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Insufficient immune protection in preterm infants due to delayed or incomplete hexavalent vaccination
Elisabeth Kaiser1, Regine Weber1, Michelle Bous1
1Department of General Pediatrics and Neonatology, Saarland University, Homburg, Germany.
Insights
Vaccination adherence in preterm infants is low, leaving many vulnerable. Improving timely hexavalent vaccinations is crucial for infant immunity and protection against diseases.
Area of Science:
- Neonatal immunology
- Vaccinology
- Pediatric infectious diseases
Background:
- Preterm infants require specific vaccination schedules.
- Hexavalent vaccination is recommended at a 3+1 schedule.
- Assessing immune response in preterm infants is critical.
Purpose of the Study:
- To evaluate vaccination completion and timeliness in preterm infants.
- To analyze antibody responses to hexavalent vaccines in this population.
- To assess the impact of vaccination adherence on infant immunity.
Main Methods:
- ELISA was used to measure plasma antibody concentrations.
- Antibody levels were assessed against poliomyelitis, Hib, diphtheria, and tetanus.
- Paired plasma samples were collected at different time points.
Main Results:
- Transplacental antibodies provided initial protection in most infants.
- Timely vaccination led to complete immune protection at one year.
- Vaccination was incomplete in 73% of infants by one year, with significant antibody deficiencies.
Conclusions:
- 42% of preterm infants had insufficient protection against vaccine-preventable diseases.
- Adherence to the recommended 3+1 vaccination schedule is suboptimal.
- Increased efforts are needed to improve vaccination adherence in preterm infants.
Introduction:
For preterm infants, a 3 + 1 schedule is recommended for hexavalent vaccinations during the first year. The aim of this study was to analyze completion and timeliness of vaccinations in preterm infants of 28 + 0 - 32 + 6 weeks of gestation as part of the PRIMAL study (PRiming of IMmunity At the beginning of Life) and the antibody responses to vaccination antigens.
Methods:
Plasma antibody-concentrations against poliomyelitis, Haemophilus influenzae type b (Hib), diphtheria and tetanus were determined using ELISA and evaluated with respect to their protectiveness.
Results:
Among 82 patients that were recruited, paired plasma samples on admission and at the one year follow up visit were available in 41 infants. In 17 infants, plasma samples were also collected at two months, prior to the first vaccination. Transplacental antibody transfer yielded protective antibody concentrations against the vaccine antigens in 66% (Hib) to 93% (tetanus) of the infants on admission and in 24% (Polio) to 50% (diphtheria) at 2 months. At the one-year follow-up, all infants who received their vaccinations on time had complete immune protection. However, after one year, hexavalent vaccination was incomplete in 30 of 41 infants (73%). Among incompletely vaccinated infants, the proportion lacking protective antibody concentrations ranged from 12% for diphtheria to 27% for polio.
Conclusions:
Due to insufficient adherence to vaccination recommendations, 42% of highly vulnerable preterm neonates were insufficiently protected against one or more vaccine-preventable diseases after one year. Efforts should be increased to improve adherence to the recommended 3 + 1 vaccination schedule in preterm infants.
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