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Absence or delayed appearance of hepatitis B core antibody in chronic hepatitis B surface antigen carrier children

Y H Ni1, H Y Hsu, M H Chang

  • 1Department of Pediatrics, College of Medicine, National Taiwan University, Taipei, Republic of China.

Journal of Hepatology
|February 1, 1993
PubMed

Insights

In children carrying the hepatitis B surface antigen (HBsAg), the hepatitis B core antibody (anti-HBc) sometimes fails to appear or is delayed, particularly in those infected perinatally. This study followed 420 HBsAg carrier children to investigate anti-HBc development.

Area of Science:

  • Hepatology
  • Virology
  • Immunology

Background:

  • Hepatitis B virus (HBV) infection can lead to chronic carriage.
  • The role and timing of hepatitis B core antibody (anti-HBc) development in HBsAg carrier children are not fully understood.

Purpose of the Study:

  • To investigate the longitudinal development of anti-HBc in children who are hepatitis B surface antigen (HBsAg) carriers.
  • To identify factors associated with the absence or delayed appearance of anti-HBc.

Main Methods:

  • Longitudinal follow-up of 420 HBsAg carrier children.
  • Serological testing for HBsAg, HBeAg, and anti-HBc.
  • Hepatitis B virus DNA (HBV-DNA) quantification.
  • Liver biopsy in select cases.

Main Results:

  • 10 (2.4%) children showed absence or delayed anti-HBc appearance.
  • Absence of anti-HBc occurred in 4 children, including one with hepatitis B vaccine failure and three born to HBsAg carrier mothers.
  • Delayed anti-HBc appearance (2-8 years) was observed in 6 children, all born to HBsAg carrier mothers.
  • High HBV replication (HBsAg and HBV-DNA) was noted in all 10 children.
  • Absence of anti-HBc was strongly associated with perinatal infection.

Conclusions:

  • The absence or delayed appearance of anti-HBc is uncommon in HBsAg carrier children but is linked to high HBV replication and perinatal infection.
  • Further investigation is needed to understand the long-term implications of absent or delayed anti-HBc in this population.

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