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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...

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Detalles Bibliográficos
Autores principales: 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.
Formato: Texto
Lenguaje:English
Publicado: Centers for Disease Control and Prevention 2007
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
Descripción
Sumario: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.