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Single-Batch Production of Recombinant Human Polyclonal Antibodies
We have previously described the development and implementation of a strategy for production of recombinant polyclonal antibodies (rpAb) in single batches employing CHO cells generated by site-specific integration, the Sympress(TM) I technology. The Sympress(TM) I technology is implemented at indust...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Humana Press Inc
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2881207/ https://www.ncbi.nlm.nih.gov/pubmed/20306237 http://dx.doi.org/10.1007/s12033-010-9270-9 |
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author | Nielsen, Lars S. Baer, Alexandra Müller, Christian Gregersen, Kristian Mønster, Nina T. Rasmussen, Søren K. Weilguny, Dietmar Tolstrup, Anne B. |
author_facet | Nielsen, Lars S. Baer, Alexandra Müller, Christian Gregersen, Kristian Mønster, Nina T. Rasmussen, Søren K. Weilguny, Dietmar Tolstrup, Anne B. |
author_sort | Nielsen, Lars S. |
collection | PubMed |
description | We have previously described the development and implementation of a strategy for production of recombinant polyclonal antibodies (rpAb) in single batches employing CHO cells generated by site-specific integration, the Sympress(TM) I technology. The Sympress(TM) I technology is implemented at industrial scale, supporting a phase II clinical development program. Production of recombinant proteins by site-specific integration, which is based on incorporation of a single copy of the gene of interest, makes the Sympress(TM) I technology best suited to support niche indications. To improve titers while maintaining a cost-efficient, highly reproducible single-batch manufacturing mode, we have evaluated a number of different approaches. The most successful results were obtained using random integration in a new producer cell termed ECHO, a CHO DG44 cell derivative engineered for improved productivity at Symphogen. This new expression process is termed the Sympress(TM) II technology. Here we describe proof-of-principle data demonstrating the feasibility of the Sympress(TM) II technology for single-batch rpAb manufacturing using two model systems each composed of six target-specific antibodies. The compositional stability and the batch-to-batch reproducibility of rpAb produced by the ECHO cells were at least as good as observed previously using site-specific integration technology. Furthermore, the new process had a significant titer increase. |
format | Text |
id | pubmed-2881207 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Humana Press Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-28812072010-06-10 Single-Batch Production of Recombinant Human Polyclonal Antibodies Nielsen, Lars S. Baer, Alexandra Müller, Christian Gregersen, Kristian Mønster, Nina T. Rasmussen, Søren K. Weilguny, Dietmar Tolstrup, Anne B. Mol Biotechnol Research We have previously described the development and implementation of a strategy for production of recombinant polyclonal antibodies (rpAb) in single batches employing CHO cells generated by site-specific integration, the Sympress(TM) I technology. The Sympress(TM) I technology is implemented at industrial scale, supporting a phase II clinical development program. Production of recombinant proteins by site-specific integration, which is based on incorporation of a single copy of the gene of interest, makes the Sympress(TM) I technology best suited to support niche indications. To improve titers while maintaining a cost-efficient, highly reproducible single-batch manufacturing mode, we have evaluated a number of different approaches. The most successful results were obtained using random integration in a new producer cell termed ECHO, a CHO DG44 cell derivative engineered for improved productivity at Symphogen. This new expression process is termed the Sympress(TM) II technology. Here we describe proof-of-principle data demonstrating the feasibility of the Sympress(TM) II technology for single-batch rpAb manufacturing using two model systems each composed of six target-specific antibodies. The compositional stability and the batch-to-batch reproducibility of rpAb produced by the ECHO cells were at least as good as observed previously using site-specific integration technology. Furthermore, the new process had a significant titer increase. Humana Press Inc 2010-03-20 2010 /pmc/articles/PMC2881207/ /pubmed/20306237 http://dx.doi.org/10.1007/s12033-010-9270-9 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Research Nielsen, Lars S. Baer, Alexandra Müller, Christian Gregersen, Kristian Mønster, Nina T. Rasmussen, Søren K. Weilguny, Dietmar Tolstrup, Anne B. Single-Batch Production of Recombinant Human Polyclonal Antibodies |
title | Single-Batch Production of Recombinant Human Polyclonal Antibodies |
title_full | Single-Batch Production of Recombinant Human Polyclonal Antibodies |
title_fullStr | Single-Batch Production of Recombinant Human Polyclonal Antibodies |
title_full_unstemmed | Single-Batch Production of Recombinant Human Polyclonal Antibodies |
title_short | Single-Batch Production of Recombinant Human Polyclonal Antibodies |
title_sort | single-batch production of recombinant human polyclonal antibodies |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2881207/ https://www.ncbi.nlm.nih.gov/pubmed/20306237 http://dx.doi.org/10.1007/s12033-010-9270-9 |
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