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Response of Egyptian infants with protein calorie malnutrition to hepatitis B vaccination
Y el-Gamal1, R H Aly, E Hossny
1Pediatric Department of Ain Shams University, Cairo, Egypt.
Insights
Hepatitis B vaccination is effective in infants with protein calorie malnutrition (PCM), achieving high seroprotection rates comparable to healthy infants. This finding supports mass vaccination strategies in developing communities to combat hepatitis B virus infection.
Area of Science:
- Immunology
- Pediatrics
- Public Health
Background:
- Protein calorie malnutrition (PCM) can impair immune responses.
- Hepatitis B virus (HBV) infection poses a significant global health challenge, particularly in developing regions.
- Effective vaccination strategies are crucial for controlling HBV transmission.
Purpose of the Study:
- To evaluate the immunogenicity and seroprotection rates of recombinant hepatitis B vaccine in infants with PCM.
- To compare vaccine response in PCM infants with that of healthy, age- and sex-matched infants.
Main Methods:
- A cohort study involving 31 infants with PCM and 13 healthy controls (2-26 months old).
- Administration of three 10 microgram doses of recombinant hepatitis B vaccine (Engerix-B) at 0, 1, and 6 months.
- Assessment of seroprotection at 8 months post-vaccination.
Main Results:
- High seroprotection rates were observed in both groups at 8 months.
- 87% (27/31) of infants with PCM achieved seroprotection.
- All (13/13) healthy infants achieved seroprotection.
Conclusions:
- Recombinant hepatitis B vaccination is effective in infants with PCM.
- The vaccine demonstrates good immunogenicity in this vulnerable population.
- Hepatitis B vaccination can be safely and effectively implemented for mass vaccination programs in developing communities with high rates of PCM.
Abstract:
The response to recombinant hepatitis B vaccine was assessed in 31 seronegative infants (2-26 months old) with protein calorie malnutrition (PCM), compared with 13 seronegative age- and sex-matched healthy infants. Both groups received three 10 micrograms vaccine doses at 0, 1, and 6 months. At month 8, all healthy infants and 87 per cent (27 out of 31) of PCM infants were seroprotected. Thus, hepatitis B vaccination (Engerix-B, SmithKline Beecham Biologicals) can be used effectively in PCM for mass vaccination in developing communities.
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