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Comparison of five different vaccination schedules with Haemophilus influenzae type b-tetanus toxoid conjugate

S Kurikka1, H Käyhty, L Saarinen

  • 1National Public Health Institute, Helsinki, Finland.

Insights

Two doses of Haemophilus influenzae type b (Hib) conjugate vaccine (PRP-T) provide adequate infant protection up to 18 months. A three-dose schedule offers superior antibody concentrations compared to two-dose schedules.

Area of Science:

  • Immunology
  • Vaccinology
  • Pediatrics

Background:

  • Haemophilus influenzae type b (Hib) conjugate vaccines are crucial for preventing invasive Hib disease in infants.
  • Optimal vaccination schedules are essential for achieving robust and sustained immune responses.

Purpose of the Study:

  • To compare the immunogenicity of five different vaccination schedules for the Haemophilus influenzae type b (Hib)-tetanus toxoid conjugate (PRP-T) vaccine in infants.
  • To evaluate the duration of antibody persistence following different PRP-T vaccination schedules.

Main Methods:

  • A study involving 196 infants compared four two-dose schedules (1-3, 2-4, 2-6, 4-6 months) and one three-dose schedule (2, 4, 6 months) for the PRP-T vaccine.
  • Vaccines were administered concomitantly with diphtheria-tetanus-pertussis (DTP) and inactivated polio vaccine (IPV).
  • Anti-Hib antibody levels were measured by radioimmunoassay at various time points, including pre-immunization, post-vaccination, and up to 12-24 months of age.

Main Results:

  • All tested PRP-T vaccination schedules demonstrated immunogenicity in infants.
  • Two doses of PRP-T vaccine were sufficient to maintain protective antibody levels (≥0.15 µg/ml) in most children up to 12-18 months.
  • A three-dose schedule elicited significantly higher final antibody concentrations compared to the optimal two-dose schedule.

Conclusions:

  • The PRP-T vaccine is immunogenic when administered with DTP and IPV in schedules starting from 1 to 4 months of age.
  • Two doses of PRP-T vaccine provide adequate protection against Hib disease for at least 12-18 months post-vaccination.
  • While two doses are effective, a three-dose schedule results in higher sustained antibody levels.
Abstract

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