ArticleHuman vaccines & immunotherapeutics2025
Age- and time-dependent waning vaccine effectiveness of PPV23 against community-acquired pneumonia among adults aged 60 and older: A cohort study.
Article in Human vaccines & immunotherapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
2 citing papers in PubMed.
- High-throughput antigen discovery using Functional Genomic Vaccinology (FGV) identifies protective Streptococcus pneumoniae vaccine candidates.Nature communications · 2026Article
- Aging and vaccines: impact of immunosenescence and inflammaging in vaccine response.Frontiers in aging · 2026Review
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Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The 23-valent pneumococcal polysaccharide vaccine (PPV23) is recommended for adults to prevent pneumococcal diseases, while its effectiveness over time remains unclear. This study aimed to assess the age- and time-dependent effectiveness of PPV23 in reducing community-acquired pneumonia (CAP) incidence among adults aged 60 and older in China. We conducted a prospective cohort study in Shanghai, China, identifying CAP cases via inpatient and outpatient medical records. Vaccine effectiveness (VE) was estimated using Cox regression models with time-dependent vaccination status, adjusted for demographic characteristics, comorbidities, and seasonal influenza activity. Subgroup analyses stratified by age group, comorbidity status, and observation period were performed. A total of 35,491 participants were included, yielding observation of 158,448 person-years. Overall incidence of CAP was 30.69 (95% confidence interval [CI]: 29.83, 31.57) per 1000 person-years. PPV23 seemed to be ineffective when encompassing all cohort participants in the initial analyses. However, subgroup analyses showed significant adjusted VE for those vaccinated before age 60 (VE = 32.83%, 95% CI: 16.40, 46.03). Significant protection was observed within the first-year post-vaccination (VE = 43.63%, 95% CI: 25.30, 57.47) but declined over time. Furthermore, age-time stratification indicated valid protection for those vaccinated before age 65 within the first year. In addition, VE was higher in those without comorbidities. PPV23 demonstrated modest effectiveness against CAP among those vaccinated before the age of 65 within the first year and decline over time. These findings advocate for prioritizing PPV23 vaccination before age 65 to maximize short-term protection against CAP, underscoring the need for effective booster strategies.
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