维罗细胞
病毒学
微载波
病毒
生物反应器
生物
水泡性口炎病毒
冠状病毒
微生物学
2019年冠状病毒病(COVID-19)
细胞培养
医学
传染病(医学专业)
疾病
植物
病理
遗传学
作者
Christopher Ton,Victoria Stabile,Elizabeth J. Carey,Adam Maraikar,Travis Whitmer,Samantha Marrone,Nelson Lee Afanador,Igor Zabrodin,Greeshma Manomohan,Melissa C. Whiteman,Carl Hofmann
标识
DOI:10.1016/j.btre.2023.e00782
摘要
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.
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