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A single immunization with HA DNA vaccine by electroporation induces early protection against H5N1 avian influenza virus challenge in mice

BACKGROUND: Developing vaccines for the prevention of human infection by H5N1 influenza viruses is an urgent task. DNA vaccines are a novel alternative to conventional vaccines and should contribute to the prophylaxis of emerging H5N1 virus. In this study, we assessed whether a single immunization w...

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Detalles Bibliográficos
Autores principales: Zheng, Liyun, Wang, Fuyan, Yang, Zhongdong, Chen, Jianjun, Chang, Haiyan, Chen, Ze
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2652463/
https://www.ncbi.nlm.nih.gov/pubmed/19216752
http://dx.doi.org/10.1186/1471-2334-9-17
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author Zheng, Liyun
Wang, Fuyan
Yang, Zhongdong
Chen, Jianjun
Chang, Haiyan
Chen, Ze
author_facet Zheng, Liyun
Wang, Fuyan
Yang, Zhongdong
Chen, Jianjun
Chang, Haiyan
Chen, Ze
author_sort Zheng, Liyun
collection PubMed
description BACKGROUND: Developing vaccines for the prevention of human infection by H5N1 influenza viruses is an urgent task. DNA vaccines are a novel alternative to conventional vaccines and should contribute to the prophylaxis of emerging H5N1 virus. In this study, we assessed whether a single immunization with plasmid DNA expressing H5N1 hemagglutinin (HA) could provide early protection against lethal challenge in a mouse model. METHODS: Mice were immunized once with HA DNA at 3, 5, 7 days before a lethal challenge. The survival rate, virus titer in the lungs and change of body weight were assayed to evaluate the protective abilities of the vaccine. To test the humoral immune response induced by HA DNA, serum samples were collected through the eye canthus of mice on various days after immunization and examined for specific antibodies by ELISA and an HI assay. Splenocytes were isolated after the immunization to determine the antigen-specific T-cell response by the ELISPOT assay. RESULTS: Challenge experiments revealed that a single immunization of H5N1 virus HA DNA is effective in early protection against lethal homologous virus. Immunological analysis showed that an antigen-specific antibody and T-cell response could be elicited in mice shortly after the immunization. The protective abilities were correlated with the amount of injected DNA and the length of time after vaccination. CONCLUSION: A single immunization of 100 μg H5 HA DNA vaccine combined with electroporation was able to provide early protection in mice against homologous virus infection.
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spelling pubmed-26524632009-03-07 A single immunization with HA DNA vaccine by electroporation induces early protection against H5N1 avian influenza virus challenge in mice Zheng, Liyun Wang, Fuyan Yang, Zhongdong Chen, Jianjun Chang, Haiyan Chen, Ze BMC Infect Dis Research Article BACKGROUND: Developing vaccines for the prevention of human infection by H5N1 influenza viruses is an urgent task. DNA vaccines are a novel alternative to conventional vaccines and should contribute to the prophylaxis of emerging H5N1 virus. In this study, we assessed whether a single immunization with plasmid DNA expressing H5N1 hemagglutinin (HA) could provide early protection against lethal challenge in a mouse model. METHODS: Mice were immunized once with HA DNA at 3, 5, 7 days before a lethal challenge. The survival rate, virus titer in the lungs and change of body weight were assayed to evaluate the protective abilities of the vaccine. To test the humoral immune response induced by HA DNA, serum samples were collected through the eye canthus of mice on various days after immunization and examined for specific antibodies by ELISA and an HI assay. Splenocytes were isolated after the immunization to determine the antigen-specific T-cell response by the ELISPOT assay. RESULTS: Challenge experiments revealed that a single immunization of H5N1 virus HA DNA is effective in early protection against lethal homologous virus. Immunological analysis showed that an antigen-specific antibody and T-cell response could be elicited in mice shortly after the immunization. The protective abilities were correlated with the amount of injected DNA and the length of time after vaccination. CONCLUSION: A single immunization of 100 μg H5 HA DNA vaccine combined with electroporation was able to provide early protection in mice against homologous virus infection. BioMed Central 2009-02-12 /pmc/articles/PMC2652463/ /pubmed/19216752 http://dx.doi.org/10.1186/1471-2334-9-17 Text en Copyright ©2009 Zheng 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 Article
Zheng, Liyun
Wang, Fuyan
Yang, Zhongdong
Chen, Jianjun
Chang, Haiyan
Chen, Ze
A single immunization with HA DNA vaccine by electroporation induces early protection against H5N1 avian influenza virus challenge in mice
title A single immunization with HA DNA vaccine by electroporation induces early protection against H5N1 avian influenza virus challenge in mice
title_full A single immunization with HA DNA vaccine by electroporation induces early protection against H5N1 avian influenza virus challenge in mice
title_fullStr A single immunization with HA DNA vaccine by electroporation induces early protection against H5N1 avian influenza virus challenge in mice
title_full_unstemmed A single immunization with HA DNA vaccine by electroporation induces early protection against H5N1 avian influenza virus challenge in mice
title_short A single immunization with HA DNA vaccine by electroporation induces early protection against H5N1 avian influenza virus challenge in mice
title_sort single immunization with ha dna vaccine by electroporation induces early protection against h5n1 avian influenza virus challenge in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2652463/
https://www.ncbi.nlm.nih.gov/pubmed/19216752
http://dx.doi.org/10.1186/1471-2334-9-17
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