Effectiveness of 10 and 13-valent pneumococcal conjugate vaccines against invasive pneumococcal disease in European children: SpIDnet observational multicentre study
Language English Country Netherlands Media print-electronic
Document type Journal Article, Multicenter Study, Observational Study, Research Support, Non-U.S. Gov't
PubMed
35637067
DOI
10.1016/j.vaccine.2022.05.011
PII: S0264-410X(22)00581-3
Knihovny.cz E-resources
- Keywords
- 10-valent pneumococcal vaccine, 13-valent pneumococcal vaccine, Invasive pneumococcal disease, Pneumococcal Infections, Serotype, Streptococcus pneumoniae,
- MeSH
- Child MeSH
- Infant MeSH
- Humans MeSH
- Immunization Schedule MeSH
- Pneumococcal Infections * epidemiology prevention & control MeSH
- Pneumococcal Vaccines MeSH
- Serogroup MeSH
- Streptococcus pneumoniae * MeSH
- Vaccines, Conjugate MeSH
- Check Tag
- Child MeSH
- Infant MeSH
- Humans MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
- Observational Study MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Pneumococcal Vaccines MeSH
- Vaccines, Conjugate MeSH
BACKGROUND: Pneumococcal conjugate vaccines covering 10 (PCV10) and 13 (PCV13) serotypes have been introduced in the infant immunization schedule of most European countries in 2010-11. To provide additional real-life data, we measured the effectiveness of PCV10 and PCV13 against invasive pneumococcal disease (IPD) in children of 12 European sites (SpIDnet). METHODS: We compared the vaccination status of PCV10 and PCV13 serotype IPD (cases) to that of nonPCV13 serotype IPD (controls) reported in 2012-2018. We calculated pooled effectiveness as (1-vaccination odds ratio)*100, and measured effectiveness over time since booster dose. RESULTS: The PCV13 and PCV10 studies included 2522 IPD cases from ten sites and 486 cases from four sites, respectively. The effectiveness of ≥ 1 PCV13 dose was 84.2% (95 %CI: 79.0-88.1) against PCV13 serotypes (n = 2353) and decreased from 93.1% (87.8-96.1) < 12 months to 85.1% (72.0-92.1) ≥ 24 months after booster dose. PCV13 effectiveness of ≥ 1 dose was 84.7% (55.7-94.7) against fatal PCV13 IPD, 64.5% (43.7-77.6), 83.2% (73.7-89.3) and 85.1% (67.6-93.1) against top serotypes 3, 19A and 1, respectively, and 85.4% (62.3-94.4) against 6C. Serotype 3 and 19A effectiveness declined more rapidly. PCV10 effectiveness of ≥ 1 dose was 84.8% (69.4-92.5) against PCV10 serotypes (n = 370), 27.2% (-187.6 to 81.6) and 85.3% (35.2-96.7) against top serotypes 1 and 7F, 32.5% (-28.3 to 64.5) and -14.4% (-526.5 to 79.1) against vaccine-related serotypes 19A and 6C, respectively. CONCLUSIONS: PCV10 and PCV13 provide similar protection against IPD due to the respective vaccine serotype groups but serotype-specific effectiveness varies by serotype and vaccine. PCV13 provided individual protection against serotype 3 and vaccine-related serotype 6C IPD. PCV10 effectiveness was not significant against vaccine-related serotypes 19A and 6C. PCV13 effectiveness declined with time after booster vaccination. This multinational study enabled measuring serotype-specific vaccine effectiveness with a precision rarely possible at the national level. Such large networks are crucial for the post-licensure evaluation of vaccines.
Epiconcept Paris France; Antwerp university Antwerp Belgium
European Centre for Disease Prevention and Control Stockholm Sweden
General Directorate of Public Health Madrid Spain
Health Agency of Catalunya Barcelona Spain; CIBER Epidemiología y Salud Pública Madrid Spain
Health Protection Surveillance Centre Dublin Ireland
National Institute for Health and Welfare Helsinki Finland
National Institute for Health and Welfare Helsinki Finland; Tampere University Tampere Finland
National Institute for Public Health and the Environment Bilthoven the Netherlands
National Institute of Public Health Prague Czech Republic
Norwegian Institute of Public Health Oslo Norway
Public Health England London United Kingdom
Public Health Scotland Glasgow Scotland UK
Santé publique France the National Public Health Institute Saint Maurice France
Statens Serum Institut Copenhagen Denmark
Temple Street Children's University Hospital Irish Pneumococcal Reference Laboratory Dublin Ireland
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