HRP20221383T1 - Kombinacije elemenata ekspresijskog vektora, novi proizvodni postupci dobivanja stanica i njihova uporaba za rekombinantnu proizvodnju polipeptida - Google Patents

Kombinacije elemenata ekspresijskog vektora, novi proizvodni postupci dobivanja stanica i njihova uporaba za rekombinantnu proizvodnju polipeptida Download PDF

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Publication number
HRP20221383T1
HRP20221383T1 HRP20221383TT HRP20221383T HRP20221383T1 HR P20221383 T1 HRP20221383 T1 HR P20221383T1 HR P20221383T T HRP20221383T T HR P20221383TT HR P20221383 T HRP20221383 T HR P20221383T HR P20221383 T1 HRP20221383 T1 HR P20221383T1
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antibody
nucleic acid
acid encoding
expression
cells
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HRP20221383TT
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Peter Michael HUELSMANN
Hendrik Knoetgen
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F. Hoffmann - La Roche Ag
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2851Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the lectin superfamily, e.g. CD23, CD72
    • C07K16/2854Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the lectin superfamily, e.g. CD23, CD72 against selectins, e.g. CD62
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/46Hybrid immunoglobulins
    • C07K16/468Immunoglobulins having two or more different antigen binding sites, e.g. multifunctional antibodies
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • 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
    • C12N15/63Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/85Vectors or expression systems specially adapted for eukaryotic hosts for animal cells
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/10Immunoglobulins specific features characterized by their source of isolation or production
    • C07K2317/14Specific host cells or culture conditions, e.g. components, pH or temperature
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2830/00Vector systems having a special element relevant for transcription
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2830/00Vector systems having a special element relevant for transcription
    • C12N2830/36Vector systems having a special element relevant for transcription being a transcription termination element
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2830/00Vector systems having a special element relevant for transcription
    • C12N2830/42Vector systems having a special element relevant for transcription being an intron or intervening sequence for splicing and/or stability of RNA
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2840/00Vectors comprising a special translation-regulating system
    • C12N2840/20Vectors comprising a special translation-regulating system translation of more than one cistron
    • C12N2840/203Vectors comprising a special translation-regulating system translation of more than one cistron having an IRES

Claims (24)

1. Postupak za odabir rekombinantne stabilne transficirane stanice sisavca naznačen time, da obuhvaća sljedeće korake: a) transficiranje stanice sisavca s ekspresijskim vektorom koji sadrži - prvu ekspresijsku kasetu koja u smjeru od 5' do 3' sadrži promotor hCMV virusa, nukleinsku kiselinu koja kodira laki lanac protutijela, signalni slijed bGH polyA i terminacijski slijed hGT, - drugu ekspresijsku kasetu koja u smjeru od 5' do 3' sadrži promotor hCMV virusa, nukleinsku kiselinu koja kodira teški lanac protutijela, signalni slijed bGH polyA i terminacijski slijed hGT, pri čemu su prva ekspresijska kaseta i druga ekspresijska kaseta raspoređene jednosmjerno, čime se dobiva mnoštvo rekombinantnih stanica sisavca, b) odabiranje iz mnoštva rekombinantnih stanica sisavca (jedne) stabilno transficirane rekombinantne stanice sisavca, pri čemu u staničnim linijama, koje se dobivaju transficiranjem i odabirom stabilnih staničnih klonova, kombinacija signalnog slijeda goveđeg hormona rasta polyA i terminacije humanog gastrina rezultira u poboljšanom prinosu ekspresije protutijela.
2. Postupak prema patentnom zahtjevu 1, naznačen time, da nukleinska kiselina koja kodira laki lanac protutijela i/ili nukleinska kiselina koja kodira teški lanac protutijela sadrži barem jedan intron.
3. Postupak prema bilo kojem od patentnih zahtjeva 1 do 2, naznačen time, da nukleinska kiselina koja kodira laki lanac protutijela i/ili nukleinska kiselina koja kodira teški lanac protutijela jest cDNA.
4. Postupak prema bilo kojem od patentnih zahtjeva 1 do 3, naznačen time, da ekspresijski plazmid nadalje sadrži selekcijski marker.
5. Postupak prema bilo kojem od patentnih zahtjeva 1 do 4, naznačen time, da su ekspresijske kasete i selekcijski marker raspoređeni jednosmjerno.
6. Postupak prema bilo kojem od patentnih zahtjeva 1 do 5, naznačen time, da su ekspresijske kasete raspoređene u nizu LC-HC-SM.
7. Postupak prema bilo kojem od patentnih zahtjeva 1 do 6, naznačen time, da je stanica sisavca odabrana iz CHO stanica, HEK stanica, BHK stanica, NS0 stanica i SP2/0 stanica.
8. Postupak prema bilo kojem od patentnih zahtjeva 1 do 7, naznačen time, da stanica sisavca je CHO stanica za odabir stabilno transficirane stanice.
9. Postupak za proizvodnju protutijela, naznačen time, da obuhvaća sljedeće korake: a) kultivacija stanice sisavca koja sadrži - prvu ekspresijsku kasetu koja u smjeru od 5' do 3' sadrži promotor hCMV virusa, nukleinsku kiselinu koja kodira laki lanac protutijela, signalni slijed bGH polyA i terminacijski slijed hGT, - drugu ekspresijsku kasetu koja u smjeru od 5' do 3' sadrži promotor hCMV virusa, nukleinsku kiselinu koja kodira teški lanac protutijela, signalni slijed bGH polyA i terminacijski slijed hGT, i b) vraćanje protutijela iz stanice ili kultivacijskog medija, pri čemu su prva ekspresijska kaseta i druga ekspresijska kaseta raspoređene jednosmjerno za stabilnu proizvodnju protutijela.
10. Postupak prema patentnom zahtjevu 9, naznačen time, da nukleinska kiselina koja kodira laki lanac protutijela i/ili nukleinska kiselina koja kodira teški lanac protutijela sadrži barem jedan intron.
11. Postupak prema bilo kojem od patentnih zahtjeva 9 do 10, naznačen time, da nukleinska kiselina koja kodira laki lanac protutijela i/ili nukleinska kiselina koja kodira teški lanac protutijela jest cDNA.
12. Postupak prema bilo kojem od patentnih zahtjeva 9 do 11, naznačen time, da ekspresijski plazmid nadalje sadrži selekcijski marker.
13. Postupak prema bilo kojem od patentnih zahtjeva 9 do 12, naznačen time, da su ekspresijske kasete i selekcijski marker raspoređeni jednosmjerno.
14. Postupak prema bilo kojem od patentnih zahtjeva 9 do 13, naznačen time, da su ekspresijske kasete raspoređene u nizu LC-HC-SM.
15. Postupak prema bilo kojem od patentnih zahtjeva 9 do 14, naznačen time, da je stanica sisavca odabrana iz CHO stanica, HEK stanica, BHK stanica, NS0 stanica i SP2/0 stanica.
16. Postupak prema bilo kojem od patentnih zahtjeva 9 do 15, naznačen time, da stanica sisavca je CHO stanica za stabilnu proizvodnju protutijela.
17. Ekspresijski vektor, naznačen time, da sadrži - prvu ekspresijsku kasetu koja u smjeru od 5' do 3' sadrži promotor hCMV virusa, nukleinsku kiselinu koja kodira laki lanac protutijela, signalni slijed bGH polyA i terminacijski slijed hGT, - drugu ekspresijsku kasetu koja u smjeru od 5' do 3' sadrži promotor hCMV virusa, nukleinsku kiselinu koja kodira teški lanac protutijela, signalni slijed bGH polyA i terminacijski slijed hGT.
18. Ekspresijski vektor prema patentnom zahtjevu 17, naznačen time, da nukleinska kiselina koja kodira laki lanac protutijela i/ili nukleinska kiselina koja kodira teški lanac protutijela sadrži barem jedan intron.
19. Ekspresijski vektor prema bilo kojem od patentnih zahtjeva 17 do 18, naznačen time, da nukleinska kiselina koja kodira laki lanac protutijela i/ili nukleinska kiselina koja kodira teški lanac protutijela jest cDNA.
20. Ekspresijski vektor prema bilo kojem od patentnih zahtjeva 17 do 19, naznačen time, da su prva ekspresijska kaseta i druga ekspresijska kaseta raspoređene jednosmjerno za odabir stabilno transficirane stanice.
21. Ekspresijski vektor prema bilo kojem od patentnih zahtjeva 17 do 20, naznačen time, da ekspresijski plazmid nadalje sadrži selekcijski marker.
22. Ekspresijski vektor prema bilo kojem od patentnih zahtjeva 17 do 21, naznačen time, da su ekspresijske kasete i selekcijski marker raspoređeni jednosmjerno.
23. Ekspresijski vektor prema bilo kojem od patentnih zahtjeva 17 do 22, naznačen time, da su ekspresijske kasete raspoređene u nizu LC-HC-SM.
24. Eukariotska stanica, naznačena time, da sadrži ekspresijski vektor prema bilo kojem od patentnih zahtjeva 17 do 22.
HRP20221383TT 2011-12-22 2012-12-19 Kombinacije elemenata ekspresijskog vektora, novi proizvodni postupci dobivanja stanica i njihova uporaba za rekombinantnu proizvodnju polipeptida HRP20221383T1 (hr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP11195361 2011-12-22
PCT/EP2012/076203 WO2013092743A2 (en) 2011-12-22 2012-12-19 Expression vector element combinations, novel production cell generation methods and their use for the recombinant production of polypeptides
EP12810245.6A EP2794651B1 (en) 2011-12-22 2012-12-19 Expression vector element combinations, novel production cell generation methods and their use for the recombinant production of polypeptides

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HRP20221383T1 true HRP20221383T1 (hr) 2023-01-06

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US (2) US20160208284A1 (hr)
EP (2) EP2794651B1 (hr)
JP (4) JP6096802B2 (hr)
KR (4) KR102048556B1 (hr)
CN (4) CN113881702A (hr)
CA (2) CA2854249C (hr)
ES (1) ES2930215T3 (hr)
HK (1) HK1200848A1 (hr)
HR (1) HRP20221383T1 (hr)
MX (2) MX355624B (hr)
PL (1) PL2794651T3 (hr)
RU (2) RU2639519C2 (hr)
SG (3) SG11201403443WA (hr)
WO (1) WO2013092743A2 (hr)

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