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Antipolyribosyl ribitol phosphate response of premature infants to primary and booster vaccination with a combined diphtheria-tetanus-acellular pertussis-hepatitis B-inactivated polio virus/Haemophilus influenzae type b vaccine.

AbstractBACKGROUND:
Prematurity may be a risk factor for Haemophilus influenzae type b vaccine failure. This article evaluates the Haemophilus influenzae type b immunogenicity of a hexavalent diphtheria-tetanus-acellular pertussis-hepatitis B-inactivated poliovirus/Haemophilus influenzae type b vaccine in preterm infants (< 37 weeks' gestation).
METHODS:
This was an open-label, parallel group study. Preterm (N = 94) and term infants (N = 92) received 3 doses of a diphtheria-tetanus-acellular pertussis-hepatitis B-inactivated poliovirus/Haemophilus influenzae type b vaccine at 2, 4, and 6 months with a booster dose at 18 to 20 months. Antipolyribosyl ribitol phosphate antibody concentrations were determined in serum samples taken before and 1 month after primary and booster vaccination.
RESULTS:
Postprimary seroprotection rates (antipolyribosyl ribitol phosphate > or = 0.15 microg/mL) were lower in preterm than in term infants (92.5% vs 97.8%), with antipolyribosyl ribitol phosphate geometric mean concentrations of 2.241 vs 4.247 microg/mL. A progressive reduction in immune response to the Haemophilus influenzae type b antigen was observed with decreasing length of gestation and decreasing birth weight when cutoff > or = 1 microg/mL was considered. Prebooster seroprotection rates and antipolyribosyl ribitol phosphate geometric mean concentrations were low in both groups (antipolyribosyl ribitol phosphate > or = 1.0 microg/mL in 10.7% of preterm and 28.4% of term infants). A vigorous response to booster vaccination was seen in both groups, with no differences in postbooster seroprotection rates or antipolyribosyl ribitol phosphate geometric mean concentrations between the 2 groups (antipolyribosyl ribitol phosphate > or = 1.0 microg/mL in 100% of preterm and 98.5% of term infants).
CONCLUSIONS:
Primary vaccination with a hexavalent diphtheria-tetanus-acellular pertussis-hepatitis B-inactivated poliovirus/Haemophilus influenzae type b vaccine at 2, 4, and 6 months with a booster dose at 18 to 20 months elicits a satisfactory antipolyribosyl ribitol phosphate response in preterm infants compared with term controls. Immunologic response decreased with decreased gestational age and birth weight.
AuthorsFelix Omeñaca, José Garcia-Sicilia, Pilar García-Corbeira, Reyes Boceta, Victorio Torres
JournalPediatrics (Pediatrics) Vol. 119 Issue 1 Pg. e179-85 (Jan 2007) ISSN: 1098-4275 [Electronic] United States
PMID17145903 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • DTPa-HBV-IPV combined vaccine
  • Diphtheria-Tetanus-Pertussis Vaccine
  • Haemophilus Vaccines
  • Haemophilus influenzae type b polysaccharide vaccine
  • Hepatitis B Vaccines
  • Poliovirus Vaccine, Inactivated
  • Polysaccharides
  • Polysaccharides, Bacterial
  • Vaccines, Combined
  • polyribitol phosphate
Topics
  • Antibody Formation
  • Bacterial Capsules
  • Birth Weight
  • Diphtheria-Tetanus-Pertussis Vaccine
  • Gestational Age
  • Haemophilus Vaccines (immunology)
  • Hepatitis B Vaccines
  • Humans
  • Immunization Schedule
  • Immunization, Secondary
  • Infant
  • Infant, Newborn
  • Infant, Premature (immunology)
  • Poliovirus Vaccine, Inactivated
  • Polysaccharides (immunology)
  • Polysaccharides, Bacterial (immunology)
  • Vaccines, Combined (immunology)

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