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Dominance of vaccine serotypes in pediatric invasive pneumococcal infections in Portugal (2012–2015)

We evaluated the impact of continued 13-valent pneumococcal conjugate vaccine (PCV13) use in the private market (uptake of 61%) in pediatric invasive pneumococcal disease (pIPD) in Portugal (2012–2015). The most frequently detected serotypes were: 3 (n = 32, 13.8%), 14 (n = 23, 9.9%), 1 (n = 23, 9.9...

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Autores principales: Silva-Costa, Catarina, Brito, Maria J., Aguiar, Sandra I., Lopes, Joana P., Ramirez, Mário, Melo-Cristino, José
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327022/
https://www.ncbi.nlm.nih.gov/pubmed/30626918
http://dx.doi.org/10.1038/s41598-018-36799-x
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author Silva-Costa, Catarina
Brito, Maria J.
Aguiar, Sandra I.
Lopes, Joana P.
Ramirez, Mário
Melo-Cristino, José
author_facet Silva-Costa, Catarina
Brito, Maria J.
Aguiar, Sandra I.
Lopes, Joana P.
Ramirez, Mário
Melo-Cristino, José
author_sort Silva-Costa, Catarina
collection PubMed
description We evaluated the impact of continued 13-valent pneumococcal conjugate vaccine (PCV13) use in the private market (uptake of 61%) in pediatric invasive pneumococcal disease (pIPD) in Portugal (2012–2015). The most frequently detected serotypes were: 3 (n = 32, 13.8%), 14 (n = 23, 9.9%), 1 (n = 23, 9.9%), 7F (n = 15, 6.4%), 19A (n = 13, 5.6%), 6B and 15B/C (both n = 12, 5.2%), and 24F, 10A and 12B (all with n = 10, 4.3%). Taken together, non-PCV13 serotypes were responsible for 42.2% of pIPD with a known serotype. The use of PCR to detect and serotype pneumococci in both pleural and cerebrospinal fluid samples contributed to 18.1% (n = 47) of all pIPD. Serotype 3 was mostly detected by PCR (n = 21/32, 65.6%) and resulted from a relevant number of vaccine failures. The incidence of pIPD varied in the different age groups but without a clear trend. There were no obvious declines of the incidence of pIPD due to serotypes included in any of the PCVs, and PCV13 serotypes still accounted for the majority of pIPD (57.8%). Our study indicates that a higher vaccination uptake may be necessary to realize the full benefits of PCVs, even after 15 years of moderate use, and highlights the importance of using molecular methods in pIPD surveillance, since these can lead to substantially increased case ascertainment and identification of particular serotypes as causes of pIPD.
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spelling pubmed-63270222019-01-11 Dominance of vaccine serotypes in pediatric invasive pneumococcal infections in Portugal (2012–2015) Silva-Costa, Catarina Brito, Maria J. Aguiar, Sandra I. Lopes, Joana P. Ramirez, Mário Melo-Cristino, José Sci Rep Article We evaluated the impact of continued 13-valent pneumococcal conjugate vaccine (PCV13) use in the private market (uptake of 61%) in pediatric invasive pneumococcal disease (pIPD) in Portugal (2012–2015). The most frequently detected serotypes were: 3 (n = 32, 13.8%), 14 (n = 23, 9.9%), 1 (n = 23, 9.9%), 7F (n = 15, 6.4%), 19A (n = 13, 5.6%), 6B and 15B/C (both n = 12, 5.2%), and 24F, 10A and 12B (all with n = 10, 4.3%). Taken together, non-PCV13 serotypes were responsible for 42.2% of pIPD with a known serotype. The use of PCR to detect and serotype pneumococci in both pleural and cerebrospinal fluid samples contributed to 18.1% (n = 47) of all pIPD. Serotype 3 was mostly detected by PCR (n = 21/32, 65.6%) and resulted from a relevant number of vaccine failures. The incidence of pIPD varied in the different age groups but without a clear trend. There were no obvious declines of the incidence of pIPD due to serotypes included in any of the PCVs, and PCV13 serotypes still accounted for the majority of pIPD (57.8%). Our study indicates that a higher vaccination uptake may be necessary to realize the full benefits of PCVs, even after 15 years of moderate use, and highlights the importance of using molecular methods in pIPD surveillance, since these can lead to substantially increased case ascertainment and identification of particular serotypes as causes of pIPD. Nature Publishing Group UK 2019-01-09 /pmc/articles/PMC6327022/ /pubmed/30626918 http://dx.doi.org/10.1038/s41598-018-36799-x Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Silva-Costa, Catarina
Brito, Maria J.
Aguiar, Sandra I.
Lopes, Joana P.
Ramirez, Mário
Melo-Cristino, José
Dominance of vaccine serotypes in pediatric invasive pneumococcal infections in Portugal (2012–2015)
title Dominance of vaccine serotypes in pediatric invasive pneumococcal infections in Portugal (2012–2015)
title_full Dominance of vaccine serotypes in pediatric invasive pneumococcal infections in Portugal (2012–2015)
title_fullStr Dominance of vaccine serotypes in pediatric invasive pneumococcal infections in Portugal (2012–2015)
title_full_unstemmed Dominance of vaccine serotypes in pediatric invasive pneumococcal infections in Portugal (2012–2015)
title_short Dominance of vaccine serotypes in pediatric invasive pneumococcal infections in Portugal (2012–2015)
title_sort dominance of vaccine serotypes in pediatric invasive pneumococcal infections in portugal (2012–2015)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327022/
https://www.ncbi.nlm.nih.gov/pubmed/30626918
http://dx.doi.org/10.1038/s41598-018-36799-x
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