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Induction of a Protective Heterosubtypic Immune Response Against the Influenza Virus by using Recombinant Adenoviral Vectors Expressing Hemagglutinin of the Influenza H5 Virus
Abstract Influenza viruses are characterized by a high degree of antigenic variability, which causes the annual emergence of flu epidemics and irregularly timed pandemics caused by viruses with new antigenic and biological traits. Novel approaches to vaccination can help circumvent this problem. One...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
A.I. Gordeyev
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3347542/ https://www.ncbi.nlm.nih.gov/pubmed/22649637 |
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author | Shmarov, M.M. Sedova, E.S. Verkhovskaya, L.V. Rudneva, I.A. Bogacheva, E.A. Barykova, Yu.A. Shcherbinin, D.N. Lysenko, A.A. Tutykhina, I.L. Logunov, D.Y. Smirnov, Yu.A. Naroditsky, B.S. Gintsburg, A.L. |
author_facet | Shmarov, M.M. Sedova, E.S. Verkhovskaya, L.V. Rudneva, I.A. Bogacheva, E.A. Barykova, Yu.A. Shcherbinin, D.N. Lysenko, A.A. Tutykhina, I.L. Logunov, D.Y. Smirnov, Yu.A. Naroditsky, B.S. Gintsburg, A.L. |
author_sort | Shmarov, M.M. |
collection | PubMed |
description | Abstract Influenza viruses are characterized by a high degree of antigenic variability, which causes the annual emergence of flu epidemics and irregularly timed pandemics caused by viruses with new antigenic and biological traits. Novel approaches to vaccination can help circumvent this problem. One of these new methods incorporates genetic vaccines based on adenoviral vectors. Recombinant adenoviral vectors which contain hemagglutinin–encoding genes from avian H5N1 and H5N2 (Ad–HA5–1 and Ad–HA5–2) influenza viruses were obtained using the AdEasy Adenoviral Vector System (Stratagene). Laboratory mice received a double intranasal vaccination with Ad–HA5–1 and Ad–HA5–2. This study demonstrates that immunization with recombinant adenoviruses bearing the Н 5 influenza virus hemagglutinin gene induces a immune response which protects immunized mice from a lethal dose of the H5 influenza virus. Moreover, it also protects the host from a lethal dose of the H1 virus, which belongs to the same clade as H5, but does not confer protection from the subtype H3 influenza virus, which belongs to a different clade. |
format | Online Article Text |
id | pubmed-3347542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | A.I. Gordeyev |
record_format | MEDLINE/PubMed |
spelling | pubmed-33475422012-05-30 Induction of a Protective Heterosubtypic Immune Response Against the Influenza Virus by using Recombinant Adenoviral Vectors Expressing Hemagglutinin of the Influenza H5 Virus Shmarov, M.M. Sedova, E.S. Verkhovskaya, L.V. Rudneva, I.A. Bogacheva, E.A. Barykova, Yu.A. Shcherbinin, D.N. Lysenko, A.A. Tutykhina, I.L. Logunov, D.Y. Smirnov, Yu.A. Naroditsky, B.S. Gintsburg, A.L. Acta Naturae Research Article Abstract Influenza viruses are characterized by a high degree of antigenic variability, which causes the annual emergence of flu epidemics and irregularly timed pandemics caused by viruses with new antigenic and biological traits. Novel approaches to vaccination can help circumvent this problem. One of these new methods incorporates genetic vaccines based on adenoviral vectors. Recombinant adenoviral vectors which contain hemagglutinin–encoding genes from avian H5N1 and H5N2 (Ad–HA5–1 and Ad–HA5–2) influenza viruses were obtained using the AdEasy Adenoviral Vector System (Stratagene). Laboratory mice received a double intranasal vaccination with Ad–HA5–1 and Ad–HA5–2. This study demonstrates that immunization with recombinant adenoviruses bearing the Н 5 influenza virus hemagglutinin gene induces a immune response which protects immunized mice from a lethal dose of the H5 influenza virus. Moreover, it also protects the host from a lethal dose of the H1 virus, which belongs to the same clade as H5, but does not confer protection from the subtype H3 influenza virus, which belongs to a different clade. A.I. Gordeyev 2010-04 /pmc/articles/PMC3347542/ /pubmed/22649637 Text en Copyright © 2010 Park-media Ltd. http://creativecommons.org/licenses/by/2.0/ 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 work is properly cited. |
spellingShingle | Research Article Shmarov, M.M. Sedova, E.S. Verkhovskaya, L.V. Rudneva, I.A. Bogacheva, E.A. Barykova, Yu.A. Shcherbinin, D.N. Lysenko, A.A. Tutykhina, I.L. Logunov, D.Y. Smirnov, Yu.A. Naroditsky, B.S. Gintsburg, A.L. Induction of a Protective Heterosubtypic Immune Response Against the Influenza Virus by using Recombinant Adenoviral Vectors Expressing Hemagglutinin of the Influenza H5 Virus |
title | Induction of a Protective Heterosubtypic Immune Response Against the Influenza Virus by using Recombinant Adenoviral Vectors Expressing Hemagglutinin of the Influenza H5 Virus |
title_full | Induction of a Protective Heterosubtypic Immune Response Against the Influenza Virus by using Recombinant Adenoviral Vectors Expressing Hemagglutinin of the Influenza H5 Virus |
title_fullStr | Induction of a Protective Heterosubtypic Immune Response Against the Influenza Virus by using Recombinant Adenoviral Vectors Expressing Hemagglutinin of the Influenza H5 Virus |
title_full_unstemmed | Induction of a Protective Heterosubtypic Immune Response Against the Influenza Virus by using Recombinant Adenoviral Vectors Expressing Hemagglutinin of the Influenza H5 Virus |
title_short | Induction of a Protective Heterosubtypic Immune Response Against the Influenza Virus by using Recombinant Adenoviral Vectors Expressing Hemagglutinin of the Influenza H5 Virus |
title_sort | induction of a protective heterosubtypic immune response against the influenza virus by using recombinant adenoviral vectors expressing hemagglutinin of the influenza h5 virus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3347542/ https://www.ncbi.nlm.nih.gov/pubmed/22649637 |
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