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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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2022
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
Descripción
Sumario: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.