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Evaluation of MDCK Cell-Derived Influenza H7N9 Vaccine Candidates in Ferrets
Avian-origin influenza A (H7N9) viruses emerged as human pathogens in China in early 2013 and have killed >100 persons. Influenza vaccines are mainly manufactured using egg-based technology which could not meet the surging demand during influenza pandemics. In this study, we evaluated cell-based...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4370571/ https://www.ncbi.nlm.nih.gov/pubmed/25799397 http://dx.doi.org/10.1371/journal.pone.0120793 |
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author | Chia, Min-Yuan Hu, Alan Yung-Chih Tseng, Yu-Fen Weng, Tsai-Chuan Lai, Chia-Chun Lin, Jun-Yang Chen, Po-Ling Wang, Ya-Fang Chao, Sin-Ru Chang, Jui-Yuan Hwang, Yi-Shiuh Yeh, Chia-Tsui Yu, Cheng-Ping Chen, Yee-Chun Su, Ih-Jen Lee, Min-Shi |
author_facet | Chia, Min-Yuan Hu, Alan Yung-Chih Tseng, Yu-Fen Weng, Tsai-Chuan Lai, Chia-Chun Lin, Jun-Yang Chen, Po-Ling Wang, Ya-Fang Chao, Sin-Ru Chang, Jui-Yuan Hwang, Yi-Shiuh Yeh, Chia-Tsui Yu, Cheng-Ping Chen, Yee-Chun Su, Ih-Jen Lee, Min-Shi |
author_sort | Chia, Min-Yuan |
collection | PubMed |
description | Avian-origin influenza A (H7N9) viruses emerged as human pathogens in China in early 2013 and have killed >100 persons. Influenza vaccines are mainly manufactured using egg-based technology which could not meet the surging demand during influenza pandemics. In this study, we evaluated cell-based influenza H7N9 vaccines in ferrets. An egg-derived influenza H7N9 reassortant vaccine virus was adapted in MDCK cells. Influenza H7N9 whole virus vaccine antigen was manufactured using a microcarrier-based culture system. Immunogenicity and protection of the vaccine candidates with three different formulations (300μg aluminum hydroxide, 1.5μg HA, and 1.5μg HA plus 300μg aluminum hydroxide) were evaluated in ferrets. In ferrets receiving two doses of vaccination, geometric mean titers of hemagglutination (HA) inhibition and neutralizing antibodies were <10 and <40 for the control group (adjuvant only), 17 and 80 for the unadjuvanted (HA only) group, and 190 and 640 for the adjuvanted group (HA plus adjuvant), respectively. After challenge with wild-type influenza H7N9 viruses, virus titers in respiratory tracts of the adjuvanted group were significantly lower than that in the control, and unadjuvanted groups. MDCK cell-derived influenza H7N9 whole virus vaccine candidate is immunogenic and protective in ferrets and clinical development is highly warranted. |
format | Online Article Text |
id | pubmed-4370571 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-43705712015-04-04 Evaluation of MDCK Cell-Derived Influenza H7N9 Vaccine Candidates in Ferrets Chia, Min-Yuan Hu, Alan Yung-Chih Tseng, Yu-Fen Weng, Tsai-Chuan Lai, Chia-Chun Lin, Jun-Yang Chen, Po-Ling Wang, Ya-Fang Chao, Sin-Ru Chang, Jui-Yuan Hwang, Yi-Shiuh Yeh, Chia-Tsui Yu, Cheng-Ping Chen, Yee-Chun Su, Ih-Jen Lee, Min-Shi PLoS One Research Article Avian-origin influenza A (H7N9) viruses emerged as human pathogens in China in early 2013 and have killed >100 persons. Influenza vaccines are mainly manufactured using egg-based technology which could not meet the surging demand during influenza pandemics. In this study, we evaluated cell-based influenza H7N9 vaccines in ferrets. An egg-derived influenza H7N9 reassortant vaccine virus was adapted in MDCK cells. Influenza H7N9 whole virus vaccine antigen was manufactured using a microcarrier-based culture system. Immunogenicity and protection of the vaccine candidates with three different formulations (300μg aluminum hydroxide, 1.5μg HA, and 1.5μg HA plus 300μg aluminum hydroxide) were evaluated in ferrets. In ferrets receiving two doses of vaccination, geometric mean titers of hemagglutination (HA) inhibition and neutralizing antibodies were <10 and <40 for the control group (adjuvant only), 17 and 80 for the unadjuvanted (HA only) group, and 190 and 640 for the adjuvanted group (HA plus adjuvant), respectively. After challenge with wild-type influenza H7N9 viruses, virus titers in respiratory tracts of the adjuvanted group were significantly lower than that in the control, and unadjuvanted groups. MDCK cell-derived influenza H7N9 whole virus vaccine candidate is immunogenic and protective in ferrets and clinical development is highly warranted. Public Library of Science 2015-03-23 /pmc/articles/PMC4370571/ /pubmed/25799397 http://dx.doi.org/10.1371/journal.pone.0120793 Text en © 2015 Chia et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Chia, Min-Yuan Hu, Alan Yung-Chih Tseng, Yu-Fen Weng, Tsai-Chuan Lai, Chia-Chun Lin, Jun-Yang Chen, Po-Ling Wang, Ya-Fang Chao, Sin-Ru Chang, Jui-Yuan Hwang, Yi-Shiuh Yeh, Chia-Tsui Yu, Cheng-Ping Chen, Yee-Chun Su, Ih-Jen Lee, Min-Shi Evaluation of MDCK Cell-Derived Influenza H7N9 Vaccine Candidates in Ferrets |
title | Evaluation of MDCK Cell-Derived Influenza H7N9 Vaccine Candidates in Ferrets |
title_full | Evaluation of MDCK Cell-Derived Influenza H7N9 Vaccine Candidates in Ferrets |
title_fullStr | Evaluation of MDCK Cell-Derived Influenza H7N9 Vaccine Candidates in Ferrets |
title_full_unstemmed | Evaluation of MDCK Cell-Derived Influenza H7N9 Vaccine Candidates in Ferrets |
title_short | Evaluation of MDCK Cell-Derived Influenza H7N9 Vaccine Candidates in Ferrets |
title_sort | evaluation of mdck cell-derived influenza h7n9 vaccine candidates in ferrets |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4370571/ https://www.ncbi.nlm.nih.gov/pubmed/25799397 http://dx.doi.org/10.1371/journal.pone.0120793 |
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