Available evidence on the co-administration of the four-component meningococcal B vaccine (4CMenB) with three vaccines at the same visit among pediatric individuals

Hum Vaccin Immunother. 2024 Dec 31;20(1):2333106. doi: 10.1080/21645515.2024.2333106. Epub 2024 Apr 2.

Abstract

Vaccine co-administration is a useful strategy for improving vaccine coverage and adherence. In Italy, an update to the national immunization program (NIP) in 2023 included recommendations for co-administration of pediatric vaccines, including the four-component vaccine for meningococcus B (4CMenB), pneumococcal conjugate vaccine (PCV), hexavalent vaccines, and oral rotavirus vaccines. Safety is a major concern when considering vaccine co-administration; therefore, a literature review of the available evidence on 4CMenB co-administration with PCV, hexavalent/pentavalent, and rotavirus vaccines was performed. Of 763 publications screened, two studies were reviewed that reported safety data on 4CMenB co-administration with PCV, hexavalent/pentavalent, and rotavirus vaccines in infants aged 0-24 months. Overall, these studies supported that there were no significant safety signals when co-administering 4CMenB with PCV, hexavalent/pentavalent, and rotavirus vaccines, compared with individual vaccination. This review provides key insights for healthcare professionals on the tolerability of co-administering 4CMenB with routine vaccines.

Keywords: 4CMenB; Italy; Neisseria meningitidis; co-administration; national immunization program; vaccination.

Publication types

  • Review

MeSH terms

  • Humans
  • Infant
  • Infant, Newborn
  • Meningococcal Infections* / prevention & control
  • Meningococcal Vaccines* / administration & dosage
  • Neisseria meningitidis, Serogroup B
  • Pneumococcal Vaccines / administration & dosage
  • Rotavirus Vaccines / administration & dosage
  • Vaccination
  • Vaccines, Conjugate / administration & dosage

Substances

  • Meningococcal Vaccines
  • Rotavirus Vaccines
  • Vaccines, Conjugate
  • Pneumococcal Vaccines

Grants and funding

This project was carried out in collaboration with GlaxoSmithKline Biologicals SA. Support for third-party writing assistance for this article was funded by GSK in accordance with Good Publication Practice (GPP 2022) guidelines (https://www.ismpp.org/gpp-2022).