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Hepatitis B surface antigenemia at birth: a long-term follow-up study
1Department of Pediatrics, College of Medicine, National Taiwan University, Taipei.
The Journal of Pediatrics
|September 17, 1998
Summary
Current hepatitis B immunoprophylaxis fails to prevent newborns infected in utero from becoming carriers. Even with treatment, some children show immune responses against hepatitis B virus (HBV).
Area of Science:
- Hepatology
- Immunology
- Pediatrics
Background:
- Hepatitis B virus (HBV) infection poses a significant global health challenge.
- Maternal carriage of hepatitis B surface antigen (HBsAg) and hepatitis B e antigen (HBeAg) indicates a high risk of perinatal transmission.
- Current immunoprophylaxis aims to prevent HBV transmission from infected mothers to newborns.
Purpose of the Study:
- To determine the effectiveness of the current immunoprophylaxis program in preventing HBV infection in newborns born to HBeAg-positive HBsAg carrier mothers.
- To investigate the prevalence and long-term outcomes of hepatitis B surface antigenemia in these high-risk newborns.
Main Methods:
- A prospective cohort study involving 665 newborns born to HBeAg-positive HBsAg carrier mothers between 1984 and 1993.
- Newborns were tested for HBsAg shortly after birth, prior to receiving hepatitis B immune globulin and vaccination.
- Seropositive infants were monitored for HBV markers, liver function, and alpha-fetoprotein levels until 1996.
Main Results:
- Sixteen newborns (2.4%) were HBsAg-positive at birth and remained so at 6 months, indicating failure of immunoprophylaxis.
- All 12 infants who received long-term follow-up were confirmed chronic HBV carriers.
- Among the chronic carriers, some exhibited HBeAg seroconversion or alanine aminotransferase flares, while others showed delayed anti-HBc appearance.
Conclusions:
- The current immunoprophylaxis strategy is insufficient to prevent HBV infection in newborns with in utero acquired surface antigenemia.
- Despite immune tolerance, some chronically infected children may mount immune responses against HBV.
- Further strategies are needed to address HBV transmission in high-risk mother-infant pairs.