Association of Routine Infant Vaccinations With Antibody Levels Among Preterm Infants

Elsbeth D M Rouers1,2, Patricia C J Bruijning-Verhagen1,2, Pieter G M van Gageldonk1

  • 1Centre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), Bilthoven, the Netherlands.

JAMA
|September 15, 2020
PubMed

Insights

Routine infant vaccinations may not fully protect preterm infants, though most achieve protective antibody levels after boosters. Antibody concentrations were generally lower in preterm infants compared to term infants, highlighting potential immunization gaps.

Area of Science:

  • Pediatrics
  • Immunology
  • Neonatology

Background:

  • Standard infant immunization schedules may be insufficient for extremely and very preterm infants.
  • Preterm infants represent a vulnerable population requiring specific attention to vaccine efficacy.

Purpose of the Study:

  • To evaluate the immunogenicity of routine vaccinations in preterm infants.
  • To compare antibody responses in preterm infants to those of healthy term infants.

Main Methods:

  • A multicenter, prospective, observational cohort study involving 296 preterm infants and 66 term infants.
  • Infants received routine combination vaccines (diphtheria, tetanus, pertussis, polio, Hib, Hep B) and pneumococcal conjugate vaccine.
  • Antibody levels (IgG) were measured after primary series and booster doses.

Main Results:

  • After the primary series, protective IgG levels varied, with lower responses for Haemophilus influenzae type b (Hib) and certain pneumococcal serotypes.
  • Following the booster dose, over 95% achieved protective levels, except for Hib (88.1%).
  • Geometric mean concentrations of antibodies were generally lower in preterm infants compared to term infants, with exceptions for pertussis and specific pneumococcal serotypes.

Conclusions:

  • Routine vaccinations provide protective antibody levels against most antigens in preterm infants after a booster dose, with Hib as a notable exception.
  • Lower antibody concentrations in preterm infants compared to term infants suggest potential challenges in achieving long-term immunity.
  • Further research may be needed to optimize vaccination strategies for preterm infants to ensure adequate protection.
Abstract

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