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Updated: May 28, 2026

Assessing Respiratory Immune Responses to Haemophilus Influenzae
Published on: June 29, 2021
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.
Background:
Haemophilus influenzae type b (Hib) vaccine became available for use in Japan in December 2008. The aim of the present study was to evaluate the immunogenicity of Hib vaccine in Japanese preterm infants.
Methods:
Serum samples were obtained from 54 preterm infants before the first vaccination and 1 month after the third. Anti-polyribosylribitol phosphate (PRP) antibodies were measured using an enzyme-linked immunosorbent assay method. Antibody positivity was defined as levels >1 µg/mL.
Results:
Of the 54 preterm infants, 46 (85.2%) achieved antibody levels >1 µg/mL. This compares with the 92.4% reported in full-term infants. The antibody seroconversion rate of infants starting vaccination at 2 months of age was close to being significantly lower than when vaccination was started at 3 months of age (P= 0.060). In addition, the percentage of infants achieving a positive response in the group with a history of antenatal steroid exposure was significantly higher than in those not exposed (P= 0.046). Thus, risk factors for lower Hib antibody concentrations after three doses of vaccine were age at first vaccination and lack of use of antenatal steroids.
Conclusions:
There is a possibility that perinatal factors and the environment unique to preterm infants are related to their lower antibody positivity rates compared to full-term infants. It may therefore be preferable to modify the proposed immunization schedule.
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