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Strategies for hepatitis B booster vaccination among children: an 8-year prospective cohort study
Yan Qiu1, Jing-Jing Ren1, Zi-Kang Wu2
1State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, Zhejiang University , Hangzhou, China.
Insights
A 10 μg hepatitis B vaccine booster, administered on a 0-1-6 month schedule, provides robust and long-lasting protection in children. One booster dose may be sufficient for children with existing anti-HBs titers.
Area of Science:
- Immunology
- Vaccinology
- Pediatrics
Background:
- Universal infant hepatitis B vaccination is standard practice.
- Debate exists regarding the necessity and optimal strategy for booster doses in children.
- Assessing long-term antibody persistence and response to boosters is crucial for public health.
Purpose of the Study:
- To investigate the need for hepatitis B virus (HBV) booster vaccination in children.
- To evaluate different strategies for HBV booster vaccination.
- To determine the optimal dosage and schedule for booster responses.
Main Methods:
- An 8-year prospective cohort study involving 4170 children aged 5-15 years.
- Participants were grouped based on pre-booster anti-HBs antibody levels (<0.1, 0.1-<1, 1-<10 mIU/mL).
- Children negative for all HBV markers received varying doses (5, 10, 20 μg) of HBV vaccine or a combined hepatitis A and B (HAB) vaccine on a 0-1-6 month schedule.
Main Results:
- The 10 μg HBV vaccine group (Group II) demonstrated high seropositive rates (up to 92.8% at 8 years) and sustained geometric mean titers (GMTs).
- Children in Group C (1-<10 mIU/mL) showed robust seropositive rates (up to 98.9%) and high GMTs after revaccination.
- The 10 μg dose with the 0-1-6 month schedule elicited strong, persistent immune responses lasting at least 8 years.
Conclusions:
- A 10 μg hepatitis B vaccine booster with a 0-1-6 month schedule is effective in eliciting robust and durable immune responses in children.
- One-dose revaccination may be suitable for children with pre-existing anti-HBs titers between 1 and <10 mIU/mL.
- These findings support the potential need for and optimal strategy of HBV booster vaccination in children.
Abstract:
Debate continues regarding the need for a booster vaccination in children who received a universal infant hepatitis B virus (HBV) vaccination. The aim was to explore the need and the strategies for the booster HBV vaccination. 8-year prospective cohort study was conducted among children aged 5-15 years in 2009-2010 in Zhejiang Province. The participants were divided into groups A (<0.1 mIU/mL), B (0.1 to < 1 mIU/mL) and C (1 to <10 mIU/mL) according to the pre-booster anti-HBs antibody levels. 5 μg (group I), 10 μg (group II), 20 μg hepatitis B vaccines (group III) or 5 μg hepatitis A and B (HAB) vaccines (group IV) with 0-1-6-month schedule were randomly administered to children negative for all markers. Blood samples were collected at baseline HBV marker testing, 1 month after the first dose, 1 month, 1 year, 5 years and 8 years after the third dose. Among 4170 children, 2326 (55.8%) were negative for all HBV markers. Group II showed the highest seropositive rates of 92.8%, 99.7%, 97.6%, 90.3% and 83.4% with GMTs of 4194.5 mIU/ml, 4163.9 mIU/ml, 466.9 mIU/ml, 190.6 mIU/ml, 122.6 mIU/ml from 1 month after dose 1 to 8 years after dose 3, respectively (P < .01). Participants in group C showed seropositive rates of 98.9%, 99.9%, 99.5%, 95.5%, 92.8% after the revaccination with GMTs of 6519.6 mIU/ml, 5267.4 mIU/ml, 547.1 mIU/ml, 249.5 mIU/ml, 155.3 mIU/ml, respectively, higher than group A and B (P < .001), except 1 month after the third dose. The 10 μg of HBV vaccine with a 0-1-6-month booster regimen may elicit robust responses and persist for 8 years or longer. Additionally, 1-dose revaccination maybe suitable for children with 1 to < 10 mIU/ml anti-HBs titers.
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