Frontiers in Microbiology (Mar 2024)

Multi-epitope vaccine design for hepatitis E virus based on protein ORF2 and ORF3

  • Qiong Lu,
  • Hao Wu,
  • Hao Wu,
  • Jing Meng,
  • Jiangyuan Wang,
  • Jiajing Wu,
  • Shuo Liu,
  • Shuo Liu,
  • Jincheng Tong,
  • Jianhui Nie,
  • Weijin Huang

DOI
https://doi.org/10.3389/fmicb.2024.1372069
Journal volume & issue
Vol. 15

Abstract

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IntroductionHepatitis E virus (HEV), with heightened virulence in immunocompromised individuals and pregnant women, is a pervasive threat in developing countries. A globaly available vaccine against HEV is currently lacking.MethodsWe designed a multi-epitope vaccine based on protein ORF2 and ORF3 of HEV using immunoinformatics.ResultsThe vaccine comprised 23 nontoxic, nonallergenic, soluble peptides. The stability of the docked peptide vaccine-TLR3 complex was validated by molecular dynamic simulations. The induction of effective cellular and humoral immune responses by the multi-peptide vaccine was verified by simulated immunization.DiscussionThese findings provide a foundation for future HEV vaccine studies.

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