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使用一次性生物反应器开发和扩大重组水疱性口炎病毒载体新冠病毒疫苗的生产工艺

Development and scale-up of rVSV-SARS-CoV-2 vaccine process using single use bioreactor.

作者信息

Ton Christopher, Stabile Victoria, Carey Elizabeth, Maraikar Adam, Whitmer Travis, Marrone Samantha, Afanador Nelson Lee, Zabrodin Igor, Manomohan Greeshma, Whiteman Melissa, Hofmann Carl

机构信息

Vaccine Process Development, Merck & Co., Inc., West Point, Pennsylvania, 19486, United States.

Bioprocess Clinical Manufacturing & Technology, Merck & Co., Inc., West Point, Pennsylvania, 19486, United States.

出版信息

Biotechnol Rep (Amst). 2023 Mar;37:e00782. doi: 10.1016/j.btre.2023.e00782. Epub 2023 Jan 16.

Abstract

The outbreak of the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that causes the Coronavirus Disease 2019 (COVID-19) has spread through the globe at an alarming speed. The disease has become a global pandemic affecting millions of people and created public health crises worldwide. Among many efforts to urgently develop a vaccine against this disease, we developed an industrial-scale closed, single use manufacturing process for V590, a vaccine candidate for SARS-CoV-2. V590 is a recombinant vesicular stomatitis virus (rVSV) genetically engineered to express SARS-CoV-2 glycoprotein. In this work, we describe the development and optimization of serum-free microcarrier production of V590 in Vero cells in a closed system. To achieve the maximum virus productivity, we optimized pH and temperature during virus production in 3 liters (L) bioreactors. Virus productivity was improved (by ∼1 log) by using pH 7.0 and temperature at 34.0 °C. The optimal production condition was successfully scaled up to a 2000 L Single Use Bioreactor (SUB), producing a maximum virus titer of ∼1.0e+7 plaque forming units (PFU)/mL. Further process intensification and simplification, including growing Vero cells at 2 gs per liter (g/L) of Cytodex-1 Gamma microcarriers and eliminating the media exchange (MX) step prior to infection helped to increase virus productivity by ∼2-fold.

摘要

导致2019冠状病毒病(COVID-19)的新型严重急性呼吸综合征冠状病毒2(SARS-CoV-2)疫情已以惊人的速度在全球蔓延。该疾病已成为一场全球大流行,影响了数百万人,并在全球范围内引发了公共卫生危机。在众多迫切研发针对该疾病疫苗的努力中,我们为SARS-CoV-2疫苗候选物V590开发了一种工业规模的封闭式一次性生产工艺。V590是一种经过基因工程改造以表达SARS-CoV-2糖蛋白的重组水疱性口炎病毒(rVSV)。在这项工作中,我们描述了在封闭系统中Vero细胞无血清微载体生产V590的工艺开发和优化。为了实现最大病毒生产力,我们在3升(L)生物反应器中生产病毒期间优化了pH值和温度。通过使用pH 7.0和34.0°C的温度,病毒生产力提高了(约1个对数)。最佳生产条件成功扩大到2000 L一次性生物反应器(SUB),产生的最大病毒滴度约为1.0e+7空斑形成单位(PFU)/mL。进一步的工艺强化和简化,包括以每升(g/L)Cytodex-1 Gamma微载体2 g的浓度培养Vero细胞以及在感染前消除培养基更换(MX)步骤,有助于将病毒生产力提高约2倍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4890/9869428/e560c25e303c/gr1a.jpg

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