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Published on: September 25, 2019
Long-term immunogenicity and efficacy of universal hepatitis B virus vaccination in Taiwan
Yu-Cheng Lin1, Mei-Hwei Chang, Yen-Hsuan Ni
1Department of Pediatrics, National Taiwan University Hospital and National Taiwan University, College of Medicine, Taipei, Taiwan.
Insights
Long-term hepatitis B virus (HBV) vaccine immunogenicity in adolescents shows protective antibody levels wane but chronic infection remains rare. Routine booster vaccination may not be necessary before age 15.
Area of Science:
- Immunology
- Vaccinology
- Public Health
Background:
- The long-term immunogenicity of universal hepatitis B virus (HBV) vaccination, particularly in adolescents, is not well-documented.
- Understanding vaccine effectiveness over time is crucial for public health strategies.
Purpose of the Study:
- To assess the long-term immunogenicity and protective antibody levels of the universal HBV vaccine in adolescents.
- To evaluate the necessity of routine booster vaccinations in preventing chronic HBV infection.
Main Methods:
- A prospective community-based study followed 1200 children from age 7 to 14 years.
- Annual assessment of HBV surface antigen (HBsAg), anti-HBs, and anti-HBc levels.
- Comparison of outcomes between children who received booster vaccinations and those who did not.
Main Results:
- Eleven children showed evidence of new HBV infection (anti-HBc positive), but none developed HBsAg positivity or detectable HBV DNA.
- Protective anti-HBs levels decreased from 71.1% at age 7 to 37.4% at age 12 in non-boosted children.
- New anti-HBc positivity was rare in both booster (1/200) and non-booster (2/258) groups.
Conclusions:
- Hepatitis B virus vaccine provides sustained protection against chronic infection in adolescents, even as antibody levels decline.
- Routine booster vaccination does not appear necessary for preventing chronic HBV infection before age 15.
Abstract:
The long-term immunogenicity of universal hepatitis B virus (HBV) vaccine is seldom studied in large-scale prospective community-based populations, especially in adolescents. This study enrolled 1200 children aged 7 years with complete HBV immunization in infancy and determined HBV surface antigen (HBsAg), its antibody (anti-HBs), and HBV core antibody (anti-HBc) annually until the children were aged 14 years. Eleven children had new HBV infections with anti-HBc positivity as the only marker. None became positive for HBsAg or had detectable HBV DNA by polymerase chain reaction. The percentage of protective anti-HBs in 951 children without booster vaccination gradually decreased from 71.1% at age 7 years to 37.4% at age 12 years. Only 1 of the 200 children in the booster group and 2 of the 258 children in the nonbooster group developed new anti-HBc positivity. The results suggest that routine booster vaccination may not be required to provide protection against chronic HBV infection before age 15 years.
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