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Matrix Protein 2 Vaccination and Protection against Influenza Viruses, Including Subtype H5N1
Changes in influenza viruses require regular reformulation of strain-specific influenza vaccines. Vaccines based on conserved antigens provide broader protection. Influenza matrix protein 2 (M2) is highly conserved across influenza A subtypes. To evaluate its efficacy as a vaccine candidate, we vacc...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Centers for Disease Control and Prevention
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2725899/ https://www.ncbi.nlm.nih.gov/pubmed/17552096 http://dx.doi.org/10.3201/eid1303.061125 |
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author | Tompkins, Stephen Mark Zhao, Zi-Shan Lo, Chia-Yun Misplon, Julia A. Liu, Teresa Ye, Zhiping Hogan, Robert J. Wu, Zhengqi Benton, Kimberly A. Tumpey, Terrence M. Epstein, Suzanne L. |
author_facet | Tompkins, Stephen Mark Zhao, Zi-Shan Lo, Chia-Yun Misplon, Julia A. Liu, Teresa Ye, Zhiping Hogan, Robert J. Wu, Zhengqi Benton, Kimberly A. Tumpey, Terrence M. Epstein, Suzanne L. |
author_sort | Tompkins, Stephen Mark |
collection | PubMed |
description | Changes in influenza viruses require regular reformulation of strain-specific influenza vaccines. Vaccines based on conserved antigens provide broader protection. Influenza matrix protein 2 (M2) is highly conserved across influenza A subtypes. To evaluate its efficacy as a vaccine candidate, we vaccinated mice with M2 peptide of a widely shared consensus sequence. This vaccination induced antibodies that cross-reacted with divergent M2 peptide from an H5N1 subtype. A DNA vaccine expressing full-length consensus-sequence M2 (M2-DNA) induced M2-specific antibody responses and protected against challenge with lethal influenza. Mice primed with M2-DNA and then boosted with recombinant adenovirus expressing M2 (M2-Ad) had enhanced antibody responses that cross-reacted with human and avian M2 sequences and induced T-cell responses. This M2 prime-boost vaccination conferred broad protection against challenge with lethal influenza A, including an H5N1 strain. Vaccination with M2, with key sequences represented, may provide broad protection against influenza A. |
format | Text |
id | pubmed-2725899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Centers for Disease Control and Prevention |
record_format | MEDLINE/PubMed |
spelling | pubmed-27258992009-09-10 Matrix Protein 2 Vaccination and Protection against Influenza Viruses, Including Subtype H5N1 Tompkins, Stephen Mark Zhao, Zi-Shan Lo, Chia-Yun Misplon, Julia A. Liu, Teresa Ye, Zhiping Hogan, Robert J. Wu, Zhengqi Benton, Kimberly A. Tumpey, Terrence M. Epstein, Suzanne L. Emerg Infect Dis Research Changes in influenza viruses require regular reformulation of strain-specific influenza vaccines. Vaccines based on conserved antigens provide broader protection. Influenza matrix protein 2 (M2) is highly conserved across influenza A subtypes. To evaluate its efficacy as a vaccine candidate, we vaccinated mice with M2 peptide of a widely shared consensus sequence. This vaccination induced antibodies that cross-reacted with divergent M2 peptide from an H5N1 subtype. A DNA vaccine expressing full-length consensus-sequence M2 (M2-DNA) induced M2-specific antibody responses and protected against challenge with lethal influenza. Mice primed with M2-DNA and then boosted with recombinant adenovirus expressing M2 (M2-Ad) had enhanced antibody responses that cross-reacted with human and avian M2 sequences and induced T-cell responses. This M2 prime-boost vaccination conferred broad protection against challenge with lethal influenza A, including an H5N1 strain. Vaccination with M2, with key sequences represented, may provide broad protection against influenza A. Centers for Disease Control and Prevention 2007-03 /pmc/articles/PMC2725899/ /pubmed/17552096 http://dx.doi.org/10.3201/eid1303.061125 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 | Research Tompkins, Stephen Mark Zhao, Zi-Shan Lo, Chia-Yun Misplon, Julia A. Liu, Teresa Ye, Zhiping Hogan, Robert J. Wu, Zhengqi Benton, Kimberly A. Tumpey, Terrence M. Epstein, Suzanne L. Matrix Protein 2 Vaccination and Protection against Influenza Viruses, Including Subtype H5N1 |
title | Matrix Protein 2 Vaccination and Protection against Influenza Viruses, Including Subtype H5N1 |
title_full | Matrix Protein 2 Vaccination and Protection against Influenza Viruses, Including Subtype H5N1 |
title_fullStr | Matrix Protein 2 Vaccination and Protection against Influenza Viruses, Including Subtype H5N1 |
title_full_unstemmed | Matrix Protein 2 Vaccination and Protection against Influenza Viruses, Including Subtype H5N1 |
title_short | Matrix Protein 2 Vaccination and Protection against Influenza Viruses, Including Subtype H5N1 |
title_sort | matrix protein 2 vaccination and protection against influenza viruses, including subtype h5n1 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2725899/ https://www.ncbi.nlm.nih.gov/pubmed/17552096 http://dx.doi.org/10.3201/eid1303.061125 |
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