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PMID: 21483718 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Effect of pneumococcal conjugate vaccination on serotype-specific carriage and invasive disease in England: a cross-sectional study.

PLoS medicine ·Vol. 8 ·No. 4 ·2011-04-00 ·Pages e1001017

Flasche S, Van Hoek AJ, Sheasby E, Waight P, Andrews N, Sheppard C, George R, Miller E

Abstract

We investigated the effect of the 7-valent pneumococcal conjugate vaccine (PCV7) programme in England on serotype-specific carriage and invasive disease to help understand its role in serotype replacement and predict the impact of higher valency vaccines. Nasopharyngeal swabs were taken from children <5 y old and family members (n=400) 2 y after introduction of PCV7 into routine immunization programs. Proportions carrying Streptococcus pneumoniae and serotype distribution among carried isolates were compared with a similar population prior to PCV7 introduction. Serotype-specific case carrier ratios (CCRs) were estimated using national data on invasive disease. In vaccinated children and their contacts vaccine-type (VT) carriage decreased, but was offset by an increase in non-VT carriage, with no significant overall change in carriage prevalence, odds ratio 1.06 (95% confidence interval 0.76-1.49). The lower CCRs of the replacing serotypes resulted in a net reduction in invasive disease in children. The additional serotypes covered by higher valency vaccines had low carriage but high disease prevalence. Serotype 11C emerged as predominant in carriage but caused no invasive disease whereas 8, 12F, and 22F emerged in disease but had very low carriage prevalence. Because the additional serotypes included in PCV10/13 have high CCRs but low carriage prevalence, vaccinating against them is likely to significantly reduce invasive disease with less risk of serotype replacement. However, a few serotypes with high CCRs could mitigate the benefits of higher valency vaccines. Assessment of the effect of PCV on carriage as well as invasive disease should be part of enhanced surveillance activities for PCVs. Please see later in the article for the Editors' Summary.

MeSH Terms
Adolescent Adult Carrier State/immunology,microbiology Child Child, Preschool Communicable Diseases/epidemiology,immunology,microbiology Cross-Sectional Studies England/epidemiology Female Humans Immunization Programs Male Nasopharynx/immunology,microbiology Odds Ratio Pneumococcal Infections/epidemiology,immunology,microbiology Pneumococcal Vaccines/immunology Prevalence Serotyping Streptococcus pneumoniae/classification,immunology Vaccination/methods Vaccines, Conjugate/immunology,microbiology Young Adult
Chemicals
Pneumococcal Vaccines Vaccines, Conjugate
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Flasche Stefan
Immunisation, Hepatitis and Blood Safety Department, Health Protection Agency, London, United Kingdom.
Van Hoek Albert Jan
Sheasby Elizabeth
Waight Pauline
Andrews Nick
Sheppard Carmen
George Robert
Miller Elizabeth
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Article Info
Journal
PLoS medicine
Abbr.
PLoS Med
ISSN
1549-1676
Published
2011-04-00
Epub
2011-00-05
Pages
e1001017
Language
English
Region
United States
NLM ID
101231360
PMCID
PMC3071372
Subset
IM
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