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Long-term hepatitis B vaccine in infants born to hepatitis B e antigen positive mothers
Y Poovorawan1, S Sanpavat, S Chumdermpadetsuk
1Viral Hepatitis Research Unit Chulalongkorn University Hospital, Bangkok, Thailand.
Insights
This study shows recombinant hepatitis B vaccine provides excellent protection against chronic hepatitis B infection in high-risk neonates. A booster dose at 5-6 or 11-12 years may further reduce viral transmission.
Area of Science:
- Hepatology
- Immunology
- Pediatrics
Background:
- Hepatitis B virus (HBV) infection poses a significant risk to neonates born to infected mothers.
- Effective vaccination strategies are crucial for preventing chronic HBV carriage and associated liver disease.
Purpose of the Study:
- To evaluate the long-term efficacy of a recombinant hepatitis B vaccine in high-risk neonates.
- To assess the impact of a booster dose on sustained antibody levels and protection against HBV infection.
Main Methods:
- Neonates born to HBsAg and HBeAg positive mothers received a 10 µg recombinant hepatitis B vaccine at different primary immunization schedules (0, 1, 6 months or 0, 1, 2, 12 months).
- Participants were monitored for hepatitis B serological markers (HBsAg, anti-HBc, anti-HBs) up to 8 years of age.
- A subset received a booster dose at 60 months; re-exposure markers were analyzed after this period.
Main Results:
- Overall vaccine protection against HBsAg carriage reached 96.2% at 12 months.
- No child developed chronic carriage beyond 3 years of age, indicating immediate and long-term protection.
- Re-emergence of HBV markers without disease was comparable in boosted and non-boosted groups after 60 months.
Conclusions:
- The recombinant hepatitis B vaccine offers robust, long-term protection against chronic carriage and infection in high-risk neonates.
- A booster dose at 5-6 or 11-12 years is recommended to reduce HBV infection, viral circulation, and transmission, ensuring sustained antibody persistence.
Abstract:
Neonates of hepatitis B surface antigen (HBsAg) positive and hepatitis B encoded antigen (HBeAg) positive mothers received 10 micrograms of recombinant hepatitis B vaccine at months 0, 1, 6, or 0, 1, 2, 12, with or without immunoglobulin at birth, and were followed up to the age of 8 years for HBsAg, anti-HBc, and anti-HBs. Some were boosted at month 60. The overall vaccine protection at month 12 was 96.2%. No child became a chronic carrier beyond the age of 3 years, showing that this vaccine provides immediate protection against HBsAg carriage, and long term protection against fetally acquired HBsAg. After month 60 hepatitis B serological markers without disease, indicating re-exposure to HBV, reappeared in comparable numbers among boosted and non-boosted children (5 for a total of 167 children). This vaccine provides long-term protection against hepatitis B chronic carriage and infection in high risk neonates with or without a month 60 booster. A booster at the age of 5-6 years or 11-12 years would reduce HBV infection, viral circulation and transmission, while ensuring long-term antibody persistence.
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