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Global impact of 10- and 13-valent pneumococcal conjugate vaccines on pneumococcal meningitis in all ages : The PSERENADE project

Global impact of 10- and 13-valent pneumococcal conjugate vaccines on pneumococcal meningitis in all ages : The PSERENADE project


Title: Global impact of 10- and 13-valent pneumococcal conjugate vaccines on pneumococcal meningitis in all ages : The PSERENADE project
Author: The PSERENADE Team
Date: 2025-03
Language: English
Scope: 4130547
Department: Other departments
Faculty of Medicine
Series: Journal of Infection; 90(3)
ISSN: 0163-4453
DOI: 10.1016/j.jinf.2025.106426
Subject: Incidence; Indirect protection; Pneumococcal conjugate vaccines; Pneumococcal meningitis; Serotype replacement; Serotypes; Vaccine impact; sýklafræði; Microbiology (medical); Infectious Diseases
URI: https://hdl.handle.net/20.500.11815/5436

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Citation:

The PSERENADE Team 2025, 'Global impact of 10- and 13-valent pneumococcal conjugate vaccines on pneumococcal meningitis in all ages : The PSERENADE project', Journal of Infection, vol. 90, no. 3, 106426. https://doi.org/10.1016/j.jinf.2025.106426

Abstract:

Background: Pneumococcal conjugate vaccines (PCVs) introduced in childhood national immunization programs lowered vaccine-type invasive pneumococcal disease (IPD), but replacement with non-vaccine-types persisted throughout the PCV10/13 follow-up period. We assessed PCV10/13 impact on pneumococcal meningitis incidence globally. Methods: The number of cases with serotyped pneumococci detected in cerebrospinal fluid and population denominators were obtained from surveillance sites globally. Site-specific meningitis incidence rate ratios (IRRs) comparing pre-PCV incidence to each year post-PCV10/13 were estimated by age (<5, 5–17 and ≥18 years) using Bayesian multi-level mixed effects Poisson regression, accounting for pre-PCV trends. All-site weighted average IRRs were estimated using linear mixed-effects regression stratified by age, product (PCV10 or PCV13) and prior PCV7 impact (none, moderate, or substantial). Changes in pneumococcal meningitis incidence were estimated overall and for product-specific vaccine-types and non-PCV13-types. Results: Analyses included 10,168 cases <5 y from PCV13 sites and 2849 from PCV10 sites, 3711 and 1549 for 5–17 y and 29,187 and 5653 for ≥18 y from 42 surveillance sites (30 PCV13, 12 PCV10, 2 PCV10/13) in 30 countries, primarily high-income (84%). Six years after PCV10/PCV13 introduction, pneumococcal meningitis declined 48–74% across products and PCV7 impact strata for children <5 y, 35–62% for 5–17 y and 0–36% for ≥18 y. Impact against PCV10-types at PCV10 sites, and PCV13-types at PCV13 sites was high for all age groups (<5 y: 96–100%; 5–17 y: 77–85%; ≥18 y: 73–85%). After switching from PCV7 to PCV10/13, increases in non-PCV13-types were generally low to none for all age groups. Conclusion: Pneumococcal meningitis declined in all age groups following PCV10/PCV13 introduction. Plateaus in non-PCV13-type meningitis suggest less replacement than for all IPD. Data from meningitis belt and high-burden settings were limited.

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