Immune response to Haemophilus influenzae type b conjugate vaccine in preterm infants

Kennosuke Tsuda1, Shiho Iwasaki, Haruko Horiguchi

  • 1Perinatal Center for Maternity and Neonate Department of Pediatrics, Yokohama City University Medical Center, Yokohama, Kanagawa 232-0024, Japan. tsudaken@bk2.so-net.ne.jp

Insights

Japanese preterm infants showed lower antibody response to the Haemophilus influenzae type b (Hib) vaccine compared to full-term infants. Early vaccination and antenatal steroid exposure were linked to better immunogenicity.

Area of Science:

  • Pediatric Immunology
  • Vaccinology
  • Neonatal Health

Background:

  • The Haemophilus influenzae type b (Hib) vaccine was introduced in Japan in December 2008.
  • Preterm infants represent a unique population with potentially different immune responses.

Purpose of the Study:

  • To assess the immunogenicity of the Hib vaccine in Japanese preterm infants.
  • To identify factors influencing vaccine response in this cohort.

Main Methods:

  • Serum samples collected from 54 preterm infants pre-vaccination and post-third dose.
  • Anti-polyribosylribitol phosphate (PRP) antibody levels measured via ELISA.
  • Antibody positivity defined as >1 µg/mL.

Main Results:

  • 85.2% of preterm infants achieved protective Hib antibody levels (>1 µg/mL), lower than the 92.4% in full-term infants.
  • Vaccination initiated at 2 months showed a trend towards lower seroconversion rates compared to 3 months (P=0.060).
  • Antenatal steroid exposure was associated with significantly higher positive antibody responses (P=0.046).

Conclusions:

  • Preterm infants exhibit lower Hib vaccine immunogenicity compared to full-term infants.
  • Perinatal factors and unique preterm infant environments may influence antibody positivity.
  • Consideration of modifying the immunization schedule for preterm infants may be beneficial.
Abstract

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