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S. pneumoniae transmission according to inclusion in conjugate vaccines: Bayesian analysis of a longitudinal follow-up in schools

BACKGROUND: Recent trends of pneumococcal colonization in the United States, following the introduction of conjugate vaccination, indicate that non-vaccine serotypes tend to replace vaccine serotypes. The eventual extent of this replacement is however unknown and depends on serotype-specific carriag...

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Autores principales: Cauchemez, Simon, Temime, Laura, Valleron, Alain-Jacques, Varon, Emmanuelle, Thomas, Guy, Guillemot, Didier, Boëlle, Pierre-Yves
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1382230/
https://www.ncbi.nlm.nih.gov/pubmed/16445857
http://dx.doi.org/10.1186/1471-2334-6-14
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author Cauchemez, Simon
Temime, Laura
Valleron, Alain-Jacques
Varon, Emmanuelle
Thomas, Guy
Guillemot, Didier
Boëlle, Pierre-Yves
author_facet Cauchemez, Simon
Temime, Laura
Valleron, Alain-Jacques
Varon, Emmanuelle
Thomas, Guy
Guillemot, Didier
Boëlle, Pierre-Yves
author_sort Cauchemez, Simon
collection PubMed
description BACKGROUND: Recent trends of pneumococcal colonization in the United States, following the introduction of conjugate vaccination, indicate that non-vaccine serotypes tend to replace vaccine serotypes. The eventual extent of this replacement is however unknown and depends on serotype-specific carriage and transmission characteristics. METHODS: Here, some of these characteristics were estimated for vaccine and non-vaccine serotypes from the follow-up of 4,488 schoolchildren in France in 2000. A Bayesian approach using Markov chain Monte Carlo data augmentation techniques was used for estimation. RESULTS: Vaccine and non-vaccine serotypes were found to have similar characteristics: the mean duration of carriage was 23 days (95% credible interval (CI): 21, 25 days) for vaccine serotypes and 22 days (95% CI: 20, 24 days) for non-vaccine serotypes; within a school of size 100, the Secondary Attack Rate was 1.1% (95% CI: 1.0%, 1.2%) for both vaccine and non-vaccine serotypes. CONCLUSION: This study supports that, in 3–6 years old children, no competitive advantage exists for vaccine serotypes compared to non-vaccine serotypes. This is an argument in favour of important serotype replacement. It would be important to validate the result for infants, who are known to be the main reservoir in maintaining transmission. Overall reduction in pathogenicity should also be taken into account in forecasting the future burden of pneumococcal colonization in vaccinated populations.
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spelling pubmed-13822302006-02-28 S. pneumoniae transmission according to inclusion in conjugate vaccines: Bayesian analysis of a longitudinal follow-up in schools Cauchemez, Simon Temime, Laura Valleron, Alain-Jacques Varon, Emmanuelle Thomas, Guy Guillemot, Didier Boëlle, Pierre-Yves BMC Infect Dis Research Article BACKGROUND: Recent trends of pneumococcal colonization in the United States, following the introduction of conjugate vaccination, indicate that non-vaccine serotypes tend to replace vaccine serotypes. The eventual extent of this replacement is however unknown and depends on serotype-specific carriage and transmission characteristics. METHODS: Here, some of these characteristics were estimated for vaccine and non-vaccine serotypes from the follow-up of 4,488 schoolchildren in France in 2000. A Bayesian approach using Markov chain Monte Carlo data augmentation techniques was used for estimation. RESULTS: Vaccine and non-vaccine serotypes were found to have similar characteristics: the mean duration of carriage was 23 days (95% credible interval (CI): 21, 25 days) for vaccine serotypes and 22 days (95% CI: 20, 24 days) for non-vaccine serotypes; within a school of size 100, the Secondary Attack Rate was 1.1% (95% CI: 1.0%, 1.2%) for both vaccine and non-vaccine serotypes. CONCLUSION: This study supports that, in 3–6 years old children, no competitive advantage exists for vaccine serotypes compared to non-vaccine serotypes. This is an argument in favour of important serotype replacement. It would be important to validate the result for infants, who are known to be the main reservoir in maintaining transmission. Overall reduction in pathogenicity should also be taken into account in forecasting the future burden of pneumococcal colonization in vaccinated populations. BioMed Central 2006-01-30 /pmc/articles/PMC1382230/ /pubmed/16445857 http://dx.doi.org/10.1186/1471-2334-6-14 Text en Copyright © 2006 Cauchemez et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Cauchemez, Simon
Temime, Laura
Valleron, Alain-Jacques
Varon, Emmanuelle
Thomas, Guy
Guillemot, Didier
Boëlle, Pierre-Yves
S. pneumoniae transmission according to inclusion in conjugate vaccines: Bayesian analysis of a longitudinal follow-up in schools
title S. pneumoniae transmission according to inclusion in conjugate vaccines: Bayesian analysis of a longitudinal follow-up in schools
title_full S. pneumoniae transmission according to inclusion in conjugate vaccines: Bayesian analysis of a longitudinal follow-up in schools
title_fullStr S. pneumoniae transmission according to inclusion in conjugate vaccines: Bayesian analysis of a longitudinal follow-up in schools
title_full_unstemmed S. pneumoniae transmission according to inclusion in conjugate vaccines: Bayesian analysis of a longitudinal follow-up in schools
title_short S. pneumoniae transmission according to inclusion in conjugate vaccines: Bayesian analysis of a longitudinal follow-up in schools
title_sort s. pneumoniae transmission according to inclusion in conjugate vaccines: bayesian analysis of a longitudinal follow-up in schools
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1382230/
https://www.ncbi.nlm.nih.gov/pubmed/16445857
http://dx.doi.org/10.1186/1471-2334-6-14
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