Cargando…
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...
Autores principales: | , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1784863249898930176 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9810152 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT stadlereva populationheterogeneityinplasmodiumvivaxrelapserisk AT cromerdeborah populationheterogeneityinplasmodiumvivaxrelapserisk AT mehrasomya populationheterogeneityinplasmodiumvivaxrelapserisk AT adekunleadeshinai populationheterogeneityinplasmodiumvivaxrelapserisk AT fleggjennifera populationheterogeneityinplasmodiumvivaxrelapserisk AT ansteynicholasm populationheterogeneityinplasmodiumvivaxrelapserisk AT watsonjamesa populationheterogeneityinplasmodiumvivaxrelapserisk AT chucindys populationheterogeneityinplasmodiumvivaxrelapserisk AT muellerivo populationheterogeneityinplasmodiumvivaxrelapserisk AT robinsonleannej populationheterogeneityinplasmodiumvivaxrelapserisk AT schlubtimothye populationheterogeneityinplasmodiumvivaxrelapserisk AT davenportmilesp populationheterogeneityinplasmodiumvivaxrelapserisk AT khourydavids populationheterogeneityinplasmodiumvivaxrelapserisk |