McCarron Alexandra, Donnelley Martin, McIntyre Chantelle, Parsons David
1 Adelaide Medical School, SA Pathology, Women's and Children's Hospital, Adelaide, Australia.
2 Robinson Research Institute, The University of Adelaide, Adelaide, Australia.
Hum Gene Ther Methods. 2019 Jun;30(3):93-101. doi: 10.1089/hgtb.2019.038. Epub 2019 Jun 5.
Scalable lentiviral vector (LV) manufacturing is vital for successful commercialization of LV-based gene and cell therapy products. Accordingly, efforts are currently focused on developing and adapting technologies to address both upstream and downstream production bottlenecks. To overcome the limitations of current upstream processes, researchers are now favoring the use of bioreactors over traditional two-dimensional culture platforms. Bioreactors provide many advantages for manufacturing biomolecules, including process automation, tight regulation of production conditions, reduced labor input, and higher productivity potential. This study describes a transient LV production strategy employing a single-use, packed-bed bioreactor vessel. Functional LV titers in the 10 TU/mL range were achieved, and after concentration yields of up to 10 TU/mL were attained. This proof of principle study demonstrates that LV can be successfully produced in a packed-bed system. With further optimization, a packed-bed bioreactor could offer a potential scale-out solution for LV manufacturing.
可扩展的慢病毒载体(LV)生产对于基于LV的基因和细胞治疗产品的成功商业化至关重要。因此,目前的工作重点是开发和应用技术来解决上游和下游生产瓶颈。为了克服当前上游工艺的局限性,研究人员现在更倾向于使用生物反应器而非传统的二维培养平台。生物反应器在生物分子生产方面具有许多优势,包括工艺自动化、生产条件的严格调控、劳动力投入减少以及更高的生产潜力。本研究描述了一种采用一次性填充床生物反应器容器的瞬时LV生产策略。实现了10 TU/mL范围内的功能性LV滴度,浓缩后产量高达10 TU/mL。这项原理验证研究表明LV可以在填充床系统中成功生产。通过进一步优化,填充床生物反应器可为LV生产提供潜在的扩大规模解决方案。