| Literature DB >> 26051517 |
Zi-Min Tang1, Ming Tang2, Min Zhao2, Gui-Ping Wen2, Fan Yang1, Wei Cai2, Si-Ling Wang1, Zi-Zheng Zheng3, Ning-Shao Xia4.
Abstract
Hepatitis E virus (HEV) is a serious public health problem that causes acute hepatitis in humans and is primarily transmitted through fecal and oral routes. The major anti-HEV antibody responses are against conformational epitopes located in a.a. 459-606 of HEV pORF2. All reported neutralization epitopes are present on the dimer domain constructed by this peptide. While looking for a neutralizing monoclonal antibody (MAb)-recognized linear epitope, we found a novel neutralizing linear epitope (L2) located in a.a. 423-437 of pORF2. Moreover, epitope L2 is proved non-immunodominant in the HEV-infection process. Using the hepatitis B virus core protein (HBc) as a carrier to display this novel linear epitope, we show herein that this epitope could induce a neutralizing antibody response against HEV in mice and could protect rhesus monkeys from HEV infection. Collectively, our results showed a novel non-immunodominant linear neutralizing epitope of hepatitis E virus, which provided additional insight of HEV vaccine.Entities:
Keywords: Hepatitis E virus; Linear epitope; Neutralization; Nonimmunodominant; Vaccine
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Year: 2015 PMID: 26051517 DOI: 10.1016/j.vaccine.2015.05.065
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641