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Hepatitis B vaccination in children: five year booster study
A Milne1, S Krugman, J A Waldon
1Hepatitis Research Unit, Whakatane, New Zealand.
Insights
Hepatitis B vaccination in children provides protection for at least five years. Booster doses are not needed within this timeframe if initial vaccine response is strong, aiding hepatitis B control in endemic regions.
Area of Science:
- Immunology
- Vaccinology
- Pediatrics
Background:
- Hepatitis B virus (HBV) infection is a significant global health concern, particularly in endemic areas.
- Effective vaccination strategies are crucial for controlling HBV transmission in pediatric populations.
Purpose of the Study:
- To assess the duration of protective immunity conferred by hepatitis B vaccines in children.
- To determine the necessity of booster doses within five years post-primary immunization.
Main Methods:
- A cohort of 318 children received a 2-microgram intramuscular dose of recombinant DNA vaccine (rDNAV).
- These children had previously received plasma-derived vaccine (PDV) doses five years prior.
- Hepatitis B virus (HBV) seromarkers were analyzed pre- and post-booster administration.
Main Results:
- All children demonstrated an anamnestic response to the booster dose.
- The geometric mean titre (GMT) of antibody to hepatitis B surface antigen (antiHBs) significantly increased from 89 to 4777 IU/L.
- Antibody detection rates were high, with 94% positive before the booster and 96.5% positive shortly after.
Conclusions:
- Satisfactory initial seroconversion indicates sustained protection for at least five years.
- Booster doses for hepatitis B are not required for children within five years if primary immunization is successful.
- These findings support simplified hepatitis B vaccination schedules for population control in endemic regions.
Aim:
to demonstrate that appropriate doses of hepatitis B vaccines would be protective for at least five years in children. This would be shown by administering booster doses and measuring the response.
Methods:
2 micrograms intramuscular (IM) doses of Merck Sharp and Dohme (MSD) recombinant DNA vaccine (rDNAV) were given to 318 children who had received age appropriate doses of MSD plasma derived vaccine (PDV) five years earlier. Sera were tested for hepatitis B virus (HBV) seromarkers pre- and postbooster.
Results:
all children who had responsed to primary immunisation demonstrated an anamnestic response. The geometric mean titre (GMT) of antibody to hepatitis B surface antigen (antiHBs) rose from 89 to 4777 IU/L. AntiHBs was detected in 94% of vaccinees just prior to the five year booster, and 96.5% a mean of 10 days later.
Conclusion:
when initial vaccine seroconversion is satisfactory, protection of responders persists for at least five years, assuming that the response to vaccine boosters mimics the response to wild virus. Therefore, for population control of hepatitis B in children in endemic areas, booster doses are not required for at least five years.
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