Evaluation of hepatitis E antigen kinetics and its diagnostic utility for prediction of the outcomes of hepatitis E virus genotype 1 infection

Virulence. 2021 Dec;12(1):1334-1344. doi: 10.1080/21505594.2021.1922027.

Abstract

HEV-Ag ELISA assay is a reliable diagnostic test in resource-limited areas. HEV genotype 1 (HEV-1) infections are either self-limited or progress to fulminant hepatic failure (FHF) and death if anti-HEV therapy is delayed. Limited data is available about the diagnostic utility of HEV Ag on HEV-1 infections. Herein wWe aimed to study the kinetics of HEV Ag during HEV-1 infections at different stages, i.e., acute HEV infection, recovery, and progression to FHF. Also, we evaluated the diagnostic utility of this marker to predict the outcomes of HEV-1 infections. Plasma of acute hepatitis E (AHE) patients were assessed for HEV RNA by RT-qPCR, HEV Ag, and anti-HEV IgM by ELISA. The kinetics of HEV Ag was monitored at different time points; acute phase of infection, recovery, FHF stage, and post-recovery. Our results showed that the level of HEV Ag was elevated in AHE patients with a significantly higher level in FHF patients than recovered patients. We identified a plasma HEV Ag threshold that can differentiate between self-limiting infection and FHF progression with 100% sensitivity and 88.89% specificity. HEV Ag and HEV RNA have similar kinetics during the acute phase and self-limiting infection. In the FHF stage, HEV Ag and anti-HEV IgM have similar patterns of kinetics which could be the cause of liver damage. In conclusion, the HEV Ag assay can be used as a biomarker for predicting the consequences of HEV-1 infections which could be diagnostically useful for taking the appropriate measures to reduce the complications, especially for high-risk groups.

Keywords: HEV antigen; HEV genotype 1; HEV kinetic; acute self-limiting infection; fulminant hepatic failure; predictive biomarker.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers
  • Genotype
  • Hepatitis Antibodies
  • Hepatitis Antigens / analysis*
  • Hepatitis E virus* / genetics
  • Hepatitis E* / diagnosis
  • Humans
  • Immunoglobulin M
  • Kinetics
  • RNA, Viral

Substances

  • Biomarkers
  • Hepatitis Antibodies
  • Hepatitis Antigens
  • Immunoglobulin M
  • RNA, Viral

Grants and funding

The grant office of Faculty of Medicine, Assiut University, Egypt (Grant ID 006‐27‐07‐2020).