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Did Large-Scale Vaccination Drive Changes in the Circulating Rotavirus Population in Belgium?

Vaccination can place selective pressures on viral populations, leading to changes in the distribution of strains as viruses evolve to escape immunity from the vaccine. Vaccine-driven strain replacement is a major concern after nationwide rotavirus vaccine introductions. However, the distribution of...

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Autores principales: Pitzer, Virginia E., Bilcke, Joke, Heylen, Elisabeth, Crawford, Forrest W., Callens, Michael, De Smet, Frank, Van Ranst, Marc, Zeller, Mark, Matthijnssens, Jelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4685644/
https://www.ncbi.nlm.nih.gov/pubmed/26687288
http://dx.doi.org/10.1038/srep18585
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author Pitzer, Virginia E.
Bilcke, Joke
Heylen, Elisabeth
Crawford, Forrest W.
Callens, Michael
De Smet, Frank
Van Ranst, Marc
Zeller, Mark
Matthijnssens, Jelle
author_facet Pitzer, Virginia E.
Bilcke, Joke
Heylen, Elisabeth
Crawford, Forrest W.
Callens, Michael
De Smet, Frank
Van Ranst, Marc
Zeller, Mark
Matthijnssens, Jelle
author_sort Pitzer, Virginia E.
collection PubMed
description Vaccination can place selective pressures on viral populations, leading to changes in the distribution of strains as viruses evolve to escape immunity from the vaccine. Vaccine-driven strain replacement is a major concern after nationwide rotavirus vaccine introductions. However, the distribution of the predominant rotavirus genotypes varies from year to year in the absence of vaccination, making it difficult to determine what changes can be attributed to the vaccines. To gain insight in the underlying dynamics driving changes in the rotavirus population, we fitted a hierarchy of mathematical models to national and local genotype-specific hospitalization data from Belgium, where large-scale vaccination was introduced in 2006. We estimated that natural- and vaccine-derived immunity was strongest against completely homotypic strains and weakest against fully heterotypic strains, with an intermediate immunity amongst partially heterotypic strains. The predominance of G2P[4] infections in Belgium after vaccine introduction can be explained by a combination of natural genotype fluctuations and weaker natural and vaccine-induced immunity against infection with strains heterotypic to the vaccine, in the absence of significant variation in strain-specific vaccine effectiveness against disease. However, the incidence of rotavirus gastroenteritis is predicted to remain low despite vaccine-driven changes in the distribution of genotypes.
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spelling pubmed-46856442015-12-30 Did Large-Scale Vaccination Drive Changes in the Circulating Rotavirus Population in Belgium? Pitzer, Virginia E. Bilcke, Joke Heylen, Elisabeth Crawford, Forrest W. Callens, Michael De Smet, Frank Van Ranst, Marc Zeller, Mark Matthijnssens, Jelle Sci Rep Article Vaccination can place selective pressures on viral populations, leading to changes in the distribution of strains as viruses evolve to escape immunity from the vaccine. Vaccine-driven strain replacement is a major concern after nationwide rotavirus vaccine introductions. However, the distribution of the predominant rotavirus genotypes varies from year to year in the absence of vaccination, making it difficult to determine what changes can be attributed to the vaccines. To gain insight in the underlying dynamics driving changes in the rotavirus population, we fitted a hierarchy of mathematical models to national and local genotype-specific hospitalization data from Belgium, where large-scale vaccination was introduced in 2006. We estimated that natural- and vaccine-derived immunity was strongest against completely homotypic strains and weakest against fully heterotypic strains, with an intermediate immunity amongst partially heterotypic strains. The predominance of G2P[4] infections in Belgium after vaccine introduction can be explained by a combination of natural genotype fluctuations and weaker natural and vaccine-induced immunity against infection with strains heterotypic to the vaccine, in the absence of significant variation in strain-specific vaccine effectiveness against disease. However, the incidence of rotavirus gastroenteritis is predicted to remain low despite vaccine-driven changes in the distribution of genotypes. Nature Publishing Group 2015-12-21 /pmc/articles/PMC4685644/ /pubmed/26687288 http://dx.doi.org/10.1038/srep18585 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Pitzer, Virginia E.
Bilcke, Joke
Heylen, Elisabeth
Crawford, Forrest W.
Callens, Michael
De Smet, Frank
Van Ranst, Marc
Zeller, Mark
Matthijnssens, Jelle
Did Large-Scale Vaccination Drive Changes in the Circulating Rotavirus Population in Belgium?
title Did Large-Scale Vaccination Drive Changes in the Circulating Rotavirus Population in Belgium?
title_full Did Large-Scale Vaccination Drive Changes in the Circulating Rotavirus Population in Belgium?
title_fullStr Did Large-Scale Vaccination Drive Changes in the Circulating Rotavirus Population in Belgium?
title_full_unstemmed Did Large-Scale Vaccination Drive Changes in the Circulating Rotavirus Population in Belgium?
title_short Did Large-Scale Vaccination Drive Changes in the Circulating Rotavirus Population in Belgium?
title_sort did large-scale vaccination drive changes in the circulating rotavirus population in belgium?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4685644/
https://www.ncbi.nlm.nih.gov/pubmed/26687288
http://dx.doi.org/10.1038/srep18585
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