Tona Robert M, Shah Reeti, Middaugh Kimberly, Steve Justin, Marques João, Roszell Blair R, Jung Cindy
Cell and Gene Therapy, GSK, 1250 S. Collegeville Road, Collegeville, PA 19426, USA.
CMC Analytical, GSK, 1250 S. Collegeville Road, Collegeville, PA 19426, USA.
Mol Ther Methods Clin Dev. 2023 Mar 3;29:93-107. doi: 10.1016/j.omtm.2023.02.017. eCollection 2023 Jun 8.
For gene therapies to become more accessible and affordable treatment options, process intensification is one possible strategy to increase the number of doses generated per batch of viral vector. Process intensification for lentiviral vector manufacturing can be achieved by enabling perfusion in the production bioreactor when applied in tandem with a stable producer cell line, allowing for significant expansion of cells and production of lentiviral vectors without the need for transfer plasmids. Tangential flow depth filtration was used to achieve an intensified lentiviral vector production by enabling perfusion to expand cell density and allow for continuous separation of lentiviral vectors from producer cells. Hollow-fiber depth filters made of polypropylene with 2- to 4-μm channels demonstrated high filter capacity, extended functional life, and efficient separation of lentiviral vectors from producer cells and debris when used for this intensified process. We anticipate that process intensification with tangential flow depth filtration at 200-L scale from a suspension culture can produce on the order of magnitude of 10,000 doses per batch of lentiviral vectors required for CAR T or TCR cell and gene therapy that would require approximately 2 × 10 transducing units per dose.
为了使基因疗法成为更易获得且更经济实惠的治疗选择,过程强化是增加每批病毒载体产量的一种可行策略。当与稳定的生产细胞系串联应用时,通过在生产生物反应器中实现灌注,可以实现慢病毒载体生产的过程强化,从而在无需转染质粒的情况下实现细胞的显著扩增和慢病毒载体的生产。切向流深度过滤通过实现灌注来扩大细胞密度,并允许从生产细胞中连续分离慢病毒载体,从而实现强化的慢病毒载体生产。由聚丙烯制成、通道为2至4微米的中空纤维深度过滤器在用于此强化过程时,显示出高过滤容量、延长的功能寿命以及从生产细胞和碎片中有效分离慢病毒载体的能力。我们预计,在200升规模下,通过悬浮培养进行切向流深度过滤的过程强化,每批慢病毒载体可生产约10000剂,这对于嵌合抗原受体(CAR)T细胞或T细胞受体(TCR)细胞及基因治疗而言是必需的,每剂大约需要2×10个转导单位。