Abstract
Hepatitis E virus (HEV) infection causes sporadic outbreaks of acute hepatitis worldwide. HEV was previously considered to be restricted to resource-limited countries with poor sanitary conditions, but increasing evidence implies that HEV is also a public health problem in developed countries and regions. Fortunately, several vaccine candidates based on virus-like particles (VLPs) have progressed into the clinical development stage, and one of them has been approved in China. This review provides an overview of the current HEV vaccine pipeline and future development with the emphasis on defining the critical quality attributes for the well-characterized vaccines. The presence of clinically relevant epitopes on the VLP surface is critical for eliciting functional antibodies against HEV infection, which is the key to the mechanism of action of the prophylactic vaccines against viral infections. Therefore, the epitope-specific immunochemical assays based on monoclonal antibodies (mAbs) for HEV vaccine antigen are critical methods in the toolbox for epitope characterization and for in vitro potency assessment. Moreover, serological evaluation methods after immunization are also discussed as biomarkers for clinical performance. The vaccine efficacy surrogate assays are critical in the preclinical and clinical stages of VLP-based vaccine development.
Highlights
Hepatitis E virus (HEV) belongs to the genus Orthohepevirus within the family Hepeviridae
We focus on epitope-specific antigenic analyses of hepatitis E vaccine antigen and evaluation assays of vaccine-elicited functional antibodies for its overall neutralization activity or against well-characterized epitopes
Prophylactic vaccination is an effective method to protect against HEV infection and control
Summary
Hepatitis E virus (HEV) belongs to the genus Orthohepevirus within the family Hepeviridae. HEV was recently found to be a quasi-enveloped virus It exists as non-enveloped virions in faeces and urine for transmission, whereas its form could be predominantly enveloped in serum for evading neutralizing antibodies [17,18,19]. VLPs could be more virion-like, including the size and the array of the epitope, while others could be smaller in size and less regular in particle formation, which are essential for effectively stimulating the immune response. Among these truncated pORF2 molecules, three vaccine candidates have been studied in clinical trials. We focus on epitope-specific antigenic analyses of hepatitis E vaccine antigen and evaluation assays of vaccine-elicited functional antibodies for its overall neutralization activity or against well-characterized epitopes
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