A comparative study of PENTA vaccine booster doses given at 12, 15, or 18 months of age

D W Scheifele1, R Guasparini, P Lavigne

  • 1Vaccine Evaluation Center, BC's Children's Hospital, Vancouver, Canada.

Vaccine
|March 13, 1999
PubMed

Insights

Booster immunization with Haemophilus influenzae type b conjugate vaccines (PRP-T) between 12 and 18 months shows stable antibody levels. While 12-month boosters have milder side effects, 18-month boosters elicit stronger immune responses to most antigens.

Area of Science:

  • Pediatric immunology
  • Vaccinology
  • Infectious disease prevention

Background:

  • Booster doses of Haemophilus influenzae type b conjugate vaccines are typically given between 12-18 months.
  • The optimal timing for these boosters to maximize immune response and minimize adverse effects is not fully established.

Purpose of the Study:

  • To evaluate the impact of booster immunization timing (12, 15, or 18 months) on pre-immunization antibody levels and subsequent immune responses to a PRP-T conjugate vaccine.
  • To assess local injection site reactions associated with different booster timings.

Main Methods:

  • A randomized controlled trial involving 253 healthy children previously immunized with a PENTA vaccine (DPT-IPV/PRP-T).
  • Children received their PENTA booster concurrently with MMR vaccine at 12, 15, or 18 months.
  • Antibody levels (anti-PRP and others) and adverse events were measured before and 4 weeks after booster vaccination.

Main Results:

  • Pre-booster anti-PRP antibody levels were comparable across all age groups.
  • Post-booster anti-PRP geometric mean concentrations (GMCs) were significantly higher in older children (18 months) compared to younger ones (12 months).
  • Booster responses to other vaccine antigens were strongest when administered at 18 months; however, 12-month boosters showed less injection site morbidity.

Conclusions:

  • Anti-PRP antibody levels remain stable in children aged 12-18 months who have previously received PRP-T vaccination.
  • While 18-month boosters yield superior immune responses to most antigens, 12-month boosters are associated with reduced local reactions.
  • All tested ages demonstrated satisfactory immune responses, suggesting flexibility in booster timing within this window.

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