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Exploiting light chains for the scalable generation and platform purification of native human bispecific IgG
Bispecific antibodies enable unique therapeutic approaches but it remains a challenge to produce them at the industrial scale, and the modifications introduced to achieve bispecificity often have an impact on stability and risk of immunogenicity. Here we describe a fully human bispecific IgG devoid...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339886/ https://www.ncbi.nlm.nih.gov/pubmed/25672245 http://dx.doi.org/10.1038/ncomms7113 |
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author | Fischer, Nicolas Elson, Greg Magistrelli, Giovanni Dheilly, Elie Fouque, Nicolas Laurendon, Amélie Gueneau, Franck Ravn, Ulla Depoisier, Jean-François Moine, Valery Raimondi, Sylvain Malinge, Pauline Di Grazia, Laura Rousseau, François Poitevin, Yves Calloud, Sébastien Cayatte, Pierre-Alexis Alcoz, Mathias Pontini, Guillemette Fagète, Séverine Broyer, Lucile Corbier, Marie Schrag, Delphine Didelot, Gérard Bosson, Nicolas Costes, Nessie Cons, Laura Buatois, Vanessa Johnson, Zoe Ferlin, Walter Masternak, Krzysztof Kosco-Vilbois, Marie |
author_facet | Fischer, Nicolas Elson, Greg Magistrelli, Giovanni Dheilly, Elie Fouque, Nicolas Laurendon, Amélie Gueneau, Franck Ravn, Ulla Depoisier, Jean-François Moine, Valery Raimondi, Sylvain Malinge, Pauline Di Grazia, Laura Rousseau, François Poitevin, Yves Calloud, Sébastien Cayatte, Pierre-Alexis Alcoz, Mathias Pontini, Guillemette Fagète, Séverine Broyer, Lucile Corbier, Marie Schrag, Delphine Didelot, Gérard Bosson, Nicolas Costes, Nessie Cons, Laura Buatois, Vanessa Johnson, Zoe Ferlin, Walter Masternak, Krzysztof Kosco-Vilbois, Marie |
author_sort | Fischer, Nicolas |
collection | PubMed |
description | Bispecific antibodies enable unique therapeutic approaches but it remains a challenge to produce them at the industrial scale, and the modifications introduced to achieve bispecificity often have an impact on stability and risk of immunogenicity. Here we describe a fully human bispecific IgG devoid of any modification, which can be produced at the industrial scale, using a platform process. This format, referred to as a κλ-body, is assembled by co-expressing one heavy chain and two different light chains, one κ and one λ. Using ten different targets, we demonstrate that light chains can play a dominant role in mediating specificity and high affinity. The κλ-bodies support multiple modes of action, and their stability and pharmacokinetic properties are indistinguishable from therapeutic antibodies. Thus, the κλ-body represents a unique, fully human format that exploits light-chain variable domains for antigen binding and light-chain constant domains for robust downstream processing, to realize the potential of bispecific antibodies. |
format | Online Article Text |
id | pubmed-4339886 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-43398862015-03-02 Exploiting light chains for the scalable generation and platform purification of native human bispecific IgG Fischer, Nicolas Elson, Greg Magistrelli, Giovanni Dheilly, Elie Fouque, Nicolas Laurendon, Amélie Gueneau, Franck Ravn, Ulla Depoisier, Jean-François Moine, Valery Raimondi, Sylvain Malinge, Pauline Di Grazia, Laura Rousseau, François Poitevin, Yves Calloud, Sébastien Cayatte, Pierre-Alexis Alcoz, Mathias Pontini, Guillemette Fagète, Séverine Broyer, Lucile Corbier, Marie Schrag, Delphine Didelot, Gérard Bosson, Nicolas Costes, Nessie Cons, Laura Buatois, Vanessa Johnson, Zoe Ferlin, Walter Masternak, Krzysztof Kosco-Vilbois, Marie Nat Commun Article Bispecific antibodies enable unique therapeutic approaches but it remains a challenge to produce them at the industrial scale, and the modifications introduced to achieve bispecificity often have an impact on stability and risk of immunogenicity. Here we describe a fully human bispecific IgG devoid of any modification, which can be produced at the industrial scale, using a platform process. This format, referred to as a κλ-body, is assembled by co-expressing one heavy chain and two different light chains, one κ and one λ. Using ten different targets, we demonstrate that light chains can play a dominant role in mediating specificity and high affinity. The κλ-bodies support multiple modes of action, and their stability and pharmacokinetic properties are indistinguishable from therapeutic antibodies. Thus, the κλ-body represents a unique, fully human format that exploits light-chain variable domains for antigen binding and light-chain constant domains for robust downstream processing, to realize the potential of bispecific antibodies. Nature Pub. Group 2015-02-12 /pmc/articles/PMC4339886/ /pubmed/25672245 http://dx.doi.org/10.1038/ncomms7113 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Fischer, Nicolas Elson, Greg Magistrelli, Giovanni Dheilly, Elie Fouque, Nicolas Laurendon, Amélie Gueneau, Franck Ravn, Ulla Depoisier, Jean-François Moine, Valery Raimondi, Sylvain Malinge, Pauline Di Grazia, Laura Rousseau, François Poitevin, Yves Calloud, Sébastien Cayatte, Pierre-Alexis Alcoz, Mathias Pontini, Guillemette Fagète, Séverine Broyer, Lucile Corbier, Marie Schrag, Delphine Didelot, Gérard Bosson, Nicolas Costes, Nessie Cons, Laura Buatois, Vanessa Johnson, Zoe Ferlin, Walter Masternak, Krzysztof Kosco-Vilbois, Marie Exploiting light chains for the scalable generation and platform purification of native human bispecific IgG |
title | Exploiting light chains for the scalable generation and platform purification of native human bispecific IgG |
title_full | Exploiting light chains for the scalable generation and platform purification of native human bispecific IgG |
title_fullStr | Exploiting light chains for the scalable generation and platform purification of native human bispecific IgG |
title_full_unstemmed | Exploiting light chains for the scalable generation and platform purification of native human bispecific IgG |
title_short | Exploiting light chains for the scalable generation and platform purification of native human bispecific IgG |
title_sort | exploiting light chains for the scalable generation and platform purification of native human bispecific igg |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339886/ https://www.ncbi.nlm.nih.gov/pubmed/25672245 http://dx.doi.org/10.1038/ncomms7113 |
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