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Efficient clinical-grade γ-retroviral vector purification by high-speed centrifugation for CAR T cell manufacturing
γ-Retroviral vectors (γ-RV) are powerful tools for gene therapy applications. Current clinical vectors are produced from stable producer cell lines which require minimal further downstream processing, while purification schemes for γ-RV produced by transient transfection have not been thoroughly inv...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9808014/ https://www.ncbi.nlm.nih.gov/pubmed/36620071 http://dx.doi.org/10.1016/j.omtm.2022.12.006 |
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author | Mekkaoui, Leila Tejerizo, Jose G. Abreu, Sara Rubat, Lydie Nikoniuk, Aleksandra Macmorland, William Horlock, Claire Matsumoto, Sofia Williams, Sarah Smith, Koval Price, Juliet Srivastava, Saket Hussain, Rehan Banani, Mohammad Amin Day, William Stevenson, Elena Madigan, Meghan Chen, Jie Khinder, Ravin Miah, Shahed Walker, Simon Ade-Onojobi, Michael Domining, Sabine Sillibourne, James Sabatino, Marianna Slepushkin, Vladimir Farzaneh, Farzin Pule, Martin |
author_facet | Mekkaoui, Leila Tejerizo, Jose G. Abreu, Sara Rubat, Lydie Nikoniuk, Aleksandra Macmorland, William Horlock, Claire Matsumoto, Sofia Williams, Sarah Smith, Koval Price, Juliet Srivastava, Saket Hussain, Rehan Banani, Mohammad Amin Day, William Stevenson, Elena Madigan, Meghan Chen, Jie Khinder, Ravin Miah, Shahed Walker, Simon Ade-Onojobi, Michael Domining, Sabine Sillibourne, James Sabatino, Marianna Slepushkin, Vladimir Farzaneh, Farzin Pule, Martin |
author_sort | Mekkaoui, Leila |
collection | PubMed |
description | γ-Retroviral vectors (γ-RV) are powerful tools for gene therapy applications. Current clinical vectors are produced from stable producer cell lines which require minimal further downstream processing, while purification schemes for γ-RV produced by transient transfection have not been thoroughly investigated. We aimed to develop a method to purify transiently produced γ-RV for early clinical studies. Here, we report a simple one-step purification method by high-speed centrifugation for γ-RV produced by transient transfection for clinical application. High-speed centrifugation enabled the concentration of viral titers in the range of 10(7)–10(8) TU/mL with >80% overall recovery. Analysis of research-grade concentrated vector revealed sufficient reduction in product- and process-related impurities. Furthermore, product characterization of clinical-grade γ-RV by BioReliance demonstrated two-logs lower impurities per transducing unit compared with regulatory authority-approved stable producer cell line vector for clinical application. In terms of CAR T cell manufacturing, clinical-grade γ-RV produced by transient transfection and purified by high-speed centrifugation was similar to γ-RV produced from a clinical-grade stable producer cell line. This method will be of value for studies using γ-RV to bridge vector supply between early- and late-stage clinical trials. |
format | Online Article Text |
id | pubmed-9808014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-98080142023-01-05 Efficient clinical-grade γ-retroviral vector purification by high-speed centrifugation for CAR T cell manufacturing Mekkaoui, Leila Tejerizo, Jose G. Abreu, Sara Rubat, Lydie Nikoniuk, Aleksandra Macmorland, William Horlock, Claire Matsumoto, Sofia Williams, Sarah Smith, Koval Price, Juliet Srivastava, Saket Hussain, Rehan Banani, Mohammad Amin Day, William Stevenson, Elena Madigan, Meghan Chen, Jie Khinder, Ravin Miah, Shahed Walker, Simon Ade-Onojobi, Michael Domining, Sabine Sillibourne, James Sabatino, Marianna Slepushkin, Vladimir Farzaneh, Farzin Pule, Martin Mol Ther Methods Clin Dev Original Article γ-Retroviral vectors (γ-RV) are powerful tools for gene therapy applications. Current clinical vectors are produced from stable producer cell lines which require minimal further downstream processing, while purification schemes for γ-RV produced by transient transfection have not been thoroughly investigated. We aimed to develop a method to purify transiently produced γ-RV for early clinical studies. Here, we report a simple one-step purification method by high-speed centrifugation for γ-RV produced by transient transfection for clinical application. High-speed centrifugation enabled the concentration of viral titers in the range of 10(7)–10(8) TU/mL with >80% overall recovery. Analysis of research-grade concentrated vector revealed sufficient reduction in product- and process-related impurities. Furthermore, product characterization of clinical-grade γ-RV by BioReliance demonstrated two-logs lower impurities per transducing unit compared with regulatory authority-approved stable producer cell line vector for clinical application. In terms of CAR T cell manufacturing, clinical-grade γ-RV produced by transient transfection and purified by high-speed centrifugation was similar to γ-RV produced from a clinical-grade stable producer cell line. This method will be of value for studies using γ-RV to bridge vector supply between early- and late-stage clinical trials. American Society of Gene & Cell Therapy 2022-12-09 /pmc/articles/PMC9808014/ /pubmed/36620071 http://dx.doi.org/10.1016/j.omtm.2022.12.006 Text en © 2022 The Authors 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 Mekkaoui, Leila Tejerizo, Jose G. Abreu, Sara Rubat, Lydie Nikoniuk, Aleksandra Macmorland, William Horlock, Claire Matsumoto, Sofia Williams, Sarah Smith, Koval Price, Juliet Srivastava, Saket Hussain, Rehan Banani, Mohammad Amin Day, William Stevenson, Elena Madigan, Meghan Chen, Jie Khinder, Ravin Miah, Shahed Walker, Simon Ade-Onojobi, Michael Domining, Sabine Sillibourne, James Sabatino, Marianna Slepushkin, Vladimir Farzaneh, Farzin Pule, Martin Efficient clinical-grade γ-retroviral vector purification by high-speed centrifugation for CAR T cell manufacturing |
title | Efficient clinical-grade γ-retroviral vector purification by high-speed centrifugation for CAR T cell manufacturing |
title_full | Efficient clinical-grade γ-retroviral vector purification by high-speed centrifugation for CAR T cell manufacturing |
title_fullStr | Efficient clinical-grade γ-retroviral vector purification by high-speed centrifugation for CAR T cell manufacturing |
title_full_unstemmed | Efficient clinical-grade γ-retroviral vector purification by high-speed centrifugation for CAR T cell manufacturing |
title_short | Efficient clinical-grade γ-retroviral vector purification by high-speed centrifugation for CAR T cell manufacturing |
title_sort | efficient clinical-grade γ-retroviral vector purification by high-speed centrifugation for car t cell manufacturing |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9808014/ https://www.ncbi.nlm.nih.gov/pubmed/36620071 http://dx.doi.org/10.1016/j.omtm.2022.12.006 |
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