Cargando…

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....

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2023
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
_version_ 1785114424452841472
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
work_keys_str_mv AT francisnatalie developmentofanautomatedmanufacturingprocessforlargescaleproductionofautologoustcelltherapies
AT braunmarion developmentofanautomatedmanufacturingprocessforlargescaleproductionofautologoustcelltherapies
AT neaglesarah developmentofanautomatedmanufacturingprocessforlargescaleproductionofautologoustcelltherapies
AT peiffersabine developmentofanautomatedmanufacturingprocessforlargescaleproductionofautologoustcelltherapies
AT bohnalexander developmentofanautomatedmanufacturingprocessforlargescaleproductionofautologoustcelltherapies
AT rosenthalalexander developmentofanautomatedmanufacturingprocessforlargescaleproductionofautologoustcelltherapies
AT olbrichtanita developmentofanautomatedmanufacturingprocessforlargescaleproductionofautologoustcelltherapies
AT lolliessophia developmentofanautomatedmanufacturingprocessforlargescaleproductionofautologoustcelltherapies
AT ilsmannkeijo developmentofanautomatedmanufacturingprocessforlargescaleproductionofautologoustcelltherapies
AT hauckcarola developmentofanautomatedmanufacturingprocessforlargescaleproductionofautologoustcelltherapies
AT gerstmayerbernhard developmentofanautomatedmanufacturingprocessforlargescaleproductionofautologoustcelltherapies
AT webersilvio developmentofanautomatedmanufacturingprocessforlargescaleproductionofautologoustcelltherapies
AT kirkpatrickaileen developmentofanautomatedmanufacturingprocessforlargescaleproductionofautologoustcelltherapies