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在可扩展的高细胞密度生物反应器中生产严重急性呼吸综合征冠状病毒2

SARS-CoV-2 Production in a Scalable High Cell Density Bioreactor.

作者信息

Offersgaard Anna, Duarte Hernandez Carlos Rene, Pihl Anne Finne, Costa Rui, Venkatesan Nandini Prabhakar, Lin Xiangliang, Van Pham Long, Feng Shan, Fahnøe Ulrik, Scheel Troels Kasper Høyer, Ramirez Santseharay, Reichl Udo, Bukh Jens, Genzel Yvonne, Gottwein Judith Margarete

机构信息

Copenhagen Hepatitis C Program (CO-HEP), Department of Infectious Diseases, Copenhagen University Hospital-Hvidovre, 2650 Hvidovre, Denmark.

Copenhagen Hepatitis C Program (CO-HEP), Department of Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.

出版信息

Vaccines (Basel). 2021 Jun 29;9(7):706. doi: 10.3390/vaccines9070706.

Abstract

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has demonstrated the value of pursuing different vaccine strategies. Vaccines based on whole viruses, a widely used vaccine technology, depend on efficient virus production. This study aimed to establish SARS-CoV-2 production in the scalable packed-bed CelCradle 500-AP bioreactor. CelCradle 500-AP bottles with 0.5 L working volume and 5.5 g BioNOC™ II carriers were seeded with 1.5 × 10 Vero (WHO) cells, approved for vaccine production, in animal component-free medium and infected at a multiplicity of infection of 0.006 at a total cell number of 2.2-2.5 × 10 cells/bottle seven days post cell seeding. Among several tested conditions, two harvests per day and a virus production temperature of 33 °C resulted in the highest virus yield with a peak SARS-CoV-2 infectivity titer of 7.3 log 50% tissue culture infectious dose (TCID)/mL at 72 h post-infection. Six harvests had titers of ≥6.5 log TCID/mL, and a total of 10.5 log TCID were produced in ~5 L. While trypsin was reported to enhance virus spread in cell culture, addition of 0.5% recombinant trypsin after infection did not improve virus yields. Overall, we demonstrated successful animal component-free production of SARS-CoV-2 in well-characterized Vero (WHO) cells in a scalable packed-bed bioreactor.

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)大流行已证明采用不同疫苗策略的价值。基于全病毒的疫苗是一种广泛使用的疫苗技术,依赖于高效的病毒生产。本研究旨在利用可扩展的填充床CelCradle 500-AP生物反应器生产SARS-CoV-2。将工作体积为0.5 L且装有5.5 g BioNOC™ II载体的CelCradle 500-AP瓶接种1.5×10个经批准用于疫苗生产的Vero(世卫组织)细胞,置于无动物成分的培养基中,并在细胞接种后7天,以感染复数0.006进行感染,每瓶总细胞数为2.2 - 2.5×10个细胞。在几个测试条件中,每天收获两次且病毒生产温度为33°C时,病毒产量最高,感染后72小时SARS-CoV-2感染性滴度峰值为7.3 log 50%组织培养感染剂量(TCID)/mL。六次收获的滴度≥6.5 log TCID/mL,在约5 L体积中总共产生了10.5 log TCID。虽然据报道胰蛋白酶可增强病毒在细胞培养中的传播,但感染后添加0.5%重组胰蛋白酶并未提高病毒产量。总体而言,我们证明了在可扩展的填充床生物反应器中,在特性明确的Vero(世卫组织)细胞中成功实现了无动物成分的SARS-CoV-2生产。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/047e/8310283/abb0d62c21b0/vaccines-09-00706-g001.jpg

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