Abstract

BackgroundIn occult hepatitis B viral infection (OBI), the persistence of hepatitis B virus (HBV) DNA is associated with a lack of hepatitis B surface antigen (HBsAg). To assess the possible role of HBsAg immune escape variants in OBI patients, variability in the HBV S gene was evaluated for OBI patients as well as chronic HBV infection patients from the same families.MethodsWe selected 17 HBV DNA-positive/HBsAg-negative patients (OBI group) and 15 HBV DNA- and HBsAg-positive patients from OBI families (control group). The S gene was amplified and cloned, and at least 15 clones per patient were sequenced and analyzed.ResultsAlthough the incidence of stop codon mutations within the S region was higher in the OBI group (13.6 %) than in the control group (1.5 %, P < 0.001), this type of mutation, together with insertion and deletion mutations, was prevalent in only three OBI patients. In the major hydrophilic region (MHR), a median of 0.75 residues were altered in every 100 residues for the OBI patients, whereas 0.95 out of 100 residues were changed in the control group (P = 0.428). Furthermore, some variants that are generally considered immune escape variants, such as mutations at positions s145, s147, and s123, were only observed in less than 5 % of all the clones sequenced, in either OBI or control group.ConclusionsOur data suggest that HBsAg variants may not play a major role in OBI pathogenesis.

Highlights

  • In occult hepatitis B viral infection (OBI), the persistence of hepatitis B virus (HBV) DNA is associated with a lack of hepatitis B surface antigen (HBsAg)

  • In order to explore the mechanisms underlying OBI, we investigated 17 of the patients diagnosed with OBI from 15 families (F1–F15) which include a member with chronic HBV infection

  • Of the samples collected from these families, 44 individuals were negative for HBsAg, among which 17 were diagnosed as OBI

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Summary

Introduction

In occult hepatitis B viral infection (OBI), the persistence of hepatitis B virus (HBV) DNA is associated with a lack of hepatitis B surface antigen (HBsAg). Several reports have described the persistence of HBV DNA in 0–76.2 % of HBsAg-negative patients [3,4,5,6,7]. This phenomenon, named occult hepatitis B infection (OBI), is defined as the presence of HBV DNA in the patient’s serum and/or hepatocytes, but a lack of serum HBsAg [8].

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