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Comparison of immunogenicity of hepatitis B vaccine between low and normal birth weight infants

P Lumbiganon1, P Kowsuwan, P Lumbiganon

  • 1Department of Pediatrics, Faculty of Medicine, Khon Kaen University, Thailand.

Insights

Hepatitis B vaccination shows strong immunogenicity in both low and normal birth weight infants. This study confirms the hepatitis B vaccine (Hevac B Pasteur) is equally effective for all infants, regardless of birth weight.

Area of Science:

  • Immunology
  • Pediatrics
  • Vaccinology

Background:

  • Hepatitis B infection poses a significant global health risk.
  • Infant vaccination is crucial for preventing chronic hepatitis B infection.
  • The immunogenicity of vaccines in low birth weight infants requires careful evaluation.

Purpose of the Study:

  • To compare the immunogenicity of the hepatitis B vaccine (Hevac B Pasteur) in low birth weight infants versus normal birth weight infants.
  • To assess antibody response and seroconversion rates following a standard vaccination schedule.

Main Methods:

  • A comparative study involving 50 low birth weight infants and 50 matched controls (normal birth weight).
  • Hepatitis B vaccine administered at birth, 1, 2, and 12 months.
  • Hepatitis B surface antigen (HBsAg) and anti-HBs antibody levels measured using micro-ELISA at specified time points (birth, 4, 9, and 13 months).

Main Results:

  • Both low birth weight and normal birth weight infants demonstrated comparable immunogenicity.
  • Geometric mean titres of anti-HBs antibodies were similar between the two groups.
  • Seroconversion rates indicated equivalent immune response in both low and normal birth weight infants.

Conclusions:

  • The hepatitis B vaccine (Hevac B Pasteur) is equally immunogenic in low birth weight infants as in normal birth weight infants.
  • The standard vaccination schedule is effective for inducing protective immunity in all infants, irrespective of birth weight.
  • Findings support the routine use of hepatitis B vaccine in low birth weight populations.

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