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Persistence of long-term immunity to hepatitis B among adolescents immunized at birth
Sandra S Chaves1, Gayle Fischer, Justina Groeger
1Centers for Disease Control and Prevention, Atlanta, GA 30333, USA. schaves@cdc.gov
Insights
Long-term immunity from hepatitis B vaccination in childhood is generally strong, with most individuals retaining protection 15 years later. However, some may require revaccination if exposed to the hepatitis B virus.
Area of Science:
- Immunology
- Vaccinology
- Public Health
Background:
- The duration of immunity following recombinant hepatitis B vaccination initiated at birth is not fully understood.
- Waning immunity may increase young adults' risk of hepatitis B virus infection from occupational or behavioral exposures.
Purpose of the Study:
- To assess the long-term persistence of protection conferred by a recombinant hepatitis B vaccine regimen (5 mcg, 2.5 mcg, 2.5 mcg) administered starting at birth.
- To evaluate the anamnestic response to a booster dose at 10 and 15 years post-vaccination as a measure of immune memory.
Main Methods:
- A cohort of children vaccinated from birth with a 3-dose recombinant hepatitis B vaccine was followed.
- Participants received a booster dose 10 and 15 years after primary vaccination.
- Anamnestic response to the booster dose was measured to assess immune memory persistence.
Main Results:
- Over 70% of participants who lost protective antibody levels demonstrated an anamnestic response to the booster dose.
- Response rates to the booster remained stable between the 10 and 15-year follow-up points.
- A high initial antibody concentration post-primary vaccination correlated with a sustained anamnestic response; however, 20-30% failed to mount an immune response after boosting.
Conclusions:
- Recombinant hepatitis B vaccination initiated at birth generally provides durable protection, evidenced by robust anamnestic responses 15 years later.
- Hepatitis B revaccination may be necessary for individuals vaccinated from birth if they face ongoing exposure risks.
- Future recommendations should consider studies evaluating protection against clinically significant hepatitis B disease.
Abstract:
The long-term duration of recombinant hepatitis B vaccine-induced immunity among persons vaccinated starting at birth is still not well understood. Waning of vaccine-induced immunity could leave young adults at risk of hepatitis B virus infection due to behavioral or occupational exposures. We followed a cohort of children immunized starting at birth with a 3-dose regimen of recombinant hepatitis B vaccine (5 mcg, 2.5 mcg, 2.5 mcg). They were challenged with a booster dose of the hepatitis B vaccine 10 and 15 years after vaccination to assess anamnestic response as a measure of persistence of protection. Among 108 participants who had lost protective antibody levels against hepatitis B, the majority (>70%) had an anamnestic response to the booster dose; response rates did not decline significantly between 10 and 15 years follow-up periods. A high antibody concentration following primary vaccination was independently associated with an anamnestic response later on in life. Nonetheless, ~20-30% of participants were unable to mount an immune response after boosting. Hepatitis B revaccination might be required for persons vaccinated starting at birth if opportunities for hepatitis B virus exposure exist. Future vaccine recommendations should be based on studies ascertaining protection against clinically significant disease.
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