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Published on: August 7, 2017
Adverse events and antibody response to accelerated immunisation in term and preterm infants
M E Ramsay1, E Miller, L A Ashworth
1Immunisation Division, PHLS Communicable Disease Surveillance Centre, London.
Insights
Preterm infants demonstrate safe and effective antibody responses to diphtheria, tetanus, and pertussis vaccines administered on the standard schedule. This study confirms that vaccination at chronological age is appropriate for all infants, regardless of gestational age.
Area of Science:
- Pediatrics
- Immunology
- Vaccinology
Background:
- Preterm infants may have different responses to vaccines compared to full-term infants.
- The current national schedule recommends vaccination at chronological age for all infants.
Purpose of the Study:
- To compare adverse events and antibody responses in term and preterm infants receiving the diphtheria, tetanus, and pertussis (DTaP) vaccine.
- To evaluate the safety and immunogenicity of the DTaP vaccine in infants based on gestational age.
Main Methods:
- A cohort of 124 infants was divided into three groups based on gestational age: <34 weeks, 34-36 weeks, and ≥37 weeks.
- Infants received DTaP vaccinations at 2, 3, and 4 months of chronological age.
- Adverse events were monitored 24 hours post-vaccination; antibody titers were measured six weeks after the final dose.
Main Results:
- No significant differences in adverse events were observed between the gestational age groups.
- All infants achieved protective antibody levels for diphtheria and tetanus.
- Antibody titers to pertussis components varied, with some higher in preterm groups, but all demonstrated robust immune responses.
Conclusions:
- The DTaP vaccine is safe and elicits adequate antibody responses in preterm infants when administered according to the standard chronological age schedule.
- These findings support the current practice of vaccinating preterm infants concurrently with their full-term peers.
Abstract:
A study was performed to compare adverse events and antibody response in term and preterm children vaccinated with diphtheria, tetanus, and pertussis vaccine at 2, 3, and 4 months of age. A total of 124 children were recruited and grouped according to gestational age: 37 weeks or more (n = 52), 34 to 36 weeks (n = 40), and less than 34 weeks (n = 32). Study nurses followed up children 24 hours after each vaccination to record temperature, redness, and swelling at the injection site and any systemic symptoms. Proportions of children experiencing adverse events did not differ between groups. Blood samples were obtained six weeks after the vaccination course at which time all children had protective levels of diphtheria and tetanus antitoxins. Geometric mean antibody titres (95% confidence interval) to pertussis toxin were 2754 (2042 to 3715), 5495 (4074 to 7413), and 3690 (2951 to 4677), to filamentous haemagglutinin were 541 (282 to 1023), 951 (537 to 1698), and 614 (426 to 1023), and to agglutinogens 2 and 3 were 12,106 (6918 to 21,380), 21,330 (13,183 to 34,674), and 22,387 (15,136 to 33,113) in children born at a gestational age of less than 34 weeks, 34 to 36 weeks, and 37 weeks or more respectively. These findings support the current recommendations that preterm children are vaccinated at chronological age according to the national schedule.
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