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Influenza B vaccine lineage selection—An optimized trivalent vaccine

Epidemics of seasonal influenza viruses cause considerable morbidity and mortality each year. Various types and subtypes of influenza circulate in humans and evolve continuously such that individuals at risk of serious complications need to be vaccinated annually to keep protection up to date with c...

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Detalles Bibliográficos
Autores principales: Mosterín Höpping, Ana, Fonville, Judith M., Russell, Colin A., James, Sarah, Smith, Derek J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793086/
https://www.ncbi.nlm.nih.gov/pubmed/26896685
http://dx.doi.org/10.1016/j.vaccine.2016.01.042
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author Mosterín Höpping, Ana
Fonville, Judith M.
Russell, Colin A.
James, Sarah
Smith, Derek J.
author_facet Mosterín Höpping, Ana
Fonville, Judith M.
Russell, Colin A.
James, Sarah
Smith, Derek J.
author_sort Mosterín Höpping, Ana
collection PubMed
description Epidemics of seasonal influenza viruses cause considerable morbidity and mortality each year. Various types and subtypes of influenza circulate in humans and evolve continuously such that individuals at risk of serious complications need to be vaccinated annually to keep protection up to date with circulating viruses. The influenza vaccine in most parts of the world is a trivalent vaccine, including an antigenically representative virus of recently circulating influenza A/H3N2, A/H1N1, and influenza B viruses. However, since the 1970s influenza B has split into two antigenically distinct lineages, only one of which is represented in the annual trivalent vaccine at any time. We describe a lineage selection strategy that optimizes protection against influenza B using the standard trivalent vaccine as a potentially cost effective alternative to quadrivalent vaccines.
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spelling pubmed-47930862016-03-24 Influenza B vaccine lineage selection—An optimized trivalent vaccine Mosterín Höpping, Ana Fonville, Judith M. Russell, Colin A. James, Sarah Smith, Derek J. Vaccine Article Epidemics of seasonal influenza viruses cause considerable morbidity and mortality each year. Various types and subtypes of influenza circulate in humans and evolve continuously such that individuals at risk of serious complications need to be vaccinated annually to keep protection up to date with circulating viruses. The influenza vaccine in most parts of the world is a trivalent vaccine, including an antigenically representative virus of recently circulating influenza A/H3N2, A/H1N1, and influenza B viruses. However, since the 1970s influenza B has split into two antigenically distinct lineages, only one of which is represented in the annual trivalent vaccine at any time. We describe a lineage selection strategy that optimizes protection against influenza B using the standard trivalent vaccine as a potentially cost effective alternative to quadrivalent vaccines. Elsevier Science 2016-03-18 /pmc/articles/PMC4793086/ /pubmed/26896685 http://dx.doi.org/10.1016/j.vaccine.2016.01.042 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Mosterín Höpping, Ana
Fonville, Judith M.
Russell, Colin A.
James, Sarah
Smith, Derek J.
Influenza B vaccine lineage selection—An optimized trivalent vaccine
title Influenza B vaccine lineage selection—An optimized trivalent vaccine
title_full Influenza B vaccine lineage selection—An optimized trivalent vaccine
title_fullStr Influenza B vaccine lineage selection—An optimized trivalent vaccine
title_full_unstemmed Influenza B vaccine lineage selection—An optimized trivalent vaccine
title_short Influenza B vaccine lineage selection—An optimized trivalent vaccine
title_sort influenza b vaccine lineage selection—an optimized trivalent vaccine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793086/
https://www.ncbi.nlm.nih.gov/pubmed/26896685
http://dx.doi.org/10.1016/j.vaccine.2016.01.042
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