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Long term antibody response to hepatitis B vaccination beginning at birth and to subsequent booster vaccination
Ian T Williams1, Susan T Goldstein, Joseph Tufa
1Division of Viral Hepatitis, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA 30030, USA. IWilliams@CDC.GOV
Insights
Hepatitis B vaccination in infancy provides lasting antibody protection. A booster dose at ages 5 or 9 elicits a strong response, confirming long-term immunity in children.
Area of Science:
- Immunology
- Vaccinology
- Pediatrics
Background:
- Limited data exist on long-term antibody persistence after infant hepatitis B vaccination.
- The response to booster doses in children vaccinated from birth requires further investigation.
Purpose of the Study:
- To assess long-term antibody persistence after infant hepatitis B vaccination.
- To evaluate the immunogenicity of a booster dose administered years after the primary series.
Main Methods:
- Two groups of children received either recombinant or plasma-derived hepatitis B vaccine at birth, 1, and 6 months.
- Booster doses were administered at age 5 (Group 1) or 9 (Group 2).
- Antibody levels and hepatitis B virus infection markers were monitored before and after booster vaccination, with follow-up up to one year.
Main Results:
- After the primary series, 90% of Group 1 children had protective antibody levels at 13 months.
- Before booster doses, protective antibody levels were found in 41% of Group 1 and 39% of Group 2.
- All children demonstrated an anamnestic response to the booster, with significant antibody declines observed one year post-booster.
Conclusions:
- Primary hepatitis B vaccination initiated at birth provides durable protection in children.
- Both plasma-derived and recombinant vaccines are effective in establishing long-term immunity.
- Booster doses effectively restore antibody levels in children with waning immunity.
Background:
Few studies have examined the long term persistence of antibody after hepatitis B immunization beginning at birth and the response to a subsequent challenge with a booster dose of vaccine.
Methods:
Two groups of children received hepatitis B vaccine on a schedule of birth and 1 and 6 months of age. Group 1 received recombinant vaccine and a booster dose at 5 years of age. Group 2 received plasma-derived vaccine and a booster dose at 9 years of age. Group 1 children were tested for antibody after the primary vaccine series. All children were tested for antibody before administration of the booster dose and at 2 and 4 weeks and 1 year after the booster. In addition all children were tested for markers of hepatitis B virus infection.
Results:
Antibody testing conducted after the primary series for children in Group 1 (n = 70) showed that 90% had protective antibody concentrations at 13 months of age, and testing before the booster dose showed that 41% had protective antibody concentrations. All children with protective antibody concentrations after the primary series had an anamnestic antibody response to the booster dose. In Group 2 (n = 41) 39% of children had protective antibody concentrations before the booster dose, and 93% had an anamnestic antibody response to the booster dose. One year after the booster dose there were 26-fold and 11-fold declines in antibody concentration in Groups 1 and 2, respectively.
Conclusions:
A primary vaccination series with either plasma-derived or recombinant hepatitis B vaccine affords long term protection for children when vaccinated beginning soon after birth.
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