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.Info
- 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
- Authority
- MX
- Mexico
- Prior art keywords
- domain
- light chain
- heavy chain
- chain variable
- variable domain
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2803—Immunoglobulins [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
- C07K16/2809—Immunoglobulins [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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/46—Hybrid immunoglobulins
- C07K16/468—Immunoglobulins having two or more different antigen binding sites, e.g. multifunctional antibodies
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
- C12N15/85—Vectors or expression systems specially adapted for eukaryotic hosts for animal cells
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/87—Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation
- C12N15/90—Stable introduction of foreign DNA into chromosome
- C12N15/902—Stable introduction of foreign DNA into chromosome using homologous recombination
- C12N15/907—Stable introduction of foreign DNA into chromosome using homologous recombination in mammalian cells
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/10—Immunoglobulins specific features characterized by their source of isolation or production
- C07K2317/14—Specific host cells or culture conditions, e.g. components, pH or temperature
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
- C07K2317/31—Immunoglobulins specific features characterized by aspects of specificity or valency multispecific
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
- C07K2317/35—Valency
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/52—Constant or Fc region; Isotype
- C07K2317/526—CH3 domain
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/55—Fab or Fab'
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/60—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
- C07K2317/64—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments comprising a combination of variable region and constant region components
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2800/00—Nucleic acids vectors
- C12N2800/30—Vector 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.
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) |
Family Cites Families (36)
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US4676980A (en) | 1985-09-23 | 1987-06-30 | The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services | Target specific cross-linked heteroantibodies |
AU600575B2 (en) | 1987-03-18 | 1990-08-16 | Sb2, Inc. | Altered antibodies |
WO1992008796A1 (en) | 1990-11-13 | 1992-05-29 | Immunex Corporation | Bifunctional selectable fusion genes |
WO1993008829A1 (en) | 1991-11-04 | 1993-05-13 | The Regents Of The University Of California | Compositions that mediate killing of hiv-infected cells |
CA2163427A1 (en) | 1993-05-21 | 1994-12-08 | Stephen D. Lupton | Bifunctional selectable fusion genes based on the cytosine deaminase (cd) gene |
US5731168A (en) | 1995-03-01 | 1998-03-24 | Genentech, Inc. | Method for making heteromultimeric polypeptides |
LT2857516T (lt) | 2000-04-11 | 2017-09-11 | Genentech, Inc. | Multivalentiniai antikūnai ir jų panaudojimas |
MX2007000644A (es) | 2004-07-20 | 2007-03-28 | Symphogen As | Anticuerpo policlonal recombinante anti-rhesus d y metodos de fabricacion. |
BRPI0615397B1 (pt) * | 2005-08-26 | 2023-10-03 | Roche Glycart Ag | Anticorpo anti-cd20, composição farmacêutica que o contém e uso do mesmo |
US9266967B2 (en) | 2007-12-21 | 2016-02-23 | Hoffmann-La Roche, Inc. | Bivalent, bispecific antibodies |
US8242247B2 (en) | 2007-12-21 | 2012-08-14 | Hoffmann-La Roche Inc. | Bivalent, bispecific antibodies |
US8227577B2 (en) | 2007-12-21 | 2012-07-24 | Hoffman-La Roche Inc. | Bivalent, bispecific antibodies |
US20090162359A1 (en) | 2007-12-21 | 2009-06-25 | Christian Klein | Bivalent, bispecific antibodies |
ES2774337T3 (es) | 2008-01-07 | 2020-07-20 | Amgen Inc | Método para fabricación de moléculas heterodímeras Fc de anticuerpos utilizando efectos de conducción electrostática |
AU2010230563A1 (en) | 2009-04-02 | 2011-09-22 | Roche Glycart Ag | Multispecific antibodies comprising full length antibodies and single chain Fab fragments |
US20100256340A1 (en) | 2009-04-07 | 2010-10-07 | Ulrich Brinkmann | Trivalent, bispecific antibodies |
MX2011011925A (es) | 2009-05-27 | 2011-12-06 | Hoffmann La Roche | Anticuerpos triespecificos o tetraespecificos. |
US9676845B2 (en) | 2009-06-16 | 2017-06-13 | Hoffmann-La Roche, Inc. | Bispecific antigen binding proteins |
US8703132B2 (en) | 2009-06-18 | 2014-04-22 | Hoffmann-La Roche, Inc. | Bispecific, tetravalent antigen binding proteins |
RS64179B1 (sr) | 2011-05-27 | 2023-05-31 | Hoffmann La Roche | Dvostruko ciljanje |
WO2013006142A1 (en) | 2011-07-05 | 2013-01-10 | Nanyang Technological University | A novel process and reagent for rapid genetic alterations in eukaryotic cells |
LT2748202T (lt) | 2011-08-23 | 2018-09-25 | Roche Glycart Ag | Bispecifinės antigeną surišančios molekulės |
EP3315514A1 (en) | 2012-08-29 | 2018-05-02 | F. Hoffmann-La Roche AG | Blood brain barrier shuttle |
EP2961771B1 (en) * | 2013-02-26 | 2020-01-01 | Roche Glycart AG | Bispecific t cell activating antigen binding molecules specific to cd3 and cea |
CN104342453A (zh) | 2013-08-06 | 2015-02-11 | 深圳先进技术研究院 | 含基因工程抗体基因表达盒的微环dna重组母质粒、含该表达盒的微环dna及应用 |
EP2982692A1 (en) | 2014-08-04 | 2016-02-10 | EngMab AG | Bispecific antibodies against CD3epsilon and BCMA |
NZ766556A (en) * | 2014-08-04 | 2024-02-23 | Hoffmann La Roche | Bispecific t cell activating antigen binding molecules |
CA2963696A1 (en) | 2014-10-09 | 2016-04-14 | Engmab Ag | Bispecific antibodies against cd3epsilon and ror1 for use in the treatment of ovarian cancer |
CN107074955B (zh) | 2014-11-20 | 2021-06-22 | 豪夫迈·罗氏有限公司 | 针对FolR1和CD3的T细胞活化性双特异性抗原结合分子 |
JP6930929B2 (ja) | 2015-07-03 | 2021-09-01 | エシロール アンテルナショナルEssilor International | 拡張現実のための方法とシステム |
CR20180162A (es) * | 2015-10-02 | 2018-05-25 | Hoffmann La Roche | Moléculas biespecíficas de unión a antígeno activadoras de células t |
CN110572195B (zh) | 2016-03-25 | 2020-11-24 | 华为技术有限公司 | 一种天线端口的指示方法和装置 |
BR112018071285A2 (pt) | 2016-04-20 | 2019-02-12 | Regeneron Pharma | célula, conjunto de vetores, vetor, sistema, e, método |
KR102630357B1 (ko) | 2017-02-17 | 2024-01-30 | 론자 리미티드 | 단백질 발현이 어려운 다중-부위 ssi 세포 |
PE20191360A1 (es) | 2017-03-10 | 2019-10-01 | Hoffmann La Roche | Metodo para producir anticuerpos multiespecificos |
JP7208380B2 (ja) | 2018-10-26 | 2023-01-18 | エフ.ホフマン-ラ ロシュ アーゲー | リコンビナーゼ媒介性カセット交換を使用した多重特異性抗体スクリーニング法 |
-
2020
- 2020-06-17 KR KR1020227001603A patent/KR20220024637A/ko not_active Application Discontinuation
- 2020-06-17 WO PCT/EP2020/066678 patent/WO2020254352A1/en unknown
- 2020-06-17 CA CA3140287A patent/CA3140287A1/en active Pending
- 2020-06-17 EP EP20734131.4A patent/EP3986925A1/en active Pending
- 2020-06-17 BR BR112021025401A patent/BR112021025401A2/pt unknown
- 2020-06-17 AU AU2020296247A patent/AU2020296247A1/en active Pending
- 2020-06-17 JP JP2021575263A patent/JP7446342B2/ja active Active
- 2020-06-17 CN CN202080044538.6A patent/CN114008212A/zh active Pending
- 2020-06-17 MX MX2021015540A patent/MX2021015540A/es unknown
-
2021
- 2021-12-13 IL IL288968A patent/IL288968A/en unknown
- 2021-12-16 US US17/553,516 patent/US20220169729A1/en active Pending
-
2023
- 2023-11-29 JP JP2023201315A patent/JP2024026208A/ja active Pending
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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