Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Nielsen, Lars S., Baer, Alexandra, Müller, Christian, Gregersen, Kristian, Mønster, Nina T., Rasmussen, Søren K., Weilguny, Dietmar, Tolstrup, Anne B.
Formato: Texto
Lenguaje:English
Publicado: Humana Press Inc 2010
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
_version_ 1782182100712030208
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
work_keys_str_mv AT nielsenlarss singlebatchproductionofrecombinanthumanpolyclonalantibodies
AT baeralexandra singlebatchproductionofrecombinanthumanpolyclonalantibodies
AT mullerchristian singlebatchproductionofrecombinanthumanpolyclonalantibodies
AT gregersenkristian singlebatchproductionofrecombinanthumanpolyclonalantibodies
AT mønsterninat singlebatchproductionofrecombinanthumanpolyclonalantibodies
AT rasmussensørenk singlebatchproductionofrecombinanthumanpolyclonalantibodies
AT weilgunydietmar singlebatchproductionofrecombinanthumanpolyclonalantibodies
AT tolstrupanneb singlebatchproductionofrecombinanthumanpolyclonalantibodies