4.5 Article

The efficient development of a novel recombinant adenovirus zoster vaccine perfusion production process

期刊

VACCINE
卷 40, 期 13, 页码 2036-2043

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.vaccine.2022.02.024

关键词

HEK 293 cells; Adenovirus; Zoster vaccine; Perfusion cultivation; Process optimization

资金

  1. National Key Research and Development Program of China,China [2018YFA0900804]
  2. National Natural Science Foundation of China, China [22108100]
  3. Natural Science Foundation of Jiangsu Province, China [BK20210472]
  4. national first-class discipline program of Light Industry Technology and Engineering, China [LITE2018-24]

向作者/读者索取更多资源

The perfusion process is an optimized strategy for the production of adenovirus vector vaccines, and it is of great importance for efficient vaccine production.
The adenovirus vector vaccines induce humoral and cellular immune responses and have been used to develop vaccines for effective prevention of life-threating viruses, such as Ebola and Coronaviruses. High demand of vaccines worldwide requires optimization of the production process. Perfusion process increases cell concentration and volumetric productivity, so that it becomes the commonly used strategy in vaccine production In this study, we optimized and developed a perfusion process for the adenovirus-based zoster vaccine production efficiently. We first tested different perfusion strategies in shake flasks, showing semi-continuous strategies for optimal HEK 293 cell growth. We then evaluated three empirical key process parameters (cell concentration at the time of infection (VCC), multiplicity of infection (MOI), virus production pH) by the design of experiment (DoE) method, from which the robust setpoint (VCC 1.04 x 10(7) cells/mL, MOI 9, and virus production pH 7.17) was confirmed in both shake flask and 2 L benchtop bioreactor. In the bioreactor, we compared the performances of two perfusion systems, the commercially-available XCell ATF (R) system and a novel peristaltic pump-driven alternating tangential flow perfusion system (PATFP system) that we developed. During cell cultivation stage, both perfusion systems have comparable performances regarding viable cell concentration and cell viability. At 2 dpi, the PATFP system resulted in an adenovirus titer of 2.1 x 10(10) IFU/mL and cell-specific virus yield of 2,062 IFU/cell, reaching 75% and 77% of values for XCell ATF (R) system. This study demonstrates the perfusion process to be superior strategy for adenovirus-based vaccine production compared to the batch-mode strategy (1,467 IFU/cell). Furthermore, our PATFP system shows potential to be comparable to the XCell ATF (R) system, and it would become an alternative perfusion strategy for the vaccine production. (C) 2022 Elsevier Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据