| Literature DB >> 29576303 |
Sanhua Wei7, Yingfeng Lei2, Jie Yang3, Xiaoyan Wang1, Fang Shu4, Xin Wei5, Fang Lin1, Bin Li1, Ying Cui1, Hai Zhang6, Sanhua Wei7.
Abstract
Hepatitis C virus (HCV) infection is a major public health problem despite effectual direct-acting antivirals (DAAs) therapy. Development of a prophylactic vaccine is essential to block spread of HCV infection. The HBV small surface antigen (HBsAg-S) can self-assemble into virus-like particles (VLPs), has higher immunogenicity and is used as a vaccine against HBV infections. Chimeric HBsAg-S proteins with foreign epitopes allow VLP formation and induce the specific humoral and cellular immune responses against the foreign proteins. In this study, we investigated the immune responses induced by chimeric VLPs with HCV neutralizing epitopes and HBV S antigen in mice. The chimeric HCV-HBV VLPs expressing neutralizing epitopes were prepared and purified. BALB/c mice were immunized with purified chimeric VLPs and the serum neutralizing antibodies were analyzed. We found that these chimeric VLPs induced neutralizing antibodies against HCV in mice. Additionally, the murine serum neutralized infections with HCV pseudoparticles and cell-cultured viruses derived from different heterologous 1a, 1b and 2a genotypes. We also found that immunization with chimeric VLPs induced anti-HBsAg antibodies. This study provides a novel strategy for development of a HCV prophylactic neutralizing epitope vaccine and a HCV-HBV bivalent prophylactic vaccine.Entities:
Keywords: Epitopes; Hepatitis C virus; Neutralizing antibody; Vaccine; Viral-like particles
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Year: 2018 PMID: 29576303 DOI: 10.1016/j.vaccine.2018.03.036
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641