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无血清 Vero 细胞生产平台用于生产嵌合病毒候选疫苗。

A serum-free Vero production platform for a chimeric virus vaccine candidate.

机构信息

MedImmune Vaccines, Inc., 3055 Patrick Henry Drive, Santa Clara, CA, 95054, USA,

出版信息

Cytotechnology. 2006 Jul;51(3):183-92. doi: 10.1007/s10616-006-9030-7. Epub 2006 Nov 16.

Abstract

MedImmune Vaccines has engineered a live, attenuated chimeric virus that could prevent infections caused by parainfluenza virus type 3 (PIV3) and respiratory syncytial virus (RSV), causative agents of acute respiratory diseases in infants and young children. The work here details the development of a serum-free Vero cell culture production platform for this virus vaccine candidate. Efforts to identify critical process parameters and optimize culture conditions increased infectious virus titers by approximately 2 log(10) TCID(50)/ml over the original serum-free process. In particular, the addition of a chemically defined lipid concentrate to the pre-infection medium along with the shift to a lower post-infection cultivation temperature increased virus titers by almost 100-fold. This improved serum-free process achieved comparable virus titers to the serum-supplemented process, and demonstrated consistent results upon scale-up: Vero cultures in roller bottles, spinner flasks and bioreactors reproducibly generated maximum infectious virus titers of 8 log(10) TCID(50)/ml.

摘要

美迪默生疫苗公司(MedImmune Vaccines)研发出一种活的、减毒嵌合病毒,可预防副流感病毒 3 型(PIV3)和呼吸道合胞病毒(RSV)引起的感染,这两种病毒是婴幼儿急性呼吸道疾病的病原体。本工作详细介绍了该病毒候选疫苗的无血清 Vero 细胞培养生产平台的开发。通过鉴定关键工艺参数和优化培养条件,与原始无血清工艺相比,感染性病毒滴度提高了约 2 个对数(10)TCID(50)/ml。特别是,在感染前培养基中添加化学定义的脂质浓缩物,并将培养温度降低到更低的水平,可将病毒滴度提高近 100 倍。该改进的无血清工艺达到了与补充血清的工艺相当的病毒滴度,并在放大规模时显示出一致的结果:在滚瓶、搅拌瓶和生物反应器中的 Vero 培养物可重复性地产生最大感染性病毒滴度为 8 对数(10)TCID(50)/ml。

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