Cargando…

Determinants of high residual post-PCV13 pneumococcal vaccine-type carriage in Blantyre, Malawi: a modelling study

BACKGROUND: In November 2011, Malawi introduced the 13-valent pneumococcal conjugate vaccine (PCV13) into the routine infant schedule. Four to 7 years after introduction (2015–2018), rolling prospective nasopharyngeal carriage surveys were performed in the city of Blantyre. Carriage of Streptococcus...

Descripción completa

Detalles Bibliográficos
Autores principales: Lourenço, J., Obolski, U., Swarthout, T. D., Gori, A., Bar-Zeev, N., Everett, D., Kamng’ona, A. W., Mwalukomo, T. S., Mataya, A. A., Mwansambo, C., Banda, M., Gupta, S., French, N., Heyderman, R. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894346/
https://www.ncbi.nlm.nih.gov/pubmed/31801542
http://dx.doi.org/10.1186/s12916-019-1450-2
_version_ 1783476375191027712
author Lourenço, J.
Obolski, U.
Swarthout, T. D.
Gori, A.
Bar-Zeev, N.
Everett, D.
Kamng’ona, A. W.
Mwalukomo, T. S.
Mataya, A. A.
Mwansambo, C.
Banda, M.
Gupta, S.
French, N.
Heyderman, R. S.
author_facet Lourenço, J.
Obolski, U.
Swarthout, T. D.
Gori, A.
Bar-Zeev, N.
Everett, D.
Kamng’ona, A. W.
Mwalukomo, T. S.
Mataya, A. A.
Mwansambo, C.
Banda, M.
Gupta, S.
French, N.
Heyderman, R. S.
author_sort Lourenço, J.
collection PubMed
description BACKGROUND: In November 2011, Malawi introduced the 13-valent pneumococcal conjugate vaccine (PCV13) into the routine infant schedule. Four to 7 years after introduction (2015–2018), rolling prospective nasopharyngeal carriage surveys were performed in the city of Blantyre. Carriage of Streptococcus pneumoniae vaccine serotypes (VT) remained higher than reported in high-income countries, and impact was asymmetric across age groups. METHODS: A dynamic transmission model was fit to survey data using a Bayesian Markov-chain Monte Carlo approach, to obtain insights into the determinants of post-PCV13 age-specific VT carriage. RESULTS: Accumulation of naturally acquired immunity with age and age-specific transmission potential were both key to reproducing the observed data. VT carriage reduction peaked sequentially over time, earlier in younger and later in older age groups. Estimated vaccine efficacy (protection against carriage) was 66.87% (95% CI 50.49–82.26%), similar to previous estimates. Ten-year projected vaccine impact (VT carriage reduction) among 0–9 years old was lower than observed in other settings, at 76.23% (CI 95% 68.02–81.96%), with sensitivity analyses demonstrating this to be mainly driven by a high local force of infection. CONCLUSIONS: There are both vaccine-related and host-related determinants of post-PCV13 pneumococcal VT transmission in Blantyre with vaccine impact determined by an age-specific, local force of infection. These findings are likely to be generalisable to other Sub-Saharan African countries in which PCV impact on carriage (and therefore herd protection) has been lower than desired, and have implications for the interpretation of post-PCV carriage studies and future vaccination programs.
format Online
Article
Text
id pubmed-6894346
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-68943462019-12-11 Determinants of high residual post-PCV13 pneumococcal vaccine-type carriage in Blantyre, Malawi: a modelling study Lourenço, J. Obolski, U. Swarthout, T. D. Gori, A. Bar-Zeev, N. Everett, D. Kamng’ona, A. W. Mwalukomo, T. S. Mataya, A. A. Mwansambo, C. Banda, M. Gupta, S. French, N. Heyderman, R. S. BMC Med Research Article BACKGROUND: In November 2011, Malawi introduced the 13-valent pneumococcal conjugate vaccine (PCV13) into the routine infant schedule. Four to 7 years after introduction (2015–2018), rolling prospective nasopharyngeal carriage surveys were performed in the city of Blantyre. Carriage of Streptococcus pneumoniae vaccine serotypes (VT) remained higher than reported in high-income countries, and impact was asymmetric across age groups. METHODS: A dynamic transmission model was fit to survey data using a Bayesian Markov-chain Monte Carlo approach, to obtain insights into the determinants of post-PCV13 age-specific VT carriage. RESULTS: Accumulation of naturally acquired immunity with age and age-specific transmission potential were both key to reproducing the observed data. VT carriage reduction peaked sequentially over time, earlier in younger and later in older age groups. Estimated vaccine efficacy (protection against carriage) was 66.87% (95% CI 50.49–82.26%), similar to previous estimates. Ten-year projected vaccine impact (VT carriage reduction) among 0–9 years old was lower than observed in other settings, at 76.23% (CI 95% 68.02–81.96%), with sensitivity analyses demonstrating this to be mainly driven by a high local force of infection. CONCLUSIONS: There are both vaccine-related and host-related determinants of post-PCV13 pneumococcal VT transmission in Blantyre with vaccine impact determined by an age-specific, local force of infection. These findings are likely to be generalisable to other Sub-Saharan African countries in which PCV impact on carriage (and therefore herd protection) has been lower than desired, and have implications for the interpretation of post-PCV carriage studies and future vaccination programs. BioMed Central 2019-12-05 /pmc/articles/PMC6894346/ /pubmed/31801542 http://dx.doi.org/10.1186/s12916-019-1450-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Lourenço, J.
Obolski, U.
Swarthout, T. D.
Gori, A.
Bar-Zeev, N.
Everett, D.
Kamng’ona, A. W.
Mwalukomo, T. S.
Mataya, A. A.
Mwansambo, C.
Banda, M.
Gupta, S.
French, N.
Heyderman, R. S.
Determinants of high residual post-PCV13 pneumococcal vaccine-type carriage in Blantyre, Malawi: a modelling study
title Determinants of high residual post-PCV13 pneumococcal vaccine-type carriage in Blantyre, Malawi: a modelling study
title_full Determinants of high residual post-PCV13 pneumococcal vaccine-type carriage in Blantyre, Malawi: a modelling study
title_fullStr Determinants of high residual post-PCV13 pneumococcal vaccine-type carriage in Blantyre, Malawi: a modelling study
title_full_unstemmed Determinants of high residual post-PCV13 pneumococcal vaccine-type carriage in Blantyre, Malawi: a modelling study
title_short Determinants of high residual post-PCV13 pneumococcal vaccine-type carriage in Blantyre, Malawi: a modelling study
title_sort determinants of high residual post-pcv13 pneumococcal vaccine-type carriage in blantyre, malawi: a modelling study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894346/
https://www.ncbi.nlm.nih.gov/pubmed/31801542
http://dx.doi.org/10.1186/s12916-019-1450-2
work_keys_str_mv AT lourencoj determinantsofhighresidualpostpcv13pneumococcalvaccinetypecarriageinblantyremalawiamodellingstudy
AT obolskiu determinantsofhighresidualpostpcv13pneumococcalvaccinetypecarriageinblantyremalawiamodellingstudy
AT swarthouttd determinantsofhighresidualpostpcv13pneumococcalvaccinetypecarriageinblantyremalawiamodellingstudy
AT goria determinantsofhighresidualpostpcv13pneumococcalvaccinetypecarriageinblantyremalawiamodellingstudy
AT barzeevn determinantsofhighresidualpostpcv13pneumococcalvaccinetypecarriageinblantyremalawiamodellingstudy
AT everettd determinantsofhighresidualpostpcv13pneumococcalvaccinetypecarriageinblantyremalawiamodellingstudy
AT kamngonaaw determinantsofhighresidualpostpcv13pneumococcalvaccinetypecarriageinblantyremalawiamodellingstudy
AT mwalukomots determinantsofhighresidualpostpcv13pneumococcalvaccinetypecarriageinblantyremalawiamodellingstudy
AT matayaaa determinantsofhighresidualpostpcv13pneumococcalvaccinetypecarriageinblantyremalawiamodellingstudy
AT mwansamboc determinantsofhighresidualpostpcv13pneumococcalvaccinetypecarriageinblantyremalawiamodellingstudy
AT bandam determinantsofhighresidualpostpcv13pneumococcalvaccinetypecarriageinblantyremalawiamodellingstudy
AT guptas determinantsofhighresidualpostpcv13pneumococcalvaccinetypecarriageinblantyremalawiamodellingstudy
AT frenchn determinantsofhighresidualpostpcv13pneumococcalvaccinetypecarriageinblantyremalawiamodellingstudy
AT heydermanrs determinantsofhighresidualpostpcv13pneumococcalvaccinetypecarriageinblantyremalawiamodellingstudy