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Prospects for Universal Influenza Virus Vaccine

The current vaccination strategy against influenza A and B viruses is vulnerable to the unanticipated emergence of epidemic strains that are poorly matched by the vaccine. A vaccine that is less sensitive to the antigenic evolution of the virus would be a major improvement. The general feasibility o...

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Autores principales: Gerhard, Walter, Mozdzanowska, Krystyna, Zharikova, Darya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Centers for Disease Control and Prevention 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3294695/
https://www.ncbi.nlm.nih.gov/pubmed/16704803
http://dx.doi.org/10.3201/eid1204.051020
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author Gerhard, Walter
Mozdzanowska, Krystyna
Zharikova, Darya
author_facet Gerhard, Walter
Mozdzanowska, Krystyna
Zharikova, Darya
author_sort Gerhard, Walter
collection PubMed
description The current vaccination strategy against influenza A and B viruses is vulnerable to the unanticipated emergence of epidemic strains that are poorly matched by the vaccine. A vaccine that is less sensitive to the antigenic evolution of the virus would be a major improvement. The general feasibility of this goal is supported by studies in animal models that show that immunologic activities directed against relatively invariant viral determinants can reduce illness and death. The most promising approaches are based on antibodies specific for the relatively conserved ectodomain of matrix protein 2 and the intersubunit region of hemagglutinin. However, additional conserved determinants for protective antibodies are likely to exist, and their identification should be encouraged. Most importantly, infection and current vaccines do not appear to effectively induce these antibodies in humans. This finding provides a powerful rationale for testing the protective activity of these relatively conserved viral components in humans.
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spelling pubmed-32946952012-03-06 Prospects for Universal Influenza Virus Vaccine Gerhard, Walter Mozdzanowska, Krystyna Zharikova, Darya Emerg Infect Dis Perspective The current vaccination strategy against influenza A and B viruses is vulnerable to the unanticipated emergence of epidemic strains that are poorly matched by the vaccine. A vaccine that is less sensitive to the antigenic evolution of the virus would be a major improvement. The general feasibility of this goal is supported by studies in animal models that show that immunologic activities directed against relatively invariant viral determinants can reduce illness and death. The most promising approaches are based on antibodies specific for the relatively conserved ectodomain of matrix protein 2 and the intersubunit region of hemagglutinin. However, additional conserved determinants for protective antibodies are likely to exist, and their identification should be encouraged. Most importantly, infection and current vaccines do not appear to effectively induce these antibodies in humans. This finding provides a powerful rationale for testing the protective activity of these relatively conserved viral components in humans. Centers for Disease Control and Prevention 2006-04 /pmc/articles/PMC3294695/ /pubmed/16704803 http://dx.doi.org/10.3201/eid1204.051020 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited.
spellingShingle Perspective
Gerhard, Walter
Mozdzanowska, Krystyna
Zharikova, Darya
Prospects for Universal Influenza Virus Vaccine
title Prospects for Universal Influenza Virus Vaccine
title_full Prospects for Universal Influenza Virus Vaccine
title_fullStr Prospects for Universal Influenza Virus Vaccine
title_full_unstemmed Prospects for Universal Influenza Virus Vaccine
title_short Prospects for Universal Influenza Virus Vaccine
title_sort prospects for universal influenza virus vaccine
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3294695/
https://www.ncbi.nlm.nih.gov/pubmed/16704803
http://dx.doi.org/10.3201/eid1204.051020
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