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用 Ambr15 系统优化 VSV-ΔG-spike 生产工艺,用于 SARS-COV-2 疫苗。

Optimization of VSV-ΔG-spike production process with the Ambr15 system for a SARS-COV-2 vaccine.

机构信息

Department of Biotechnology, Israel Institute for Biological, Chemical and Environmental Sciences, Ness Ziona, Israel.

Department of Organic Chemistry, Israel Institute for Biological, Chemical and Environmental Sciences, Ness Ziona, Israel.

出版信息

Biotechnol Bioeng. 2022 Jul;119(7):1839-1848. doi: 10.1002/bit.28088. Epub 2022 Mar 31.

DOI:10.1002/bit.28088
PMID:35319097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9082513/
Abstract

To face the coronavirus disease 2019 pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus, our institute has developed the rVSV-ΔG-spike vaccine, in which the glycoprotein of vesicular stomatitis virus (VSV) was replaced by the spike protein of SARS-CoV-2. Many process parameters can influence production yield. To maximize virus vaccine yield, each parameter should be tested independently and in combination with others. Here, we report the optimization of the production of the VSV-ΔG-spike vaccine in Vero cells using the Ambr15 system. This system facilitates high-throughput screening of process parameters, as it contains 24 individually controlled, single-use stirred-tank minireactors. During optimization, critical parameters were tested. Those parameters included: cell densities; the multiplicity of infection; virus production temperature; medium addition and medium exchange; and supplementation of glucose in the virus production step. Virus production temperature, medium addition, and medium exchange were all found to significantly influence the yield. The optimized parameters were tested in the BioBLU 5p bioreactors production process and those that were found to contribute to the vaccine yield were integrated into the final process. The findings of this study demonstrate that an Ambr15 system is an effective tool for bioprocess optimization of vaccine production using macrocarriers and that the combination of production temperature, rate of medium addition, and medium exchange significantly improved virus yield.

摘要

为应对由严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)病毒引起的 2019 年冠状病毒病,我们研究所开发了 rVSV-ΔG-刺突疫苗,其中水疱性口炎病毒(VSV)的糖蛋白被 SARS-CoV-2 的刺突蛋白取代。许多工艺参数会影响生产产量。为了使病毒疫苗产量最大化,每个参数都应单独进行测试,并与其他参数进行组合测试。在这里,我们报告了使用 Ambr15 系统在 Vero 细胞中生产 VSV-ΔG-刺突疫苗的优化。该系统便于高通量筛选工艺参数,因为它包含 24 个单独控制的、一次性使用的搅拌槽微型反应器。在优化过程中,对关键参数进行了测试。这些参数包括:细胞密度;感染复数;病毒生产温度;培养基添加和培养基交换;以及在病毒生产步骤中补充葡萄糖。病毒生产温度、培养基添加和培养基交换均显著影响产量。优化后的参数在 BioBLU 5p 生物反应器生产过程中进行了测试,并将有助于疫苗产量的参数整合到最终工艺中。本研究的结果表明,Ambr15 系统是使用大载体优化疫苗生产生物工艺的有效工具,生产温度、培养基添加率和培养基交换的组合显著提高了病毒产量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fa/9082513/9ea2f62f298f/BIT-119-1839-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fa/9082513/50fd63bea9a0/BIT-119-1839-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fa/9082513/27e6a7bf1843/BIT-119-1839-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fa/9082513/885313837925/BIT-119-1839-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fa/9082513/0daf9dac74de/BIT-119-1839-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fa/9082513/4bc319605608/BIT-119-1839-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fa/9082513/9ea2f62f298f/BIT-119-1839-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fa/9082513/50fd63bea9a0/BIT-119-1839-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fa/9082513/27e6a7bf1843/BIT-119-1839-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fa/9082513/885313837925/BIT-119-1839-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fa/9082513/0daf9dac74de/BIT-119-1839-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fa/9082513/4bc319605608/BIT-119-1839-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fa/9082513/9ea2f62f298f/BIT-119-1839-g003.jpg

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