Tran Michelle Yen, Kamen Amine A
Viral Vectors and Vaccines Bioprocessing Group, Bioengineering Department, McGill University, Montreal, QC, Canada.
Front Bioeng Biotechnol. 2022 Jun 14;10:887716. doi: 10.3389/fbioe.2022.887716. eCollection 2022.
The field of lentiviral vector (LV) production continues to face challenges in large-scale manufacturing, specifically regarding producing enough vectors to meet the demand for treating patients as well as producing high and consistent quality of vectors for efficient dosing. Two areas of interest are the use of stable producer cell lines, which facilitates the scalability of LV production processes as well as making the process more reproducible and robust for clinical applications, and the search of a cell retention device scalable to industrial-size bioreactors. This manuscript investigates a stable producer cell line for producing LVs with GFP as the transgene at shake flask scale and demonstrates LV production at 3L bioreactor scale using the Tangential Flow Depth Filtration (TFDF) as a cell retention device in perfusion mode. Cumulative functional yields of 3.3 x 10 and 3.9 x 10 transducing units were achieved; the former over 6 days of LV production with 16.3 L of perfused media and the latter over 4 days with 16 L. In comparing to a previously published value that was achieved using the same stable producer cell line and the acoustic filter as the perfusion device at the same bioreactor scale, the TFDF perfusion run produced 1.5-fold higher cumulative functional yield. Given its scale-up potential, the TFDF is an excellent candidate to be further evaluated to determine optimized conditions that can ultimately support continuous manufacturing of LVs at large scale.
慢病毒载体(LV)生产领域在大规模制造方面仍面临挑战,特别是在生产足够数量的载体以满足患者治疗需求以及生产高质量且稳定一致的载体以实现有效给药方面。有两个感兴趣的领域,一是使用稳定的生产细胞系,这有助于提高LV生产过程的可扩展性,并使该过程在临床应用中更具可重复性和稳健性;另一个是寻找一种可扩展至工业规模生物反应器的细胞截留装置。本手稿研究了一种在摇瓶规模下生产以绿色荧光蛋白(GFP)作为转基因的LV的稳定生产细胞系,并展示了在3L生物反应器规模下使用切向流深度过滤(TFDF)作为灌注模式下的细胞截留装置生产LV。分别实现了3.3×10和3.9×10转导单位的累积功能产量;前者在6天的LV生产过程中使用16.3L灌注培养基,后者在4天内使用16L。与之前发表的在相同生物反应器规模下使用相同稳定生产细胞系和声学过滤器作为灌注装置所获得的值相比,TFDF灌注运行产生的累积功能产量高出1.5倍。鉴于其放大潜力,TFDF是一个很好的候选对象,有待进一步评估以确定最终能够支持大规模连续生产LV的优化条件。