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High cell density perfusion process for high yield of influenza A virus production using MDCK suspension cells
ABSTRACT: Similar to the recent COVID-19 pandemic, influenza A virus poses a constant threat to the global community. For the treatment of flu disease, both antivirals and vaccines are available with vaccines the most effective and safest approach. In order to overcome limitations in egg-based vacci...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7847233/ https://www.ncbi.nlm.nih.gov/pubmed/33515287 http://dx.doi.org/10.1007/s00253-020-11050-8 |
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author | Wu, Yixiao Bissinger, Thomas Genzel, Yvonne Liu, Xuping Reichl, Udo Tan, Wen-Song |
author_facet | Wu, Yixiao Bissinger, Thomas Genzel, Yvonne Liu, Xuping Reichl, Udo Tan, Wen-Song |
author_sort | Wu, Yixiao |
collection | PubMed |
description | ABSTRACT: Similar to the recent COVID-19 pandemic, influenza A virus poses a constant threat to the global community. For the treatment of flu disease, both antivirals and vaccines are available with vaccines the most effective and safest approach. In order to overcome limitations in egg-based vaccine manufacturing, cell culture–based processes have been established. While this production method avoids egg-associated risks in face of pandemics, process intensification using animal suspension cells in high cell density perfusion cultures should allow to further increase manufacturing capacities worldwide. In this work, we demonstrate the development of a perfusion process using Madin-Darby canine kidney (MDCK) suspension cells for influenza A (H1N1) virus production from scale-down shake flask cultivations to laboratory scale stirred tank bioreactors. Shake flask cultivations using semi-perfusion mode enabled high-yield virus harvests (4.25 log(10)(HAU/100 μL)) from MDCK cells grown up to 41 × 10(6) cells/mL. Scale-up to bioreactors with an alternating tangential flow (ATF) perfusion system required optimization of pH control and implementation of a temperature shift during the infection phase. Use of a capacitance probe for on-line perfusion control allowed to minimize medium consumption. This contributed to a better process control and a more economical performance while maintaining a maximum virus titer of 4.37 log(10)(HAU/100 μL) and an infectious virus titer of 1.83 × 10(10) virions/mL. Overall, this study clearly demonstrates recent advances in cell culture–based perfusion processes for next-generation high-yield influenza vaccine manufacturing for pandemic preparedness. KEY POINTS: • First MDCK suspension cell–based perfusion process for IAV produciton was established. • “Cell density effect” was overcome and process was intensified by reduction of medium use and automated process control. • The process achieved cell density over 40 × 10(6) cells/mL and virus yield over 4.37 log(10)(HAU/100 μL). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-020-11050-8. |
format | Online Article Text |
id | pubmed-7847233 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-78472332021-02-01 High cell density perfusion process for high yield of influenza A virus production using MDCK suspension cells Wu, Yixiao Bissinger, Thomas Genzel, Yvonne Liu, Xuping Reichl, Udo Tan, Wen-Song Appl Microbiol Biotechnol Biotechnological Products and Process Engineering ABSTRACT: Similar to the recent COVID-19 pandemic, influenza A virus poses a constant threat to the global community. For the treatment of flu disease, both antivirals and vaccines are available with vaccines the most effective and safest approach. In order to overcome limitations in egg-based vaccine manufacturing, cell culture–based processes have been established. While this production method avoids egg-associated risks in face of pandemics, process intensification using animal suspension cells in high cell density perfusion cultures should allow to further increase manufacturing capacities worldwide. In this work, we demonstrate the development of a perfusion process using Madin-Darby canine kidney (MDCK) suspension cells for influenza A (H1N1) virus production from scale-down shake flask cultivations to laboratory scale stirred tank bioreactors. Shake flask cultivations using semi-perfusion mode enabled high-yield virus harvests (4.25 log(10)(HAU/100 μL)) from MDCK cells grown up to 41 × 10(6) cells/mL. Scale-up to bioreactors with an alternating tangential flow (ATF) perfusion system required optimization of pH control and implementation of a temperature shift during the infection phase. Use of a capacitance probe for on-line perfusion control allowed to minimize medium consumption. This contributed to a better process control and a more economical performance while maintaining a maximum virus titer of 4.37 log(10)(HAU/100 μL) and an infectious virus titer of 1.83 × 10(10) virions/mL. Overall, this study clearly demonstrates recent advances in cell culture–based perfusion processes for next-generation high-yield influenza vaccine manufacturing for pandemic preparedness. KEY POINTS: • First MDCK suspension cell–based perfusion process for IAV produciton was established. • “Cell density effect” was overcome and process was intensified by reduction of medium use and automated process control. • The process achieved cell density over 40 × 10(6) cells/mL and virus yield over 4.37 log(10)(HAU/100 μL). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-020-11050-8. Springer Berlin Heidelberg 2021-01-30 2021 /pmc/articles/PMC7847233/ /pubmed/33515287 http://dx.doi.org/10.1007/s00253-020-11050-8 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Biotechnological Products and Process Engineering Wu, Yixiao Bissinger, Thomas Genzel, Yvonne Liu, Xuping Reichl, Udo Tan, Wen-Song High cell density perfusion process for high yield of influenza A virus production using MDCK suspension cells |
title | High cell density perfusion process for high yield of influenza A virus production using MDCK suspension cells |
title_full | High cell density perfusion process for high yield of influenza A virus production using MDCK suspension cells |
title_fullStr | High cell density perfusion process for high yield of influenza A virus production using MDCK suspension cells |
title_full_unstemmed | High cell density perfusion process for high yield of influenza A virus production using MDCK suspension cells |
title_short | High cell density perfusion process for high yield of influenza A virus production using MDCK suspension cells |
title_sort | high cell density perfusion process for high yield of influenza a virus production using mdck suspension cells |
topic | Biotechnological Products and Process Engineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7847233/ https://www.ncbi.nlm.nih.gov/pubmed/33515287 http://dx.doi.org/10.1007/s00253-020-11050-8 |
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