Immunogenicity for 16 serotypes of a unique schedule of pneumococcal vaccines in a high-risk population

Amanda J Leach1, Peter S Morris, Grant Mackenzie

  • 1Menzies School of Health Research, Charles Darwin University, Darwin, Australia. amanda@menzies.edu.au

Vaccine
|June 20, 2008
PubMed

Insights

The 7-valent pneumococcal conjugate vaccine (7PCV) and 23-valent pneumococcal polysaccharide vaccine (23PPV) showed strong immunogenicity in Australian Aboriginal infants. This study evaluated antibody concentrations following vaccination schedules.

Area of Science:

  • Immunology
  • Vaccinology
  • Pediatrics

Background:

  • A specialized vaccination schedule using 7-valent pneumococcal conjugate vaccine (7PCV) and 23-valent pneumococcal polysaccharide vaccine (23PPV) was implemented for Australian Aboriginal infants in 2001.
  • This schedule involved 7PCV at 2, 4, and 6 months, followed by 23PPV at 18 months.

Purpose of the Study:

  • To assess the immunogenicity of the 7PCV and 23PPV vaccination schedule in Australian Aboriginal infants.
  • To determine anti-capsular IgG concentrations in vaccinated infants compared to a historic control group.

Main Methods:

  • Anti-capsular IgG concentrations were measured using a blinded, (22F absorbed) ELISA.
  • Vaccinated infants were compared against non-vaccinated historic control infants.
  • Measurements were taken one month after the third dose of 7PCV and one month after the 23PPV dose.

Main Results:

  • Following three doses of 7PCV, geometric mean concentrations (GMCs) exceeded 1.95 microg/ml, with over 89% of infants achieving IgG levels >0.35 microg/ml for all 7 serotypes.
  • One month post-23PPV, more than 96% of infants had IgG >0.35 microg/ml to 7PCV serotypes, and over 50% had IgG >0.35 microg/ml to non-7PCV serotypes (including 6A, but not 12F or 19A).
  • High IgG levels were sustained for the 7PCV serotypes after the 23PPV booster.

Conclusions:

  • The 7-valent pneumococcal conjugate vaccine (7PCV) and 23-valent pneumococcal polysaccharide vaccine (23PPV) demonstrate significant immunogenicity in Australian Aboriginal infants.
  • The implemented vaccination schedule effectively elicits protective antibody responses against key pneumococcal serotypes in this population.
Abstract

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