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Integrated continuous biomanufacturing on pilot scale for acid‐sensitive monoclonal antibodies
In this study, we demonstrated the first, to our knowledge, integrated continuous bioprocess (ICB) designed for the production of acid‐sensitive monoclonal antibodies, prone to aggregate at low pH, on pilot scale. A high cell density perfusion culture, stably maintained at 100 × 10(6) cells/ml, was...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9541590/ https://www.ncbi.nlm.nih.gov/pubmed/35470430 http://dx.doi.org/10.1002/bit.28120 |
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author | Schwarz, Hubert Gomis‐Fons, Joaquín Isaksson, Madelène Scheffel, Julia Andersson, Niklas Andersson, Andreas Castan, Andreas Solbrand, Anita Hober, Sophia Nilsson, Bernt Chotteau, Veronique |
author_facet | Schwarz, Hubert Gomis‐Fons, Joaquín Isaksson, Madelène Scheffel, Julia Andersson, Niklas Andersson, Andreas Castan, Andreas Solbrand, Anita Hober, Sophia Nilsson, Bernt Chotteau, Veronique |
author_sort | Schwarz, Hubert |
collection | PubMed |
description | In this study, we demonstrated the first, to our knowledge, integrated continuous bioprocess (ICB) designed for the production of acid‐sensitive monoclonal antibodies, prone to aggregate at low pH, on pilot scale. A high cell density perfusion culture, stably maintained at 100 × 10(6) cells/ml, was integrated with the downstream process, consisting of a capture step with the recently developed Protein A ligand, Z(Ca); a solvent/detergent‐based virus inactivation; and two ion‐exchange chromatography steps. The use of a mild pH in the downstream process makes this ICB suitable for the purification of acid‐sensitive monoclonal antibodies. Integration and automation of the downstream process were achieved using the Orbit software, and the same equipment and control system were used in initial small‐scale trials and the pilot‐scale downstream process. High recovery yields of around 90% and a productivity close to 1 g purified antibody/L/day were achieved, with a stable glycosylation pattern and efficient removal of impurities, such as host cell proteins and DNA. Finally, negligible levels of antibody aggregates were detected owing to the mild conditions used throughout the process. The present work paves the way for future industrial‐scale integrated continuous biomanufacturing of all types of antibodies, regardless of acid stability. |
format | Online Article Text |
id | pubmed-9541590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95415902022-10-14 Integrated continuous biomanufacturing on pilot scale for acid‐sensitive monoclonal antibodies Schwarz, Hubert Gomis‐Fons, Joaquín Isaksson, Madelène Scheffel, Julia Andersson, Niklas Andersson, Andreas Castan, Andreas Solbrand, Anita Hober, Sophia Nilsson, Bernt Chotteau, Veronique Biotechnol Bioeng ARTICLES In this study, we demonstrated the first, to our knowledge, integrated continuous bioprocess (ICB) designed for the production of acid‐sensitive monoclonal antibodies, prone to aggregate at low pH, on pilot scale. A high cell density perfusion culture, stably maintained at 100 × 10(6) cells/ml, was integrated with the downstream process, consisting of a capture step with the recently developed Protein A ligand, Z(Ca); a solvent/detergent‐based virus inactivation; and two ion‐exchange chromatography steps. The use of a mild pH in the downstream process makes this ICB suitable for the purification of acid‐sensitive monoclonal antibodies. Integration and automation of the downstream process were achieved using the Orbit software, and the same equipment and control system were used in initial small‐scale trials and the pilot‐scale downstream process. High recovery yields of around 90% and a productivity close to 1 g purified antibody/L/day were achieved, with a stable glycosylation pattern and efficient removal of impurities, such as host cell proteins and DNA. Finally, negligible levels of antibody aggregates were detected owing to the mild conditions used throughout the process. The present work paves the way for future industrial‐scale integrated continuous biomanufacturing of all types of antibodies, regardless of acid stability. John Wiley and Sons Inc. 2022-05-07 2022-08 /pmc/articles/PMC9541590/ /pubmed/35470430 http://dx.doi.org/10.1002/bit.28120 Text en © 2022 The Authors. Biotechnology and Bioengineering published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | ARTICLES Schwarz, Hubert Gomis‐Fons, Joaquín Isaksson, Madelène Scheffel, Julia Andersson, Niklas Andersson, Andreas Castan, Andreas Solbrand, Anita Hober, Sophia Nilsson, Bernt Chotteau, Veronique Integrated continuous biomanufacturing on pilot scale for acid‐sensitive monoclonal antibodies |
title | Integrated continuous biomanufacturing on pilot scale for acid‐sensitive monoclonal antibodies |
title_full | Integrated continuous biomanufacturing on pilot scale for acid‐sensitive monoclonal antibodies |
title_fullStr | Integrated continuous biomanufacturing on pilot scale for acid‐sensitive monoclonal antibodies |
title_full_unstemmed | Integrated continuous biomanufacturing on pilot scale for acid‐sensitive monoclonal antibodies |
title_short | Integrated continuous biomanufacturing on pilot scale for acid‐sensitive monoclonal antibodies |
title_sort | integrated continuous biomanufacturing on pilot scale for acid‐sensitive monoclonal antibodies |
topic | ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9541590/ https://www.ncbi.nlm.nih.gov/pubmed/35470430 http://dx.doi.org/10.1002/bit.28120 |
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