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人胚肾293细胞代谢对病毒载体及疫苗生产的影响

Influence of HEK293 metabolism on the production of viral vectors and vaccine.

作者信息

Petiot Emma, Cuperlovic-Culf Miroslava, Shen Chun Fang, Kamen Amine

机构信息

Laboratoire Virologie et Pathologie Humaine (VirPath), EA4610 Université Claude Bernard Lyon 1, 7 rue guillaume paradin, 69008 Lyon, France.

Vaccine Program National Research Council, 6100 Royalmount Ave, Montreal, QC, Canada H4P 2R2.

出版信息

Vaccine. 2015 Nov 4;33(44):5974-81. doi: 10.1016/j.vaccine.2015.05.097. Epub 2015 Jun 11.

DOI:10.1016/j.vaccine.2015.05.097
PMID:26073013
Abstract

Mammalian cell cultures are increasingly used for the production of complex biopharmaceuticals including viral vectors and vaccines. HEK293 is the predominant cell line used for the transient expression of recombinant proteins and a well-established system for the production of viral vectors. Understanding metabolic requirements for high productivity in HEK293 cells remains an important area of investigation. Many authors have presented approaches for increased productivity through optimization of cellular metabolism from two distinct perspectives. One is a non-targeted approach, which is directed to improving feeding strategies by addition of exhausted or critical substrates and eventually removal of toxic metabolites. Alternatively, a targeted approach has attempted to identify specific targets for optimization through better understanding of the cellular metabolism under different operating conditions. This review will present both approaches and their successes with regards to improvement of viral production in HEK293 cells outlining the key relations between HEK293 cell metabolism and viral vector productivity. Also, we will summarize the current knowledge on HEK293 metabolism indicating remaining issues to address and problems to resolve to maximize the productivity of viral vectors in HEK293 cells.

摘要

哺乳动物细胞培养越来越多地用于生产包括病毒载体和疫苗在内的复杂生物制药产品。HEK293是用于重组蛋白瞬时表达的主要细胞系,也是生产病毒载体的成熟系统。了解HEK293细胞高产量的代谢需求仍然是一个重要的研究领域。许多作者从两个不同的角度提出了通过优化细胞代谢来提高产量的方法。一种是非靶向方法,旨在通过添加耗尽的或关键的底物来改善补料策略,并最终去除有毒代谢产物。另一种是靶向方法,试图通过更好地了解不同操作条件下的细胞代谢来确定优化的特定靶点。本综述将介绍这两种方法及其在提高HEK293细胞病毒产量方面的成功之处,概述HEK293细胞代谢与病毒载体生产力之间的关键关系。此外,我们将总结目前关于HEK293代谢的知识,指出为使HEK293细胞中病毒载体的生产力最大化而需要解决的剩余问题。

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