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Membrane Chromatography-Based Downstream Processing for Cell-Culture Produced Influenza Vaccines

New influenza strains are constantly emerging, causing seasonal epidemics and raising concerns to the risk of a new global pandemic. Since vaccination is an effective method to prevent the spread of the disease and reduce its severity, the development of robust bioprocesses for producing pandemic in...

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Autores principales: Yang, Zeyu, Xu, Xingge, Silva, Cristina A. T., Farnos, Omar, Venereo-Sanchez, Alina, Toussaint, Cécile, Dash, Shantoshini, González-Domínguez, Irene, Bernier, Alice, Henry, Olivier, Kamen, Amine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9414887/
https://www.ncbi.nlm.nih.gov/pubmed/36016198
http://dx.doi.org/10.3390/vaccines10081310
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author Yang, Zeyu
Xu, Xingge
Silva, Cristina A. T.
Farnos, Omar
Venereo-Sanchez, Alina
Toussaint, Cécile
Dash, Shantoshini
González-Domínguez, Irene
Bernier, Alice
Henry, Olivier
Kamen, Amine
author_facet Yang, Zeyu
Xu, Xingge
Silva, Cristina A. T.
Farnos, Omar
Venereo-Sanchez, Alina
Toussaint, Cécile
Dash, Shantoshini
González-Domínguez, Irene
Bernier, Alice
Henry, Olivier
Kamen, Amine
author_sort Yang, Zeyu
collection PubMed
description New influenza strains are constantly emerging, causing seasonal epidemics and raising concerns to the risk of a new global pandemic. Since vaccination is an effective method to prevent the spread of the disease and reduce its severity, the development of robust bioprocesses for producing pandemic influenza vaccines is exceptionally important. Herein, a membrane chromatography-based downstream processing platform with a demonstrated industrial application potential was established. Cell culture-derived influenza virus H1N1/A/PR/8/34 was harvested from benchtop bioreactor cultures. For the clarification of the cell culture broth, a depth filtration was selected as an alternative to centrifugation. After inactivation, an anion exchange chromatography membrane was used for viral capture and further processing. Additionally, two pandemic influenza virus strains, the H7N9 subtype of the A/Anhui/1/2013 and H3N2/A/Hong Kong/8/64, were successfully processed through similar downstream process steps establishing optimized process parameters. Overall, 41.3–62.5% viral recovery was achieved, with the removal of 86.3–96.5% host cell DNA and 95.5–99.7% of proteins. The proposed membrane chromatography purification is a scalable and generic method for the processing of different influenza strains and is a promising alternative to the current industrial purification of influenza vaccines based on ultracentrifugation methodologies.
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spelling pubmed-94148872022-08-27 Membrane Chromatography-Based Downstream Processing for Cell-Culture Produced Influenza Vaccines Yang, Zeyu Xu, Xingge Silva, Cristina A. T. Farnos, Omar Venereo-Sanchez, Alina Toussaint, Cécile Dash, Shantoshini González-Domínguez, Irene Bernier, Alice Henry, Olivier Kamen, Amine Vaccines (Basel) Article New influenza strains are constantly emerging, causing seasonal epidemics and raising concerns to the risk of a new global pandemic. Since vaccination is an effective method to prevent the spread of the disease and reduce its severity, the development of robust bioprocesses for producing pandemic influenza vaccines is exceptionally important. Herein, a membrane chromatography-based downstream processing platform with a demonstrated industrial application potential was established. Cell culture-derived influenza virus H1N1/A/PR/8/34 was harvested from benchtop bioreactor cultures. For the clarification of the cell culture broth, a depth filtration was selected as an alternative to centrifugation. After inactivation, an anion exchange chromatography membrane was used for viral capture and further processing. Additionally, two pandemic influenza virus strains, the H7N9 subtype of the A/Anhui/1/2013 and H3N2/A/Hong Kong/8/64, were successfully processed through similar downstream process steps establishing optimized process parameters. Overall, 41.3–62.5% viral recovery was achieved, with the removal of 86.3–96.5% host cell DNA and 95.5–99.7% of proteins. The proposed membrane chromatography purification is a scalable and generic method for the processing of different influenza strains and is a promising alternative to the current industrial purification of influenza vaccines based on ultracentrifugation methodologies. MDPI 2022-08-13 /pmc/articles/PMC9414887/ /pubmed/36016198 http://dx.doi.org/10.3390/vaccines10081310 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yang, Zeyu
Xu, Xingge
Silva, Cristina A. T.
Farnos, Omar
Venereo-Sanchez, Alina
Toussaint, Cécile
Dash, Shantoshini
González-Domínguez, Irene
Bernier, Alice
Henry, Olivier
Kamen, Amine
Membrane Chromatography-Based Downstream Processing for Cell-Culture Produced Influenza Vaccines
title Membrane Chromatography-Based Downstream Processing for Cell-Culture Produced Influenza Vaccines
title_full Membrane Chromatography-Based Downstream Processing for Cell-Culture Produced Influenza Vaccines
title_fullStr Membrane Chromatography-Based Downstream Processing for Cell-Culture Produced Influenza Vaccines
title_full_unstemmed Membrane Chromatography-Based Downstream Processing for Cell-Culture Produced Influenza Vaccines
title_short Membrane Chromatography-Based Downstream Processing for Cell-Culture Produced Influenza Vaccines
title_sort membrane chromatography-based downstream processing for cell-culture produced influenza vaccines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9414887/
https://www.ncbi.nlm.nih.gov/pubmed/36016198
http://dx.doi.org/10.3390/vaccines10081310
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