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Published on: September 25, 2019
Occult hepatitis B virus infection in immunized children born to carrier mothers
Koji Yokoyama1,2, Hideki Kumagai1, Masaharu Takahashi2
1Department of Pediatrics, Jichi Medical University School of Medicine, Shimotsuke, Tochigi, Japan.
Insights
Occult hepatitis B virus (HBV) infection (OBI) prevalence in immunoprophylaxis-treated children in Japan is low (1.3%). Close monitoring is crucial as OBI can progress to overt infection, even after treatment.
Area of Science:
- Hepatology
- Virology
- Pediatrics
Background:
- Occult hepatitis B virus infection (OBI) transmission from mothers to children (MTCT) despite immunoprophylaxis is poorly understood in Japan.
- This study aimed to determine OBI prevalence in Japanese children born to HBV carrier mothers and identify associated genomic mutations.
Observation:
- 158 children receiving passive-active immunoprophylaxis were analyzed for HBV markers and DNA.
- HBV genomes were sequenced to identify mutations.
- Three children experienced HBV MTCT: two with OBI (1.3%) and one with resolved HBV infection (RBI) (0.6%).
Findings:
- The HBV genomes in OBI cases were wild-type and identical to maternal strains.
- One child with OBI developed overt HBV infection after repeated hepatitis B immunoglobulin (HBIG) treatment, exhibiting an S gene G145R mutation potentially induced by HBIG.
- The child with RBI remained persistently positive for antibody to HBV core antigen.
Implications:
- A low prevalence of OBI was found in children receiving immunoprophylaxis in Japan.
- The progression of OBI to overt infection highlights the need for long-term monitoring in infants.
- Genomic analysis may reveal mutations influencing OBI pathogenesis and treatment response.
Background:
The prevalence of occult hepatitis B virus (HBV) infection (OBI) in children due to mother-to-child transmission (MTCT) despite immunoprophylaxis remains controversial and is still unknown in Japan. The aim of this study was to determine the OBI prevalence in such children in Japan and identify the genomic mutations that might be associated with the pathogenesis of OBI in children.
Methods:
The data on 158 children born to HBV carrier mothers and who received complete passive-active immunoprophylaxis after birth in 2002-2014 were reviewed. HBV markers were detected using commercial enzyme-linked immunosorbent assay kits. HBV-DNA was detected using real-time and nested polymerase chain reaction. Complete genomic sequences were determined.
Results:
Among the 158 children studied, three had HBV MTCT: two had OBI, and one had resolved HBV infection (RBI). The prevalence of OBI and RBI was estimated to be 1.3% and 0.6%, respectively. The HBV genomes of the two OBI children were wild type and 100% identical to those of their mothers. Of these two children, one received repeated hepatitis B immunoglobulin (HBIG) and developed overt HBV infection. Her HBV genome had a G145R mutation in the S gene that might have been induced by HBIG treatment. The RBI child was persistently positive for antibody to HBV core antigen (10-12 signal/cut-off ratio; S/CO).
Conclusions:
A low prevalence of OBI was observed in children who received immunoprophylaxis for preventing MTCT in Japan. The development of overt HBV infection in infants with OBI indicates the necessity of close and long-term monitoring.
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