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Population heterogeneity in Plasmodium vivax relapse risk

A key characteristic of Plasmodium vivax parasites is their ability to adopt a latent liver-stage form called hypnozoites, able to cause relapse of infection months or years after a primary infection. Relapses of infection through hypnozoite activation are a major contributor to blood-stage infectio...

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Autores principales: Stadler, Eva, Cromer, Deborah, Mehra, Somya, Adekunle, Adeshina I., Flegg, Jennifer A., Anstey, Nicholas M., Watson, James A., Chu, Cindy S., Mueller, Ivo, Robinson, Leanne J., Schlub, Timothy E., Davenport, Miles P., Khoury, David S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9810152/
https://www.ncbi.nlm.nih.gov/pubmed/36534705
http://dx.doi.org/10.1371/journal.pntd.0010990
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author Stadler, Eva
Cromer, Deborah
Mehra, Somya
Adekunle, Adeshina I.
Flegg, Jennifer A.
Anstey, Nicholas M.
Watson, James A.
Chu, Cindy S.
Mueller, Ivo
Robinson, Leanne J.
Schlub, Timothy E.
Davenport, Miles P.
Khoury, David S.
author_facet Stadler, Eva
Cromer, Deborah
Mehra, Somya
Adekunle, Adeshina I.
Flegg, Jennifer A.
Anstey, Nicholas M.
Watson, James A.
Chu, Cindy S.
Mueller, Ivo
Robinson, Leanne J.
Schlub, Timothy E.
Davenport, Miles P.
Khoury, David S.
author_sort Stadler, Eva
collection PubMed
description A key characteristic of Plasmodium vivax parasites is their ability to adopt a latent liver-stage form called hypnozoites, able to cause relapse of infection months or years after a primary infection. Relapses of infection through hypnozoite activation are a major contributor to blood-stage infections in P vivax endemic regions and are thought to be influenced by factors such as febrile infections which may cause temporary changes in hypnozoite activation leading to ‘temporal heterogeneity’ in reactivation risk. In addition, immunity and variation in exposure to infection may be longer-term characteristics of individuals that lead to ‘population heterogeneity’ in hypnozoite activation. We analyze data on risk of P vivax in two previously published data sets from Papua New Guinea and the Thailand-Myanmar border region. Modeling different mechanisms of reactivation risk, we find strong evidence for population heterogeneity, with 30% of patients having almost 70% of all P vivax infections. Model fitting and data analysis indicates that individual variation in relapse risk is a primary source of heterogeneity of P vivax risk of recurrences. Trial Registration: ClinicalTrials.gov NCT01640574, NCT01074905, NCT02143934.
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spelling pubmed-98101522023-01-04 Population heterogeneity in Plasmodium vivax relapse risk Stadler, Eva Cromer, Deborah Mehra, Somya Adekunle, Adeshina I. Flegg, Jennifer A. Anstey, Nicholas M. Watson, James A. Chu, Cindy S. Mueller, Ivo Robinson, Leanne J. Schlub, Timothy E. Davenport, Miles P. Khoury, David S. PLoS Negl Trop Dis Research Article A key characteristic of Plasmodium vivax parasites is their ability to adopt a latent liver-stage form called hypnozoites, able to cause relapse of infection months or years after a primary infection. Relapses of infection through hypnozoite activation are a major contributor to blood-stage infections in P vivax endemic regions and are thought to be influenced by factors such as febrile infections which may cause temporary changes in hypnozoite activation leading to ‘temporal heterogeneity’ in reactivation risk. In addition, immunity and variation in exposure to infection may be longer-term characteristics of individuals that lead to ‘population heterogeneity’ in hypnozoite activation. We analyze data on risk of P vivax in two previously published data sets from Papua New Guinea and the Thailand-Myanmar border region. Modeling different mechanisms of reactivation risk, we find strong evidence for population heterogeneity, with 30% of patients having almost 70% of all P vivax infections. Model fitting and data analysis indicates that individual variation in relapse risk is a primary source of heterogeneity of P vivax risk of recurrences. Trial Registration: ClinicalTrials.gov NCT01640574, NCT01074905, NCT02143934. Public Library of Science 2022-12-19 /pmc/articles/PMC9810152/ /pubmed/36534705 http://dx.doi.org/10.1371/journal.pntd.0010990 Text en © 2022 Stadler et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Stadler, Eva
Cromer, Deborah
Mehra, Somya
Adekunle, Adeshina I.
Flegg, Jennifer A.
Anstey, Nicholas M.
Watson, James A.
Chu, Cindy S.
Mueller, Ivo
Robinson, Leanne J.
Schlub, Timothy E.
Davenport, Miles P.
Khoury, David S.
Population heterogeneity in Plasmodium vivax relapse risk
title Population heterogeneity in Plasmodium vivax relapse risk
title_full Population heterogeneity in Plasmodium vivax relapse risk
title_fullStr Population heterogeneity in Plasmodium vivax relapse risk
title_full_unstemmed Population heterogeneity in Plasmodium vivax relapse risk
title_short Population heterogeneity in Plasmodium vivax relapse risk
title_sort population heterogeneity in plasmodium vivax relapse risk
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9810152/
https://www.ncbi.nlm.nih.gov/pubmed/36534705
http://dx.doi.org/10.1371/journal.pntd.0010990
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