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Vero cell upstream bioprocess development for the production of viral vectors and vaccines
The Vero cell line is considered the most used continuous cell line for the production of viral vectors and vaccines. Historically, it is the first cell line that was approved by the WHO for the production of human vaccines. Comprehensive experimental data on the production of many viruses using the...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Authors. Published by Elsevier Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7405825/ https://www.ncbi.nlm.nih.gov/pubmed/32768520 http://dx.doi.org/10.1016/j.biotechadv.2020.107608 |
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author | Kiesslich, Sascha Kamen, Amine A. |
author_facet | Kiesslich, Sascha Kamen, Amine A. |
author_sort | Kiesslich, Sascha |
collection | PubMed |
description | The Vero cell line is considered the most used continuous cell line for the production of viral vectors and vaccines. Historically, it is the first cell line that was approved by the WHO for the production of human vaccines. Comprehensive experimental data on the production of many viruses using the Vero cell line can be found in the literature. However, the vast majority of these processes is relying on the microcarrier technology. While this system is established for the large-scale manufacturing of viral vaccine, it is still quite complex and labor intensive. Moreover, scale-up remains difficult and is limited by the surface area given by the carriers. To overcome these and other drawbacks and to establish more efficient manufacturing processes, it is a priority to further develop the Vero cell platform by applying novel bioprocess technologies. Especially in times like the current COVID-19 pandemic, advanced and scalable platform technologies could provide more efficient and cost-effective solutions to meet the global vaccine demand. Herein, we review the prevailing literature on Vero cell bioprocess development for the production of viral vectors and vaccines with the aim to assess the recent advances in bioprocess development. We critically underline the need for further research activities and describe bottlenecks to improve the Vero cell platform by taking advantage of recent developments in the cell culture engineering field. |
format | Online Article Text |
id | pubmed-7405825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Authors. Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74058252020-08-05 Vero cell upstream bioprocess development for the production of viral vectors and vaccines Kiesslich, Sascha Kamen, Amine A. Biotechnol Adv Research Review Paper The Vero cell line is considered the most used continuous cell line for the production of viral vectors and vaccines. Historically, it is the first cell line that was approved by the WHO for the production of human vaccines. Comprehensive experimental data on the production of many viruses using the Vero cell line can be found in the literature. However, the vast majority of these processes is relying on the microcarrier technology. While this system is established for the large-scale manufacturing of viral vaccine, it is still quite complex and labor intensive. Moreover, scale-up remains difficult and is limited by the surface area given by the carriers. To overcome these and other drawbacks and to establish more efficient manufacturing processes, it is a priority to further develop the Vero cell platform by applying novel bioprocess technologies. Especially in times like the current COVID-19 pandemic, advanced and scalable platform technologies could provide more efficient and cost-effective solutions to meet the global vaccine demand. Herein, we review the prevailing literature on Vero cell bioprocess development for the production of viral vectors and vaccines with the aim to assess the recent advances in bioprocess development. We critically underline the need for further research activities and describe bottlenecks to improve the Vero cell platform by taking advantage of recent developments in the cell culture engineering field. The Authors. Published by Elsevier Inc. 2020-11-15 2020-08-05 /pmc/articles/PMC7405825/ /pubmed/32768520 http://dx.doi.org/10.1016/j.biotechadv.2020.107608 Text en © 2020 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Research Review Paper Kiesslich, Sascha Kamen, Amine A. Vero cell upstream bioprocess development for the production of viral vectors and vaccines |
title | Vero cell upstream bioprocess development for the production of viral vectors and vaccines |
title_full | Vero cell upstream bioprocess development for the production of viral vectors and vaccines |
title_fullStr | Vero cell upstream bioprocess development for the production of viral vectors and vaccines |
title_full_unstemmed | Vero cell upstream bioprocess development for the production of viral vectors and vaccines |
title_short | Vero cell upstream bioprocess development for the production of viral vectors and vaccines |
title_sort | vero cell upstream bioprocess development for the production of viral vectors and vaccines |
topic | Research Review Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7405825/ https://www.ncbi.nlm.nih.gov/pubmed/32768520 http://dx.doi.org/10.1016/j.biotechadv.2020.107608 |
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