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Neutralization antibody response to booster/priming immunization with new equine influenza vaccine in Japan
Equine influenza (EI) vaccine has been widely used. However, the causative EI virus (H3N8) undergoes continuous antigenic drift, and the vaccine strains must be periodically reviewed and if necessary, updated to maintain vaccine efficacy against circulating viruses. In 2016, the Japanese vaccine was...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Japanese Society of Veterinary Science
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836781/ https://www.ncbi.nlm.nih.gov/pubmed/29237998 http://dx.doi.org/10.1292/jvms.17-0538 |
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author | YAMANAKA, Takashi NEMOTO, Manabu BANNAI, Hiroshi TSUJIMURA, Koji MATSUMURA, Tomio KOKADO, Hiroshi GILDEA, Sarah CULLINANE, Ann |
author_facet | YAMANAKA, Takashi NEMOTO, Manabu BANNAI, Hiroshi TSUJIMURA, Koji MATSUMURA, Tomio KOKADO, Hiroshi GILDEA, Sarah CULLINANE, Ann |
author_sort | YAMANAKA, Takashi |
collection | PubMed |
description | Equine influenza (EI) vaccine has been widely used. However, the causative EI virus (H3N8) undergoes continuous antigenic drift, and the vaccine strains must be periodically reviewed and if necessary, updated to maintain vaccine efficacy against circulating viruses. In 2016, the Japanese vaccine was updated by replacing the old viruses with the Florida sub-lineage Clade (Fc) 2 virus, A/equine/Yokohama/aq13/2010 (Y10). We investigated the virus neutralization (VN) antibody response to Fc2 viruses currently circulating in Europe, after booster or primary immunization with the new vaccine. These European viruses have the amino acid substitution A144V or I179V of the hemagglutinin. In horses that had previously received a primary course and bi-annual boosters with the old vaccine booster, immunization with the updated vaccine increased the VN antibody levels against the European Fc2 viruses as well as Y10. There were no significant differences in the VN titers against Y10 and the Fc2 viruses with A144V or I179V substitution in horses that had received a primary course of the updated vaccine. However, a mixed primary course where the first dose was the old vaccine and the second dose was the updated vaccine, reduced VN titers against the European viruses compared to that against Y10. In summary, the new vaccine affords horses protective level of VN titers against the Fc2 viruses carrying A144V or I179V substitution, but our results suggest that the combination of the old and new vaccines for primary immunization would not be optimum. |
format | Online Article Text |
id | pubmed-5836781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Japanese Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-58367812018-03-09 Neutralization antibody response to booster/priming immunization with new equine influenza vaccine in Japan YAMANAKA, Takashi NEMOTO, Manabu BANNAI, Hiroshi TSUJIMURA, Koji MATSUMURA, Tomio KOKADO, Hiroshi GILDEA, Sarah CULLINANE, Ann J Vet Med Sci Virology Equine influenza (EI) vaccine has been widely used. However, the causative EI virus (H3N8) undergoes continuous antigenic drift, and the vaccine strains must be periodically reviewed and if necessary, updated to maintain vaccine efficacy against circulating viruses. In 2016, the Japanese vaccine was updated by replacing the old viruses with the Florida sub-lineage Clade (Fc) 2 virus, A/equine/Yokohama/aq13/2010 (Y10). We investigated the virus neutralization (VN) antibody response to Fc2 viruses currently circulating in Europe, after booster or primary immunization with the new vaccine. These European viruses have the amino acid substitution A144V or I179V of the hemagglutinin. In horses that had previously received a primary course and bi-annual boosters with the old vaccine booster, immunization with the updated vaccine increased the VN antibody levels against the European Fc2 viruses as well as Y10. There were no significant differences in the VN titers against Y10 and the Fc2 viruses with A144V or I179V substitution in horses that had received a primary course of the updated vaccine. However, a mixed primary course where the first dose was the old vaccine and the second dose was the updated vaccine, reduced VN titers against the European viruses compared to that against Y10. In summary, the new vaccine affords horses protective level of VN titers against the Fc2 viruses carrying A144V or I179V substitution, but our results suggest that the combination of the old and new vaccines for primary immunization would not be optimum. The Japanese Society of Veterinary Science 2017-12-14 2018-02 /pmc/articles/PMC5836781/ /pubmed/29237998 http://dx.doi.org/10.1292/jvms.17-0538 Text en ©2018 The Japanese Society of Veterinary Science This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Virology YAMANAKA, Takashi NEMOTO, Manabu BANNAI, Hiroshi TSUJIMURA, Koji MATSUMURA, Tomio KOKADO, Hiroshi GILDEA, Sarah CULLINANE, Ann Neutralization antibody response to booster/priming immunization with new equine influenza vaccine in Japan |
title | Neutralization antibody response to booster/priming immunization with new
equine influenza vaccine in Japan |
title_full | Neutralization antibody response to booster/priming immunization with new
equine influenza vaccine in Japan |
title_fullStr | Neutralization antibody response to booster/priming immunization with new
equine influenza vaccine in Japan |
title_full_unstemmed | Neutralization antibody response to booster/priming immunization with new
equine influenza vaccine in Japan |
title_short | Neutralization antibody response to booster/priming immunization with new
equine influenza vaccine in Japan |
title_sort | neutralization antibody response to booster/priming immunization with new
equine influenza vaccine in japan |
topic | Virology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836781/ https://www.ncbi.nlm.nih.gov/pubmed/29237998 http://dx.doi.org/10.1292/jvms.17-0538 |
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