Ton Christopher, Stabile Victoria, Carey Elizabeth, Maraikar Adam, Whitmer Travis, Marrone Samantha, Afanador Nelson Lee, Zabrodin Igor, Manomohan Greeshma, Whiteman Melissa, Hofmann Carl
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.
Biotechnol Rep (Amst). 2023 Mar;37:e00782. doi: 10.1016/j.btre.2023.e00782. Epub 2023 Jan 16.
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.
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。