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Development and Evaluation of Vero Cell-Derived Master Donor Viruses for Influenza Pandemic Preparedness
The embryonated egg-based platform currently produces the majority of seasonal influenza vaccines by employing a well-developed master donor virus (MDV, A/PR/8/34 (PR8)) to generate high-growth reassortants (HGRs) for A/H1N1 and A/H3N2 subtypes. Although the egg-based platform can supply enough seas...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7712210/ https://www.ncbi.nlm.nih.gov/pubmed/33113866 http://dx.doi.org/10.3390/vaccines8040626 |
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author | Chen, Po-Ling Tzeng, Tsai-Teng Hu, Alan Yung-Chih Wang, Lily Hui-Ching Lee, Min-Shi |
author_facet | Chen, Po-Ling Tzeng, Tsai-Teng Hu, Alan Yung-Chih Wang, Lily Hui-Ching Lee, Min-Shi |
author_sort | Chen, Po-Ling |
collection | PubMed |
description | The embryonated egg-based platform currently produces the majority of seasonal influenza vaccines by employing a well-developed master donor virus (MDV, A/PR/8/34 (PR8)) to generate high-growth reassortants (HGRs) for A/H1N1 and A/H3N2 subtypes. Although the egg-based platform can supply enough seasonal influenza vaccines, it cannot meet surging demands during influenza pandemics. Therefore, multi-purpose platforms are desirable for pandemic preparedness. The Vero cell-based production platform is widely used for human vaccines and could be a potential multi-purpose platform for pandemic influenza vaccines. However, many wild-type and egg-derived influenza viruses cannot grow efficiently in Vero cells. Therefore, it is critical to develop Vero cell-derived high-growth MDVs for pandemic preparedness. In this study, we evaluated two in-house MDVs (Vero-15 and VB5) and two external MDVs (PR8 and PR8-HY) to generate Vero cell-derived HGRs for five avian influenza viruses (AIVs) with pandemic potentials (H5N1 clade 2.3.4, H5N1 clade 2.3.2.1, American-lineage H5N2, H7N9 first wave and H7N9 fifth wave). Overall, no single MDV could generate HGRs for all five AIVs, but this goal could be achieved by employing two in-house MDVs (vB5 and Vero-15). In immunization studies, mice received two doses of Vero cell-derived inactivated H5N1 and H7N9 whole virus antigens adjuvanted with alum and developed robust antibody responses. |
format | Online Article Text |
id | pubmed-7712210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77122102020-12-04 Development and Evaluation of Vero Cell-Derived Master Donor Viruses for Influenza Pandemic Preparedness Chen, Po-Ling Tzeng, Tsai-Teng Hu, Alan Yung-Chih Wang, Lily Hui-Ching Lee, Min-Shi Vaccines (Basel) Article The embryonated egg-based platform currently produces the majority of seasonal influenza vaccines by employing a well-developed master donor virus (MDV, A/PR/8/34 (PR8)) to generate high-growth reassortants (HGRs) for A/H1N1 and A/H3N2 subtypes. Although the egg-based platform can supply enough seasonal influenza vaccines, it cannot meet surging demands during influenza pandemics. Therefore, multi-purpose platforms are desirable for pandemic preparedness. The Vero cell-based production platform is widely used for human vaccines and could be a potential multi-purpose platform for pandemic influenza vaccines. However, many wild-type and egg-derived influenza viruses cannot grow efficiently in Vero cells. Therefore, it is critical to develop Vero cell-derived high-growth MDVs for pandemic preparedness. In this study, we evaluated two in-house MDVs (Vero-15 and VB5) and two external MDVs (PR8 and PR8-HY) to generate Vero cell-derived HGRs for five avian influenza viruses (AIVs) with pandemic potentials (H5N1 clade 2.3.4, H5N1 clade 2.3.2.1, American-lineage H5N2, H7N9 first wave and H7N9 fifth wave). Overall, no single MDV could generate HGRs for all five AIVs, but this goal could be achieved by employing two in-house MDVs (vB5 and Vero-15). In immunization studies, mice received two doses of Vero cell-derived inactivated H5N1 and H7N9 whole virus antigens adjuvanted with alum and developed robust antibody responses. MDPI 2020-10-25 /pmc/articles/PMC7712210/ /pubmed/33113866 http://dx.doi.org/10.3390/vaccines8040626 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Chen, Po-Ling Tzeng, Tsai-Teng Hu, Alan Yung-Chih Wang, Lily Hui-Ching Lee, Min-Shi Development and Evaluation of Vero Cell-Derived Master Donor Viruses for Influenza Pandemic Preparedness |
title | Development and Evaluation of Vero Cell-Derived Master Donor Viruses for Influenza Pandemic Preparedness |
title_full | Development and Evaluation of Vero Cell-Derived Master Donor Viruses for Influenza Pandemic Preparedness |
title_fullStr | Development and Evaluation of Vero Cell-Derived Master Donor Viruses for Influenza Pandemic Preparedness |
title_full_unstemmed | Development and Evaluation of Vero Cell-Derived Master Donor Viruses for Influenza Pandemic Preparedness |
title_short | Development and Evaluation of Vero Cell-Derived Master Donor Viruses for Influenza Pandemic Preparedness |
title_sort | development and evaluation of vero cell-derived master donor viruses for influenza pandemic preparedness |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7712210/ https://www.ncbi.nlm.nih.gov/pubmed/33113866 http://dx.doi.org/10.3390/vaccines8040626 |
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