonska protutijela protiv klaudina-18 za liječenje karcinoma Download PDF

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Publication number
HRP20191968T1
HRP20191968T1 HRP20191968TT HRP20191968T HRP20191968T1 HR P20191968 T1 HRP20191968 T1 HR P20191968T1 HR P20191968T T HRP20191968T T HR P20191968TT HR P20191968 T HRP20191968 T HR P20191968T HR P20191968 T1 HRP20191968 T1 HR P20191968T1
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Croatia
Prior art keywords
positions
acid sequence
cell
nucleic acid
seq
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HRP20191968TT
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English (en)
Inventor
Ugur Sahin
Özlem TÜRECI
Dirk Usener
Stefan Fritz
Christoph Uherek
Gunda Brandenburg
Harald-Gerhard Geppert
Anja Kristina SCHRÖDER
Philippe Thiel
Original Assignee
Astellas Pharma Inc.
Tron - Translationale Onkologie An Der Universitätsmedizin Der Johannes Gutenberg- Universität Mainz Gemeinnützige Gmbh
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Publication of HRP20191968T1 publication Critical patent/HRP20191968T1/hr

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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
    • C07K16/30Immunoglobulins [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
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Claims (12)

1. In vitro metoda proizvodnje protutijela koja ima sposobnost vezanja za CLD18A2 ali ne za CLD18A1 i po vezanju za CLD18A2 posreduju u uništavanju stanica s T stanicama, pri čemu postupak sadrži korake: (a) promjenu ljudskih stanica domaćina s ekspresijskim vektorom koji eksprimira teški lanac protutijela i ekspresijskim vektorom koji eksprimira laki lanac protutijela ili s ekspresijskim vektorom koji eksprimira oba lanca; i (b) izoliranje i pročišćavanje protutijela koji eksprimira ljudska stanica domaćina; naznačeno time da transformirana ljudska stanica domaćin sadrži: (i) sekvencu nukelinske kiseline koja kodira polipeptid koji sadrži varijabilno područje teškog lanca protutijela (VH) koji sadrži CDR1, CDR2, i CDR3 područja koja sadrže aminokiselinske sekvence položaja 45-52, položaja 70-77, i položaja 116-124 od SEQ ID NO: 117, respektivno; i sekvencu nukleinske kiseline koja kodira polipeptid koji sadrži varijabilni područje lakog lanca protutijela (VL) koji sadrži CDR1, CDR2, i CDR3 područje koje sadrži aminokiselinske sekvence položaja 47-52, položaja 70-72, i položaja 109-117 od SEQ ID NO: 123, respektivno; ili (ii) sekvencu nukleinske kiseline koja kodira polipeptid koji sadrži varijabilno područje teškog lanca protutijela (VH) koji sadrži CDR1, CDR2, i CDR3 područja koja sadrže aminokiselinsku sekvencu položaja 45-52, položaja 70-77, i položaja 116-126 od SEQ ID NO: 116, respektivno; i sekvencu nukleinske kiseline koja kodira polipeptid koji sadrži varijabilni područje lakog lanca protutijela (VL) koje sadrži CDR1, CDR2, i CDR3 područja koja sadrže aminokiselinske sekvence položaja 47-58, položaja 76-78, i položaja 115-123 od SEQ ID NO: 121, respektivno; ili (iii) sekvencu nukleinske kiseline koja kodira polipeptid koji sadrži varijabilno područje teškog lanca protutijela (VH) koji sadrži CDR1, CDR2, i CDR3 područja koja sadrže aminokiselinsku sekvencu položaja 45-52, položaja 70-77, i položaja 116-126 od SEQ ID NO: 118, respektivno; i sekvencu nukleinske kiseline koja kodira polipeptid koji sadrži varijabilno područje lakog lanca protutijela (VL) koji sadrži CDR1, CDR2, i CDR3 područja koji sadrže aminokiselinske sekvence položaja 47-58, položaja 76-78, i položaja 115-123 od SEQ ID NO: 125, respektivno.
2. In vitro metoda sukladno patentnom zahtjevu 1, naznačeno time da je ljudska stanica domaćin HEK293 ćelija, HEK293T stanica, ili limfocitna stanica.
3. In vitro metoda sukladno patentnom zahtjevu 1 ili 2, naznačeno time da ekspresijski vektor sadrži promotor sekvencu, lider sekvencu, sekvencu za inicijaciju translacije, konstantno područje lakog lanca, konstantno područje teškog lanca, 3’ netranslatiranu sekvencu, poliadenilacijsku sekvencu, ili sekvencu za terminiranje transkripcije.
4. In vitro metoda sukladno bilo kojem od patentnih zahtjeva 1 do 3, naznačeno time da su varijabilna područja VH i VL spojeni umjetnim linkerima.
5. In vitro metoda sukladno bilo kojem od patentnih zahtjeva 1 do 4, naznačeno time da su varijabilna područja VH i VL spojeni N- ili C-terminalno s dodatnim proteinskim sekvencama.
6. Rekombinantna nukleinska kiselina operativno poveznaa sa sekvencama za kontrolu ekspresije, pri čemu navedena nukleinska kiselina sadrži sekvencu nukleinske kiseline odabranu iz skupine sastavljene od: (i) sekvence nukleinske kiseline koja kodira polipeptid koji sadrži varijabilno područje teškog lanca koje sadrži aminokiselinsku sekvencu od SEQ ID NO: 134 i varijabilno područje lakog lanca koje sadrži aminokiselinsku sekvencu od SEQ ID NO: 140; (ii) sekvence nukleinske kiseline koja kodira polipeptid koji sadrži varijabilno područje teškog lanca koje sadrži aminokiselinsku sekvencu od SEQ ID NO: 133 i varijabilno područje lakog lanca koje sadrži aminokiselinsku sekvencu od SEQ ID NO: 138; i (iii) sekvence nukleinske kiseline koja kodira polipeptid koji sadrži varijabilno područje teškog lanca koje sadrži aminokiselinsku sekvencu od SEQ ID NO: 135 i varijabilno područje lakog lanca koji ima aminokiselinsku sekvencu od SEQ ID NO: 142 naznačeno time da navedena nukleinska kiselina kodira polipeptid, poželjno protutijelo, koje je sposobno vezivati se za CLD18A2 ali ne za CLD18A1 i nakon vezanja za CLD18A2 posreduje u uništavanju stanica koje eksprimiraju CLD18A2 od strane T stanica.
7. Izolirana ljudska stanica domaćin koja sadrži rekombinantnu nukleinsku kiselinu sukladno patentnom zahtjevu 6.
8. Izolirana ljudska stanica domaćin sukladno patentnom zahtjevu 7, naznačeno time da stanica je HEK293 stanica, HEK293T stanica, ili limfocitna stanica.
9. Protu-CLD18A2 protutijelo eksprimirano od strane izolirane ljudske stanice domaćina sukladno patentnom zahtjevu 7 ili 8, naznačeno time da se protutijelo veže za CLD18A2 ali ne za CLD18A1 i po vezanju za CLD18A2 posreduje u uništavanju stanica koje eksprimiraju CLD18A2 od strane T stanica.
10. In vitro metoda proizvodnje rekombinantne eukariotske stanice domaćina, koji sadrži korake: a. promjene eukariotske stanice s ekspresionim vektorom koji sadrži rekombinantnu nukleinsku kiselinu sukladno patentnom zahtjevu 6; i b. dobivanje promijenjene stanice, naznačeno time da promijenjena stanica sadrži rekombinantnu nukleinsku kiselinu.
11. Metoda sukladno patentnom zahtjevu 10, naznačeno time da rekombinantna stanica domaćin je humana stanica.
12. Metoda sukladno patentnom zahtjevu 10 ili 11, naznačeno time da rekombinantna eukariotska stanica je HEK293 stanica, HEK293T stanica, CHO stanica ili limfocitna stanica.
HRP20191968TT 2005-11-24 2019-10-30 Monoklonska protutijela protiv klaudina-18 za liječenje karcinoma HRP20191968T1 (hr)

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HRP20130451TT HRP20130451T1 (en) 2005-11-24 2013-05-23 Monoclonal antibodies against claudin-18 for treatment of cancer
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HRP20151257TT HRP20151257T1 (hr) 2005-11-24 2015-11-23 Monoklonska protutijela na klaudin-18 za lijeäśenje karcinoma
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