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Transgenic goats producing an improved version of cetuximab in milk
Therapeutic monoclonal antibodies (mAbs) represent one of the most important classes of pharmaceutical proteins to treat human diseases. Most are produced in cultured mammalian cells which is expensive, limiting their availability. Goats, striking a good balance between a relatively short generation...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7655094/ https://www.ncbi.nlm.nih.gov/pubmed/33205005 http://dx.doi.org/10.1096/fba.2020-00059 |
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author | Laible, Götz Cole, Sally Brophy, Brigid Maclean, Paul How Chen, Li Pollock, Dan P. Cavacini, Lisa Fournier, Nathalie De Romeuf, Christophe Masiello, Nicholas C. Gavin, William G. Wells, David N. Meade, Harry M. |
author_facet | Laible, Götz Cole, Sally Brophy, Brigid Maclean, Paul How Chen, Li Pollock, Dan P. Cavacini, Lisa Fournier, Nathalie De Romeuf, Christophe Masiello, Nicholas C. Gavin, William G. Wells, David N. Meade, Harry M. |
author_sort | Laible, Götz |
collection | PubMed |
description | Therapeutic monoclonal antibodies (mAbs) represent one of the most important classes of pharmaceutical proteins to treat human diseases. Most are produced in cultured mammalian cells which is expensive, limiting their availability. Goats, striking a good balance between a relatively short generation time and copious milk yield, present an alternative platform for the cost‐effective, flexible, large‐scale production of therapeutic mAbs. Here, we focused on cetuximab, a mAb against epidermal growth factor receptor, that is commercially produced under the brand name Erbitux and approved for anti‐cancer treatments. We generated several transgenic goat lines that produce cetuximab in their milk. Two lines were selected for detailed characterization. Both showed stable genotypes and cetuximab production levels of up to 10 g/L. The mAb could be readily purified and showed improved characteristics compared to Erbitux. The goat‐produced cetuximab (gCetuximab) lacked a highly immunogenic epitope that is part of Erbitux. Moreover, it showed enhanced binding to CD16 and increased antibody‐dependent cell‐dependent cytotoxicity compared to Erbitux. This indicates that these goats produce an improved cetuximab version with the potential for enhanced effectiveness and better safety profile compared to treatments with Erbitux. In addition, our study validates transgenic goats as an excellent platform for large‐scale production of therapeutic mAbs. |
format | Online Article Text |
id | pubmed-7655094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76550942020-11-16 Transgenic goats producing an improved version of cetuximab in milk Laible, Götz Cole, Sally Brophy, Brigid Maclean, Paul How Chen, Li Pollock, Dan P. Cavacini, Lisa Fournier, Nathalie De Romeuf, Christophe Masiello, Nicholas C. Gavin, William G. Wells, David N. Meade, Harry M. FASEB Bioadv Research Articles Therapeutic monoclonal antibodies (mAbs) represent one of the most important classes of pharmaceutical proteins to treat human diseases. Most are produced in cultured mammalian cells which is expensive, limiting their availability. Goats, striking a good balance between a relatively short generation time and copious milk yield, present an alternative platform for the cost‐effective, flexible, large‐scale production of therapeutic mAbs. Here, we focused on cetuximab, a mAb against epidermal growth factor receptor, that is commercially produced under the brand name Erbitux and approved for anti‐cancer treatments. We generated several transgenic goat lines that produce cetuximab in their milk. Two lines were selected for detailed characterization. Both showed stable genotypes and cetuximab production levels of up to 10 g/L. The mAb could be readily purified and showed improved characteristics compared to Erbitux. The goat‐produced cetuximab (gCetuximab) lacked a highly immunogenic epitope that is part of Erbitux. Moreover, it showed enhanced binding to CD16 and increased antibody‐dependent cell‐dependent cytotoxicity compared to Erbitux. This indicates that these goats produce an improved cetuximab version with the potential for enhanced effectiveness and better safety profile compared to treatments with Erbitux. In addition, our study validates transgenic goats as an excellent platform for large‐scale production of therapeutic mAbs. John Wiley and Sons Inc. 2020-08-30 /pmc/articles/PMC7655094/ /pubmed/33205005 http://dx.doi.org/10.1096/fba.2020-00059 Text en © 2020 The Authors. FASEB BioAdvances published by the Federation of American Societies for Experimental Biology This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles Laible, Götz Cole, Sally Brophy, Brigid Maclean, Paul How Chen, Li Pollock, Dan P. Cavacini, Lisa Fournier, Nathalie De Romeuf, Christophe Masiello, Nicholas C. Gavin, William G. Wells, David N. Meade, Harry M. Transgenic goats producing an improved version of cetuximab in milk |
title | Transgenic goats producing an improved version of cetuximab in milk |
title_full | Transgenic goats producing an improved version of cetuximab in milk |
title_fullStr | Transgenic goats producing an improved version of cetuximab in milk |
title_full_unstemmed | Transgenic goats producing an improved version of cetuximab in milk |
title_short | Transgenic goats producing an improved version of cetuximab in milk |
title_sort | transgenic goats producing an improved version of cetuximab in milk |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7655094/ https://www.ncbi.nlm.nih.gov/pubmed/33205005 http://dx.doi.org/10.1096/fba.2020-00059 |
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