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Development of an automated manufacturing process for large-scale production of autologous T cell therapies
Engineered T cell therapies have shown significant clinical success. However, current manufacturing capabilities present a challenge in bringing these therapies to patients. Furthermore, the cost of development and manufacturing is still extremely high due to complexity of the manufacturing process....
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10544074/ https://www.ncbi.nlm.nih.gov/pubmed/37790245 http://dx.doi.org/10.1016/j.omtm.2023.101114 |
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author | Francis, Natalie Braun, Marion Neagle, Sarah Peiffer, Sabine Bohn, Alexander Rosenthal, Alexander Olbrich, Tanita Lollies, Sophia Ilsmann, Keijo Hauck, Carola Gerstmayer, Bernhard Weber, Silvio Kirkpatrick, Aileen |
author_facet | Francis, Natalie Braun, Marion Neagle, Sarah Peiffer, Sabine Bohn, Alexander Rosenthal, Alexander Olbrich, Tanita Lollies, Sophia Ilsmann, Keijo Hauck, Carola Gerstmayer, Bernhard Weber, Silvio Kirkpatrick, Aileen |
author_sort | Francis, Natalie |
collection | PubMed |
description | Engineered T cell therapies have shown significant clinical success. However, current manufacturing capabilities present a challenge in bringing these therapies to patients. Furthermore, the cost of development and manufacturing is still extremely high due to complexity of the manufacturing process. Increased automation can improve quality and reproducibility while reducing costs through minimizing hands-on operator time, allowing parallel manufacture of multiple products, and reducing the complexity of technology transfer. In this article, we describe the results of a strategic alliance between GSK and Miltenyi Biotec to develop a closed, automated manufacturing process using the CliniMACS Prodigy for autologous T cell therapy products that can deliver a high number of cells suitable for treating solid tumor indications and compatible with cryopreserved apheresis and drug product. We demonstrate the ability of the T cell Transduction – Large Scale process to deliver a significantly higher cell number than the existing process, achieving 1.5 × 10(10) cells after 12 days of expansion, without affecting other product attributes. We demonstrate successful technology transfer of this robust process into three manufacturing facilities. |
format | Online Article Text |
id | pubmed-10544074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-105440742023-10-03 Development of an automated manufacturing process for large-scale production of autologous T cell therapies Francis, Natalie Braun, Marion Neagle, Sarah Peiffer, Sabine Bohn, Alexander Rosenthal, Alexander Olbrich, Tanita Lollies, Sophia Ilsmann, Keijo Hauck, Carola Gerstmayer, Bernhard Weber, Silvio Kirkpatrick, Aileen Mol Ther Methods Clin Dev Original Article Engineered T cell therapies have shown significant clinical success. However, current manufacturing capabilities present a challenge in bringing these therapies to patients. Furthermore, the cost of development and manufacturing is still extremely high due to complexity of the manufacturing process. Increased automation can improve quality and reproducibility while reducing costs through minimizing hands-on operator time, allowing parallel manufacture of multiple products, and reducing the complexity of technology transfer. In this article, we describe the results of a strategic alliance between GSK and Miltenyi Biotec to develop a closed, automated manufacturing process using the CliniMACS Prodigy for autologous T cell therapy products that can deliver a high number of cells suitable for treating solid tumor indications and compatible with cryopreserved apheresis and drug product. We demonstrate the ability of the T cell Transduction – Large Scale process to deliver a significantly higher cell number than the existing process, achieving 1.5 × 10(10) cells after 12 days of expansion, without affecting other product attributes. We demonstrate successful technology transfer of this robust process into three manufacturing facilities. American Society of Gene & Cell Therapy 2023-09-16 /pmc/articles/PMC10544074/ /pubmed/37790245 http://dx.doi.org/10.1016/j.omtm.2023.101114 Text en © 2023 GlaxoSmithKline plc https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Francis, Natalie Braun, Marion Neagle, Sarah Peiffer, Sabine Bohn, Alexander Rosenthal, Alexander Olbrich, Tanita Lollies, Sophia Ilsmann, Keijo Hauck, Carola Gerstmayer, Bernhard Weber, Silvio Kirkpatrick, Aileen Development of an automated manufacturing process for large-scale production of autologous T cell therapies |
title | Development of an automated manufacturing process for large-scale production of autologous T cell therapies |
title_full | Development of an automated manufacturing process for large-scale production of autologous T cell therapies |
title_fullStr | Development of an automated manufacturing process for large-scale production of autologous T cell therapies |
title_full_unstemmed | Development of an automated manufacturing process for large-scale production of autologous T cell therapies |
title_short | Development of an automated manufacturing process for large-scale production of autologous T cell therapies |
title_sort | development of an automated manufacturing process for large-scale production of autologous t cell therapies |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10544074/ https://www.ncbi.nlm.nih.gov/pubmed/37790245 http://dx.doi.org/10.1016/j.omtm.2023.101114 |
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