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An M2e-based synthetic peptide vaccine for influenza A virus confers heterosubtypic protection from lethal virus challenge
BACKGROUND: Vaccination is considered as the most effective preventive method to control influenza. The hallmark of influenza virus is the remarkable variability of its major surface glycoproteins, HA and NA, which allows the virus to evade existing anti-influenza immunity in the target population....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3716895/ https://www.ncbi.nlm.nih.gov/pubmed/23834899 http://dx.doi.org/10.1186/1743-422X-10-227 |
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author | Ma, Ji-Hong Yang, Fu-Ru Yu, Hai Zhou, Yan-Jun Li, Guo-Xin Huang, Meng Wen, Feng Tong, Guangzhi |
author_facet | Ma, Ji-Hong Yang, Fu-Ru Yu, Hai Zhou, Yan-Jun Li, Guo-Xin Huang, Meng Wen, Feng Tong, Guangzhi |
author_sort | Ma, Ji-Hong |
collection | PubMed |
description | BACKGROUND: Vaccination is considered as the most effective preventive method to control influenza. The hallmark of influenza virus is the remarkable variability of its major surface glycoproteins, HA and NA, which allows the virus to evade existing anti-influenza immunity in the target population. So it is necessary to develop a novel vaccine to control animal influenza virus. Also we know that the ectodomain of influenza matrix protein 2 (M2e) is highly conserved in animal influenza A viruses, so a vaccine based on the M2e could avoid several drawbacks of the traditional vaccines. In this study we designed a novel tetra-branched multiple antigenic peptide (MAP) based vaccine, which was constructed by fusing four copies of M2e to one copy of foreign T helper (Th) cell epitope, and then investigated its immune responses. RESULTS: Our results show that the M2e-MAP induced strong M2e-specific IgG antibody,which responses following 2 doses immunization in the presence of Freunds’ adjuvant. M2e-MAP vaccination limited viral replication substantially. Also it could attenuate histopathological damage in the lungs of challenged mice and counteracted weight loss. M2e-MAP-based vaccine protected immunized mice against the lethal challenge with PR8 virus. CONCLUSIONS: Based on these findings, M2e-MAP-based vaccine seemed to provide useful information for the research of M2e-based influenza vaccine. Also it show huge potential to study vaccines for other similarly viruses. |
format | Online Article Text |
id | pubmed-3716895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37168952013-07-20 An M2e-based synthetic peptide vaccine for influenza A virus confers heterosubtypic protection from lethal virus challenge Ma, Ji-Hong Yang, Fu-Ru Yu, Hai Zhou, Yan-Jun Li, Guo-Xin Huang, Meng Wen, Feng Tong, Guangzhi Virol J Research BACKGROUND: Vaccination is considered as the most effective preventive method to control influenza. The hallmark of influenza virus is the remarkable variability of its major surface glycoproteins, HA and NA, which allows the virus to evade existing anti-influenza immunity in the target population. So it is necessary to develop a novel vaccine to control animal influenza virus. Also we know that the ectodomain of influenza matrix protein 2 (M2e) is highly conserved in animal influenza A viruses, so a vaccine based on the M2e could avoid several drawbacks of the traditional vaccines. In this study we designed a novel tetra-branched multiple antigenic peptide (MAP) based vaccine, which was constructed by fusing four copies of M2e to one copy of foreign T helper (Th) cell epitope, and then investigated its immune responses. RESULTS: Our results show that the M2e-MAP induced strong M2e-specific IgG antibody,which responses following 2 doses immunization in the presence of Freunds’ adjuvant. M2e-MAP vaccination limited viral replication substantially. Also it could attenuate histopathological damage in the lungs of challenged mice and counteracted weight loss. M2e-MAP-based vaccine protected immunized mice against the lethal challenge with PR8 virus. CONCLUSIONS: Based on these findings, M2e-MAP-based vaccine seemed to provide useful information for the research of M2e-based influenza vaccine. Also it show huge potential to study vaccines for other similarly viruses. BioMed Central 2013-07-09 /pmc/articles/PMC3716895/ /pubmed/23834899 http://dx.doi.org/10.1186/1743-422X-10-227 Text en Copyright ©2013 Ma et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Ma, Ji-Hong Yang, Fu-Ru Yu, Hai Zhou, Yan-Jun Li, Guo-Xin Huang, Meng Wen, Feng Tong, Guangzhi An M2e-based synthetic peptide vaccine for influenza A virus confers heterosubtypic protection from lethal virus challenge |
title | An M2e-based synthetic peptide vaccine for influenza A virus confers heterosubtypic protection from lethal virus challenge |
title_full | An M2e-based synthetic peptide vaccine for influenza A virus confers heterosubtypic protection from lethal virus challenge |
title_fullStr | An M2e-based synthetic peptide vaccine for influenza A virus confers heterosubtypic protection from lethal virus challenge |
title_full_unstemmed | An M2e-based synthetic peptide vaccine for influenza A virus confers heterosubtypic protection from lethal virus challenge |
title_short | An M2e-based synthetic peptide vaccine for influenza A virus confers heterosubtypic protection from lethal virus challenge |
title_sort | m2e-based synthetic peptide vaccine for influenza a virus confers heterosubtypic protection from lethal virus challenge |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3716895/ https://www.ncbi.nlm.nih.gov/pubmed/23834899 http://dx.doi.org/10.1186/1743-422X-10-227 |
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