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
Autolus Limited, The MediaWorks, 191 Wood Lane, London W12 7FP, UK.
Cell and Gene Therapy, Kings (CGT-K), King's College London, London SE5 9NU, UK.
Mol Ther Methods Clin Dev. 2022 Dec 9;28:116-128. doi: 10.1016/j.omtm.2022.12.006. eCollection 2023 Mar 9.
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 10-10 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.
γ-逆转录病毒载体(γ-RV)是基因治疗应用中的强大工具。目前的临床载体由稳定的生产细胞系产生,所需的进一步下游处理最少,而通过瞬时转染产生的γ-RV的纯化方案尚未得到充分研究。我们旨在开发一种纯化瞬时产生的γ-RV的方法,用于早期临床研究。在此,我们报告了一种通过高速离心对临床应用中瞬时转染产生的γ-RV进行一步纯化的简单方法。高速离心能够将病毒滴度浓缩至10-10 TU/mL范围,总体回收率>80%。对研究级浓缩载体的分析表明,产品和工艺相关杂质有足够的减少。此外,BioReliance对临床级γ-RV的产品表征显示,与监管机构批准的临床应用稳定生产细胞系载体相比,每个转导单位的杂质低两个对数。在CAR T细胞制造方面,通过瞬时转染产生并通过高速离心纯化的临床级γ-RV与临床级稳定生产细胞系产生的γ-RV相似。这种方法对于使用γ-RV在早期和晚期临床试验之间建立载体供应的研究具有价值。