Cargando…
Induction of cross-protection against influenza A virus by DNA prime-intranasal protein boost strategy based on nucleoprotein
BACKGROUND: The highly conserved nucleoprotein (NP) is an internal protein of influenza virus and is capable of inducing cross-protective immunity against different influenza A viruses, making it a main target of universal influenza vaccine. In current study, we characterized the immune response ind...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511278/ https://www.ncbi.nlm.nih.gov/pubmed/23173785 http://dx.doi.org/10.1186/1743-422X-9-286 |
_version_ | 1782251572273610752 |
---|---|
author | Luo, Jian Zheng, Dan Zhang, Wenjie Fang, Fang Wang, Hanzhong Sun, Ying Ding, Yahong Xu, Chengfei Chen, Quanjiao Zhang, Hongbo Huang, Ding Sun, Bing Chen, Ze |
author_facet | Luo, Jian Zheng, Dan Zhang, Wenjie Fang, Fang Wang, Hanzhong Sun, Ying Ding, Yahong Xu, Chengfei Chen, Quanjiao Zhang, Hongbo Huang, Ding Sun, Bing Chen, Ze |
author_sort | Luo, Jian |
collection | PubMed |
description | BACKGROUND: The highly conserved nucleoprotein (NP) is an internal protein of influenza virus and is capable of inducing cross-protective immunity against different influenza A viruses, making it a main target of universal influenza vaccine. In current study, we characterized the immune response induced by DNA prime-intranasal protein boost strategy based on NP (A/PR/8/34, H1N1) in mouse model, and evaluated its protection ability against a lethal dose challenge of influenza virus. RESULTS: The intranasal boost with recombinant NP (rNP) protein could effectively enhance the pre-immune response induced by the NP DNA vaccine in mice. Compared to the vaccination with NP DNA or rNP protein alone, the prime-boost strategy increased the level of NP specific serum antibody, enhanced the T cell immune response, and relatively induced more mucosal IgA antibody. The overall immune response induced by this heterologous prime-boost regimen was Th-1-biased. Furthermore, the immune response in mice induced by this strategy provided not only protection against the homologous virus but also cross-protection against a heterosubtypic H9N2 strain. CONCLUSIONS: The NP DNA prime-intranasal protein boost strategy may provide an effective strategy for universal influenza vaccine development. |
format | Online Article Text |
id | pubmed-3511278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35112782012-12-01 Induction of cross-protection against influenza A virus by DNA prime-intranasal protein boost strategy based on nucleoprotein Luo, Jian Zheng, Dan Zhang, Wenjie Fang, Fang Wang, Hanzhong Sun, Ying Ding, Yahong Xu, Chengfei Chen, Quanjiao Zhang, Hongbo Huang, Ding Sun, Bing Chen, Ze Virol J Research BACKGROUND: The highly conserved nucleoprotein (NP) is an internal protein of influenza virus and is capable of inducing cross-protective immunity against different influenza A viruses, making it a main target of universal influenza vaccine. In current study, we characterized the immune response induced by DNA prime-intranasal protein boost strategy based on NP (A/PR/8/34, H1N1) in mouse model, and evaluated its protection ability against a lethal dose challenge of influenza virus. RESULTS: The intranasal boost with recombinant NP (rNP) protein could effectively enhance the pre-immune response induced by the NP DNA vaccine in mice. Compared to the vaccination with NP DNA or rNP protein alone, the prime-boost strategy increased the level of NP specific serum antibody, enhanced the T cell immune response, and relatively induced more mucosal IgA antibody. The overall immune response induced by this heterologous prime-boost regimen was Th-1-biased. Furthermore, the immune response in mice induced by this strategy provided not only protection against the homologous virus but also cross-protection against a heterosubtypic H9N2 strain. CONCLUSIONS: The NP DNA prime-intranasal protein boost strategy may provide an effective strategy for universal influenza vaccine development. BioMed Central 2012-11-23 /pmc/articles/PMC3511278/ /pubmed/23173785 http://dx.doi.org/10.1186/1743-422X-9-286 Text en Copyright ©2012 Luo 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 Luo, Jian Zheng, Dan Zhang, Wenjie Fang, Fang Wang, Hanzhong Sun, Ying Ding, Yahong Xu, Chengfei Chen, Quanjiao Zhang, Hongbo Huang, Ding Sun, Bing Chen, Ze Induction of cross-protection against influenza A virus by DNA prime-intranasal protein boost strategy based on nucleoprotein |
title | Induction of cross-protection against influenza A virus by DNA prime-intranasal protein boost strategy based on nucleoprotein |
title_full | Induction of cross-protection against influenza A virus by DNA prime-intranasal protein boost strategy based on nucleoprotein |
title_fullStr | Induction of cross-protection against influenza A virus by DNA prime-intranasal protein boost strategy based on nucleoprotein |
title_full_unstemmed | Induction of cross-protection against influenza A virus by DNA prime-intranasal protein boost strategy based on nucleoprotein |
title_short | Induction of cross-protection against influenza A virus by DNA prime-intranasal protein boost strategy based on nucleoprotein |
title_sort | induction of cross-protection against influenza a virus by dna prime-intranasal protein boost strategy based on nucleoprotein |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511278/ https://www.ncbi.nlm.nih.gov/pubmed/23173785 http://dx.doi.org/10.1186/1743-422X-9-286 |
work_keys_str_mv | AT luojian inductionofcrossprotectionagainstinfluenzaavirusbydnaprimeintranasalproteinbooststrategybasedonnucleoprotein AT zhengdan inductionofcrossprotectionagainstinfluenzaavirusbydnaprimeintranasalproteinbooststrategybasedonnucleoprotein AT zhangwenjie inductionofcrossprotectionagainstinfluenzaavirusbydnaprimeintranasalproteinbooststrategybasedonnucleoprotein AT fangfang inductionofcrossprotectionagainstinfluenzaavirusbydnaprimeintranasalproteinbooststrategybasedonnucleoprotein AT wanghanzhong inductionofcrossprotectionagainstinfluenzaavirusbydnaprimeintranasalproteinbooststrategybasedonnucleoprotein AT sunying inductionofcrossprotectionagainstinfluenzaavirusbydnaprimeintranasalproteinbooststrategybasedonnucleoprotein AT dingyahong inductionofcrossprotectionagainstinfluenzaavirusbydnaprimeintranasalproteinbooststrategybasedonnucleoprotein AT xuchengfei inductionofcrossprotectionagainstinfluenzaavirusbydnaprimeintranasalproteinbooststrategybasedonnucleoprotein AT chenquanjiao inductionofcrossprotectionagainstinfluenzaavirusbydnaprimeintranasalproteinbooststrategybasedonnucleoprotein AT zhanghongbo inductionofcrossprotectionagainstinfluenzaavirusbydnaprimeintranasalproteinbooststrategybasedonnucleoprotein AT huangding inductionofcrossprotectionagainstinfluenzaavirusbydnaprimeintranasalproteinbooststrategybasedonnucleoprotein AT sunbing inductionofcrossprotectionagainstinfluenzaavirusbydnaprimeintranasalproteinbooststrategybasedonnucleoprotein AT chenze inductionofcrossprotectionagainstinfluenzaavirusbydnaprimeintranasalproteinbooststrategybasedonnucleoprotein |