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Oral immunization with recombinant enterovirus 71 VP1 formulated with chitosan protects mice against lethal challenge
BACKGROUND: Enterovirus 71 (EV71) is the etiologic agent of hand-foot-and-mouth disease (HFMD) in the Asia-Pacific region, Many strategies have been applied to develop EV71 vaccines but no vaccines are currently available. Mucosal immunization of the VP1, a major immunogenic capsid protein of EV71,...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022980/ https://www.ncbi.nlm.nih.gov/pubmed/24885121 http://dx.doi.org/10.1186/1743-422X-11-80 |
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author | Zhang, Fushun Hao, Chunsheng Zhang, Shuo Li, Aqian Zhang, Quanfu Wu, Wei Liu, Lin Li, Chuan Liang, Mifang Li, Xiuling Li, Dexin |
author_facet | Zhang, Fushun Hao, Chunsheng Zhang, Shuo Li, Aqian Zhang, Quanfu Wu, Wei Liu, Lin Li, Chuan Liang, Mifang Li, Xiuling Li, Dexin |
author_sort | Zhang, Fushun |
collection | PubMed |
description | BACKGROUND: Enterovirus 71 (EV71) is the etiologic agent of hand-foot-and-mouth disease (HFMD) in the Asia-Pacific region, Many strategies have been applied to develop EV71 vaccines but no vaccines are currently available. Mucosal immunization of the VP1, a major immunogenic capsid protein of EV71, may be an alternative way to prevent EV71 infection. RESULTS: In this study, mucosal immunogenicity and protect function of recombinant VP1 protein (rVP1) in formulation with chitosan were tested and assessed in female ICR mouse model. The results showed that the oral immunization with rVP1 induced VP1-specific IgA antibodies in intestine, feces, vagina, and the respiratory tract and serum-specific IgG and neutralization antibodies in vaccinated mice. Splenocytes from rVP1-immunized mice induced high levels of Th1 (cytokine IFN-γ), Th2 (cytokine IL-4) and Th3 (cytokine TGF-β) type immune responses after stimulation. Moreover, rVP1-immunized mother mice conferred protection (survival rate up to 30%) on neonatal mice against a lethal challenge of 10(3) plaque-forming units (PFU) EV71. CONCLUSIONS: These data indicated that oral immunization with rVP1 in formulation with chitosan was effective in inducing broad-spectrum immune responses and might be a promising subunit vaccine candidate for preventing EV71 infection. |
format | Online Article Text |
id | pubmed-4022980 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40229802014-05-17 Oral immunization with recombinant enterovirus 71 VP1 formulated with chitosan protects mice against lethal challenge Zhang, Fushun Hao, Chunsheng Zhang, Shuo Li, Aqian Zhang, Quanfu Wu, Wei Liu, Lin Li, Chuan Liang, Mifang Li, Xiuling Li, Dexin Virol J Research BACKGROUND: Enterovirus 71 (EV71) is the etiologic agent of hand-foot-and-mouth disease (HFMD) in the Asia-Pacific region, Many strategies have been applied to develop EV71 vaccines but no vaccines are currently available. Mucosal immunization of the VP1, a major immunogenic capsid protein of EV71, may be an alternative way to prevent EV71 infection. RESULTS: In this study, mucosal immunogenicity and protect function of recombinant VP1 protein (rVP1) in formulation with chitosan were tested and assessed in female ICR mouse model. The results showed that the oral immunization with rVP1 induced VP1-specific IgA antibodies in intestine, feces, vagina, and the respiratory tract and serum-specific IgG and neutralization antibodies in vaccinated mice. Splenocytes from rVP1-immunized mice induced high levels of Th1 (cytokine IFN-γ), Th2 (cytokine IL-4) and Th3 (cytokine TGF-β) type immune responses after stimulation. Moreover, rVP1-immunized mother mice conferred protection (survival rate up to 30%) on neonatal mice against a lethal challenge of 10(3) plaque-forming units (PFU) EV71. CONCLUSIONS: These data indicated that oral immunization with rVP1 in formulation with chitosan was effective in inducing broad-spectrum immune responses and might be a promising subunit vaccine candidate for preventing EV71 infection. BioMed Central 2014-05-06 /pmc/articles/PMC4022980/ /pubmed/24885121 http://dx.doi.org/10.1186/1743-422X-11-80 Text en Copyright © 2014 Zhang 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 credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Zhang, Fushun Hao, Chunsheng Zhang, Shuo Li, Aqian Zhang, Quanfu Wu, Wei Liu, Lin Li, Chuan Liang, Mifang Li, Xiuling Li, Dexin Oral immunization with recombinant enterovirus 71 VP1 formulated with chitosan protects mice against lethal challenge |
title | Oral immunization with recombinant enterovirus 71 VP1 formulated with chitosan protects mice against lethal challenge |
title_full | Oral immunization with recombinant enterovirus 71 VP1 formulated with chitosan protects mice against lethal challenge |
title_fullStr | Oral immunization with recombinant enterovirus 71 VP1 formulated with chitosan protects mice against lethal challenge |
title_full_unstemmed | Oral immunization with recombinant enterovirus 71 VP1 formulated with chitosan protects mice against lethal challenge |
title_short | Oral immunization with recombinant enterovirus 71 VP1 formulated with chitosan protects mice against lethal challenge |
title_sort | oral immunization with recombinant enterovirus 71 vp1 formulated with chitosan protects mice against lethal challenge |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022980/ https://www.ncbi.nlm.nih.gov/pubmed/24885121 http://dx.doi.org/10.1186/1743-422X-11-80 |
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