MX2021015540A - Metodo para la generacion de una celula que expresa un anticuerpo trivalente mediante la integracion dirigida de multiples casetes de expresion en una organizacion definida. - Google Patents

Metodo para la generacion de una celula que expresa un anticuerpo trivalente mediante la integracion dirigida de multiples casetes de expresion en una organizacion definida.

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Publication number
MX2021015540A
MX2021015540A MX2021015540A MX2021015540A MX2021015540A MX 2021015540 A MX2021015540 A MX 2021015540A MX 2021015540 A MX2021015540 A MX 2021015540A MX 2021015540 A MX2021015540 A MX 2021015540A MX 2021015540 A MX2021015540 A MX 2021015540A
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MX
Mexico
Prior art keywords
domain
light chain
heavy chain
chain variable
variable domain
Prior art date
Application number
MX2021015540A
Other languages
English (en)
Inventor
Ulrich Goepfert
Johannes Auer
Monika Popp
Christina-Lisa Hoeck
Original Assignee
Hoffmann La Roche
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Publication date
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of MX2021015540A publication Critical patent/MX2021015540A/es

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    • 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
    • C07K16/2803Immunoglobulins [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
    • C07K16/2809Immunoglobulins [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 the T-cell receptor (TcR)-CD3 complex
    • 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
    • C07K16/46Hybrid 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
    • 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
    • C12N15/87Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation
    • C12N15/90Stable introduction of foreign DNA into chromosome
    • C12N15/902Stable introduction of foreign DNA into chromosome using homologous recombination
    • C12N15/907Stable introduction of foreign DNA into chromosome using homologous recombination in mammalian 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
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/30Immunoglobulins specific features characterized by aspects of specificity or valency
    • C07K2317/31Immunoglobulins specific features characterized by aspects of specificity or valency multispecific
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/30Immunoglobulins specific features characterized by aspects of specificity or valency
    • C07K2317/35Valency
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/50Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/52Constant or Fc region; Isotype
    • C07K2317/526CH3 domain
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/50Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/55Fab or Fab'
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/60Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
    • C07K2317/64Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments comprising a combination of variable region and constant region components
    • 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
    • C12N2800/00Nucleic acids vectors
    • C12N2800/30Vector systems comprising sequences for excision in presence of a recombinase, e.g. loxP or FRT

Abstract

La presente invención se refiere a un método para producir un anticuerpo trivalente que comprende las etapas de cultivar una célula de mamífero que comprende un ácido desoxirribonucleico que codifica el anticuerpo trivalente, y recuperar el anticuerpo trivalente de la célula o del medio de cultivo, en donde el ácido desoxirribonucleico que codifica el anticuerpo trivalente está integrado de forma estable en el genoma de la célula de mamífero y comprende en dirección 5' a 3' un primer casete de expresión que codifica la primera cadena pesada, un segundo casete de expresión que codifica la primera cadena ligera, un tercer casete de expresión que codifica la primera cadena ligera, un cuarto casete de expresión que codifica la segunda cadena pesada, un quinto casete de expresión que codifica la segunda cadena ligera, y un sexto casete de expresión que codifica la segunda cadena ligera, en donde la primera cadena pesada comprende desde el extremo N hasta el C un primer dominio variable de la cadena pesada, un dominio CH1, un primer dominio variable de la cadena ligera, un dominio CH1, una región bisagra, un dominio CH2 y un dominio CH3, la segunda cadena pesada comprende desde el extremo N hasta el C el primer dominio variable de la cadena pesada, un dominio CH1, una región bisagra, un dominio CH2 y un dominio CH3, la primera cadena ligera comprende desde el extremo N hasta el C un segundo dominio variable de la cadena pesada y un dominio CL, y la segunda cadena ligera comprende desde el extremo N hasta el C un segundo dominio variable de la cadena ligera y un dominio CL, en donde el primer dominio variable de la cadena pesada y el segundo dominio variable de la cadena ligera forman un primer sitio de unión y el segundo dominio variable de la cadena pesada y el primer dominio variable de la cadena ligera forman un segundo sitio de unión.
MX2021015540A 2019-06-19 2020-06-17 Metodo para la generacion de una celula que expresa un anticuerpo trivalente mediante la integracion dirigida de multiples casetes de expresion en una organizacion definida. MX2021015540A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP19181095 2019-06-19
PCT/EP2020/066678 WO2020254352A1 (en) 2019-06-19 2020-06-17 Method for the generation of a trivalent antibody expressing cell by targeted integration of multiple expression cassettes in a defined organization

Publications (1)

Publication Number Publication Date
MX2021015540A true MX2021015540A (es) 2022-02-10

Family

ID=67060256

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2021015540A MX2021015540A (es) 2019-06-19 2020-06-17 Metodo para la generacion de una celula que expresa un anticuerpo trivalente mediante la integracion dirigida de multiples casetes de expresion en una organizacion definida.

Country Status (11)

Country Link
US (1) US20220169729A1 (es)
EP (1) EP3986925A1 (es)
JP (2) JP7446342B2 (es)
KR (1) KR20220024637A (es)
CN (1) CN114008212A (es)
AU (1) AU2020296247A1 (es)
BR (1) BR112021025401A2 (es)
CA (1) CA3140287A1 (es)
IL (1) IL288968A (es)
MX (1) MX2021015540A (es)
WO (1) WO2020254352A1 (es)

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Also Published As

Publication number Publication date
BR112021025401A2 (pt) 2022-02-01
JP2022537334A (ja) 2022-08-25
US20220169729A1 (en) 2022-06-02
JP7446342B2 (ja) 2024-03-08
WO2020254352A1 (en) 2020-12-24
EP3986925A1 (en) 2022-04-27
IL288968A (en) 2022-02-01
CA3140287A1 (en) 2020-12-24
KR20220024637A (ko) 2022-03-03
CN114008212A (zh) 2022-02-01
JP2024026208A (ja) 2024-02-28
AU2020296247A1 (en) 2021-12-23

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