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Hepatitis B virus infection in northern Uganda: Impact of pentavalent hepatitis B vaccination
Eyasu H Teshale1, Saleem Kamili1, Jan Drobeniuc1
1Division of Viral Hepatitis, CDC, Atlanta, United States.
Insights
Uganda
Area of Science:
- Public Health
- Infectious Diseases
- Vaccinology
Background:
- Hepatitis B virus infection (HBV) poses a significant global health burden.
- Vaccination is a primary strategy for preventing chronic hepatitis B virus infection (CHBI).
- Uganda introduced a pentavalent hepatitis B vaccine policy in 2002, with vaccination commencing at 6 weeks of age.
Purpose of the Study:
- To evaluate the effectiveness of the pentavalent hepatitis B vaccine administered at 6 weeks of age in preventing CHBI in Uganda.
- To assess potential infant vulnerability to HBV infection during the first 6 weeks of life under the current vaccination policy.
Main Methods:
- A serologic study was conducted involving 656 individuals tested for HBV.
- Prevalence of chronic HBV infection was determined across different age groups.
- A specific analysis focused on children born after the vaccine policy implementation (aged ≤ 4 years).
Main Results:
- Overall, 9.4% of the 656 individuals tested had chronic HBV infection.
- Among children aged 5-9 years, the prevalence of CHBI was 7.6%.
- Crucially, none of the 73 children born after the vaccine policy's introduction (≤ 4 years old) were infected with HBV (p = 0.003).
Conclusions:
- Vaccination with the pentavalent hepatitis B vaccine at 6 weeks of age was not associated with CHBI in the studied population.
- This vaccination schedule appears effective in preventing HBV infection, including potential mother-to-infant transmission in settings lacking birth-dose vaccination access.
Abstract:
Chronic hepatitis B virus infection (CHBI) is effectively prevented by vaccination starting at birth. Beginning in 2002 Uganda adopted a policy of providing the pentavalent hepatitis B vaccine starting at 6 weeks of age. However, there is concern that this delay may leave the infant vulnerable to infection during the first 6 weeks of life. We assessed whether vaccination at 6 weeks was an effective strategy by HBV serologic study. Of 656 persons tested for HBV, 9.4% were chronically infected; among children aged 5-9 years the prevalence was 7.6%. Of all tested, 73 were born (i.e., aged ≤ 4 years) after the introduction of the pentavalent vaccine; none were infected with HBV (p = 0.003). In this study, vaccination with the pentavalent vaccine at 6 weeks did not result in CHBI, but rather provides an opportunity to prevent mother-to-infant transmission of HBV infection where there is no access to birth-dose vaccine.
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