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Immunity to hepatitis B vaccine in Tanzanian under-5 children
J Metodi1, S Aboud, R Mpembeni
1Department of Paediatrics, Muhimbili University of Health & Allied Sciences, Dar es Salaam, Tanzania.
Insights
Most children under 5 in Tanzania achieved protective hepatitis B immunity with the DPT-hepatitis B vaccine. A birth dose could further enhance hepatitis B immunity in children.
Area of Science:
- Immunology
- Vaccinology
- Public Health
Background:
- Hepatitis B vaccination was implemented in Tanzania in 2002.
- The DPT-hepatitis B vaccine is administered at 4, 8, and 12 weeks of life.
Purpose of the Study:
- To assess hepatitis B virus immunity in children younger than 5 years.
- Evaluate vaccine effectiveness in children attending reproductive and child health (RCH) clinics.
Main Methods:
- A cross-sectional study was conducted in Dar es Salaam, Tanzania.
- Blood samples from 296 children under 5 vaccinated with DPT-HB were analyzed for hepatitis B surface antigen (HB(s)Ag) and antibodies (anti-HB(s), Anti-HB(c)).
- Protective immunity was defined as anti-HB(s) levels ≥10 mIU/ml.
Main Results:
- 69.3% of vaccinated children had protective anti-HB(s) levels.
- Vaccine dose number, time since last dose, and HIV status significantly predicted antibody levels.
- 1.7% of children tested positive for HB(s)Ag, indicating potential vertical transmission.
Conclusions:
- Over two-thirds of children under 5 demonstrated protective immunity against hepatitis B.
- Modifying the immunization schedule to include an early birth dose could bolster hepatitis B immunity.
Background:
Hepatitis B vaccine was introduced in Tanzania in 2002 and is administered as DPT-hepatitis B at 4, 8 and 12 weeks of life.
Aim:
To determine immunity to hepatitis B virus in children under 5 years attending reproductive and child health (RCH) clinics.
Methods:
A cross-sectional, health facility-based study was conducted between July and December 2007 at Temeke, Amana and Mwananyamala municipal hospitals in Dar es Salaam, Tanzania. Children under 5 years who had received DPT-HB vaccine as evidenced by RCH card number 1 were included. Blood samples were collected to determine hepatitis B surface antigen (HB(s)Ag) and antibodies to hepatitis B surface antigen (anti-HB(s)) and hepatitis B core antigen (Anti-HB(c)). An anti-HB(s) level of > or =10 mIU/ml is regarded as protective. Nutritional and HIV status were also determined.
Results:
A total of 296 children under 5 years vaccinated with DPT-HB were recruited, 153 (51.7%) of whom were male. Altogether, 205 (69.3%) children had anti-HB(s) levels > or =10 mIU/ml. The number of DPT-HB vaccine doses, time interval since last DPT-HB dose and HIV status were significant predictors of anti-HB(s) levels. Five children (1.7%) were positive for HB(s)Ag, suggesting possible vertical transmission. No child had anti-HB(c) antibodies.
Conclusion:
More than two-thirds of children under 5 years had protective anti-HB(s) levels. A change in the hepatitis B immunisation schedule to include a dose immediately after birth should improve immunity.
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