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Bioreactor production of rVSV‐based vectors in Vero cell suspension cultures
The Vero cell line is the most used continuous cell line in viral vaccine manufacturing. This adherent cell culture platform requires the use of surfaces to support cell growth, typically roller bottles, or microcarriers. We have recently compared the production of rVSV‐ZEBOV on Vero cells between m...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8252067/ https://www.ncbi.nlm.nih.gov/pubmed/33837958 http://dx.doi.org/10.1002/bit.27785 |
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author | Kiesslich, Sascha Kim, Gyoung N. Shen, Chun F. Kang, C. Yong Kamen, Amine A. |
author_facet | Kiesslich, Sascha Kim, Gyoung N. Shen, Chun F. Kang, C. Yong Kamen, Amine A. |
author_sort | Kiesslich, Sascha |
collection | PubMed |
description | The Vero cell line is the most used continuous cell line in viral vaccine manufacturing. This adherent cell culture platform requires the use of surfaces to support cell growth, typically roller bottles, or microcarriers. We have recently compared the production of rVSV‐ZEBOV on Vero cells between microcarrier and fixed‐bed bioreactors. However, suspension cultures are considered superior with regard to process scalability. Therefore, we further explore the Vero suspension system for recombinant vesicular stomatitis virus (rVSV)‐vectored vaccine production. Previously, this suspension cell line was only able to be cultivated in a proprietary medium. Here, we expand the adaptation and bioreactor cultivation to a serum‐free commercial medium. Following small‐scale optimization and screening studies, we demonstrate bioreactor productions of highly relevant vaccines and vaccine candidates against Ebola virus disease, HIV, and coronavirus disease 2019 in the Vero suspension system. rVSV‐ZEBOV, rVSV‐HIV, and rVSV(Ind)‐msp‐S(F)‐Gtc can replicate to high titers in the bioreactor, reaching 3.87 × 10(7) TCID(50)/ml, 2.12 × 10(7) TCID(50)/ml, and 3.59 × 10(9) TCID(50)/ml, respectively. Furthermore, we compare cell‐specific productivities, and the quality of the produced viruses by determining the ratio of total viral particles to infectious viral particles. |
format | Online Article Text |
id | pubmed-8252067 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82520672021-07-07 Bioreactor production of rVSV‐based vectors in Vero cell suspension cultures Kiesslich, Sascha Kim, Gyoung N. Shen, Chun F. Kang, C. Yong Kamen, Amine A. Biotechnol Bioeng ARTICLES The Vero cell line is the most used continuous cell line in viral vaccine manufacturing. This adherent cell culture platform requires the use of surfaces to support cell growth, typically roller bottles, or microcarriers. We have recently compared the production of rVSV‐ZEBOV on Vero cells between microcarrier and fixed‐bed bioreactors. However, suspension cultures are considered superior with regard to process scalability. Therefore, we further explore the Vero suspension system for recombinant vesicular stomatitis virus (rVSV)‐vectored vaccine production. Previously, this suspension cell line was only able to be cultivated in a proprietary medium. Here, we expand the adaptation and bioreactor cultivation to a serum‐free commercial medium. Following small‐scale optimization and screening studies, we demonstrate bioreactor productions of highly relevant vaccines and vaccine candidates against Ebola virus disease, HIV, and coronavirus disease 2019 in the Vero suspension system. rVSV‐ZEBOV, rVSV‐HIV, and rVSV(Ind)‐msp‐S(F)‐Gtc can replicate to high titers in the bioreactor, reaching 3.87 × 10(7) TCID(50)/ml, 2.12 × 10(7) TCID(50)/ml, and 3.59 × 10(9) TCID(50)/ml, respectively. Furthermore, we compare cell‐specific productivities, and the quality of the produced viruses by determining the ratio of total viral particles to infectious viral particles. John Wiley and Sons Inc. 2021-05-05 2021-07 /pmc/articles/PMC8252067/ /pubmed/33837958 http://dx.doi.org/10.1002/bit.27785 Text en © 2021 The Authors. Biotechnology and Bioengineering published by Wiley Periodicals LLC https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | ARTICLES Kiesslich, Sascha Kim, Gyoung N. Shen, Chun F. Kang, C. Yong Kamen, Amine A. Bioreactor production of rVSV‐based vectors in Vero cell suspension cultures |
title | Bioreactor production of rVSV‐based vectors in Vero cell suspension cultures |
title_full | Bioreactor production of rVSV‐based vectors in Vero cell suspension cultures |
title_fullStr | Bioreactor production of rVSV‐based vectors in Vero cell suspension cultures |
title_full_unstemmed | Bioreactor production of rVSV‐based vectors in Vero cell suspension cultures |
title_short | Bioreactor production of rVSV‐based vectors in Vero cell suspension cultures |
title_sort | bioreactor production of rvsv‐based vectors in vero cell suspension cultures |
topic | ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8252067/ https://www.ncbi.nlm.nih.gov/pubmed/33837958 http://dx.doi.org/10.1002/bit.27785 |
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