Development and evaluation of two subunit vaccine candidates containing antigens of hepatitis E virus, rotavirus, and astrovirus
dc.contributor.author | Xia, Ming | en |
dc.contributor.author | Wei, Chao | en |
dc.contributor.author | Wang, Leyi | en |
dc.contributor.author | Cao, Dianjun | en |
dc.contributor.author | Meng, Xiang-Jin | en |
dc.contributor.author | Jiang, Xi | en |
dc.contributor.author | Tan, Ming | en |
dc.date.accessioned | 2019-01-23T14:27:29Z | en |
dc.date.available | 2019-01-23T14:27:29Z | en |
dc.date.issued | 2016-05-19 | en |
dc.description.abstract | Hepatitis E virus (HEV), rotavirus (RV), and astrovirus (AstV) are important pathogens that transmit through a common fecal-oral route, causing hepatitis (HEV) and gastroenteritis (RV and AstV) respectively in humans. In this study, we developed and evaluated two subunit vaccine candidates that consisted of the same protruding or spike protein antigens of the three viruses in two formats, a fusion of the three antigens into one molecule (fused vaccine) vs. a mixture of the three free antigens together (mixed vaccine). Both vaccines were easily made via E. coli expression system. Mouse immunization experiments showed that the fused vaccine elicited significantly higher antibody responses against the three viral antigens than those induced by the mixed vaccine. In addition, the mouse post-immune antisera of the fused vaccine revealed significantly higher neutralizing titers against HEV infection in cell culture, as well as significantly higher 50% blocking titers (BT50) against RV VP8-HBGA receptor interactions than those of the post-immune antisera after immunization of the mixed vaccine. Thus, the fused vaccine is a promising trivalent vaccine candidate against HEV, RV, and AstV, which is worth for further development. | en |
dc.description.notes | The research described in this article was supported by the National Institute of Health, the National Institute of Allergy and Infectious Diseases (5R01 AI089634-01 to X.J. and R21 AI092434-01A1 to M.T.) and an institutional Innovation Fund of Cincinnati Children's Hospital Medical Center to M.T. | en |
dc.description.sponsorship | National Institute of Health; National Institute of Allergy and Infectious Diseases [5R01 AI089634-01, R21 AI092434-01A1]; institutional Innovation Fund of Cincinnati Children's Hospital Medical Center | en |
dc.format.extent | 12 | en |
dc.format.mimetype | application/pdf | en |
dc.identifier.doi | https://doi.org/10.1038/srep25735 | en |
dc.identifier.issn | 2045-2322 | en |
dc.identifier.other | 25735 | en |
dc.identifier.pmid | 27194006 | en |
dc.identifier.uri | http://hdl.handle.net/10919/86849 | en |
dc.identifier.volume | 6 | en |
dc.language.iso | en | en |
dc.publisher | Springer Nature | en |
dc.rights | Creative Commons Attribution 4.0 International | en |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | en |
dc.subject | blood group antigens | en |
dc.subject | capsid protein forms | en |
dc.subject | intussusception risk | en |
dc.subject | united-states | en |
dc.subject | p-domain | en |
dc.subject | norovirus | en |
dc.subject | particle | en |
dc.subject | neutralization | en |
dc.subject | receptors | en |
dc.subject | mortality | en |
dc.title | Development and evaluation of two subunit vaccine candidates containing antigens of hepatitis E virus, rotavirus, and astrovirus | en |
dc.title.serial | Scientific Reports | en |
dc.type | Article - Refereed | en |
dc.type.dcmitype | Text | en |
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