The mutual effects on safety and immunogenicity of combined vaccination with 15-valent pneumococcal conjugate vaccine and adsorbed acellular DPT in 3-month healthy infants: A randomized, open-label, controlled, phase III clinical trial.

Hum Vaccin ImmunotherAug 3, 2026 (epub)
Clinical ResearchPediatricsOpen access

Pan Lu-Lu, Mu Hong-Ze, Gao Zhao et al.

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In 30 seconds

This phase III randomized controlled trial assessed the safety and immunogenicity of coadministering the 15-valent pneumococcal conjugate vaccine (PCV15) with the DTaP vaccine in 1110 healthy infants aged 3 months. The results indicated that the seroconversion rates and geometric mean concentrations (GMCs) of DTaP in the coadministration group were non-inferior to those in the DTaP alone group, with a lower incidence of adverse events in the coadministration group.

Key findings

  • Seroconversion rates and GMCs of DTaP in the P+DTP group were non-inferior to the DTaP group.
  • The incidence of adverse events in the P+DTP group was lower than in the P-DTP group.
  • No significant difference in IgG antibody positivity rate between P+DTP and P-DTP groups.

Why it matters

Understanding the safety and immunogenicity of combined vaccinations is crucial for optimizing immunization schedules in infants, potentially improving vaccine uptake and public health outcomes.

Source

Published in Hum Vaccin Immunother. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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