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Differential Patterns of Infection and Disease with P. falciparum and P. vivax in Young Papua New Guinean Children

BACKGROUND: Where P. vivax and P. falciparum occur in the same population, the peak burden of P. vivax infection and illness is often concentrated in younger age groups. Experiences from malaria therapy patients indicate that immunity is acquired faster to P. vivax than to P. falciparum challenge. T...

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Autores principales: Lin, Enmoore, Kiniboro, Benson, Gray, Laurie, Dobbie, Stuart, Robinson, Leanne, Laumaea, Annemarie, Schöpflin, Sonja, Stanisic, Danielle, Betuela, Inoni, Blood-Zikursh, Melinda, Siba, Peter, Felger, Ingrid, Schofield, Louis, Zimmerman, Peter, Mueller, Ivo
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816213/
https://www.ncbi.nlm.nih.gov/pubmed/20140220
http://dx.doi.org/10.1371/journal.pone.0009047
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author Lin, Enmoore
Kiniboro, Benson
Gray, Laurie
Dobbie, Stuart
Robinson, Leanne
Laumaea, Annemarie
Schöpflin, Sonja
Stanisic, Danielle
Betuela, Inoni
Blood-Zikursh, Melinda
Siba, Peter
Felger, Ingrid
Schofield, Louis
Zimmerman, Peter
Mueller, Ivo
author_facet Lin, Enmoore
Kiniboro, Benson
Gray, Laurie
Dobbie, Stuart
Robinson, Leanne
Laumaea, Annemarie
Schöpflin, Sonja
Stanisic, Danielle
Betuela, Inoni
Blood-Zikursh, Melinda
Siba, Peter
Felger, Ingrid
Schofield, Louis
Zimmerman, Peter
Mueller, Ivo
author_sort Lin, Enmoore
collection PubMed
description BACKGROUND: Where P. vivax and P. falciparum occur in the same population, the peak burden of P. vivax infection and illness is often concentrated in younger age groups. Experiences from malaria therapy patients indicate that immunity is acquired faster to P. vivax than to P. falciparum challenge. There is however little prospective data on the comparative risk of infection and disease from both species in young children living in co-endemic areas. METHODOLOGY/PRINCIPAL FINDINGS: A cohort of 264 Papua New Guinean children aged 1-3 years (at enrolment) were actively followed-up for Plasmodium infection and febrile illness for 16 months. Infection status was determined by light microscopy and PCR every 8 weeks and at each febrile episode. A generalised estimating equation (GEE) approach was used to analyse both prevalence of infection and incidence of clinical episodes. A more pronounced rise in prevalence of P. falciparum compared to P. vivax infection was evident with increasing age. Although the overall incidence of clinical episodes was comparable (P. falciparum: 2.56, P. vivax 2.46 episodes / child / yr), P. falciparum and P. vivax infectious episodes showed strong but opposing age trends: P. falciparum incidence increased until the age of 30 months with little change thereafter, but incidence of P. vivax decreased significantly with age throughout the entire age range. For P. falciparum, both prevalence and incidence of P. falciparum showed marked seasonality, whereas only P. vivax incidence but not prevalence decreased in the dry season. CONCLUSIONS/SIGNIFICANCE: Under high, perennial exposure, children in PNG begin acquiring significant clinical immunity, characterized by an increasing ability to control parasite densities below the pyrogenic threshold to P. vivax, but not to P. falciparum, in the 2(nd) and 3(rd) year of life. The ability to relapse from long-lasting liver-stages restricts the seasonal variation in prevalence of P. vivax infections.
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spelling pubmed-28162132010-02-07 Differential Patterns of Infection and Disease with P. falciparum and P. vivax in Young Papua New Guinean Children Lin, Enmoore Kiniboro, Benson Gray, Laurie Dobbie, Stuart Robinson, Leanne Laumaea, Annemarie Schöpflin, Sonja Stanisic, Danielle Betuela, Inoni Blood-Zikursh, Melinda Siba, Peter Felger, Ingrid Schofield, Louis Zimmerman, Peter Mueller, Ivo PLoS One Research Article BACKGROUND: Where P. vivax and P. falciparum occur in the same population, the peak burden of P. vivax infection and illness is often concentrated in younger age groups. Experiences from malaria therapy patients indicate that immunity is acquired faster to P. vivax than to P. falciparum challenge. There is however little prospective data on the comparative risk of infection and disease from both species in young children living in co-endemic areas. METHODOLOGY/PRINCIPAL FINDINGS: A cohort of 264 Papua New Guinean children aged 1-3 years (at enrolment) were actively followed-up for Plasmodium infection and febrile illness for 16 months. Infection status was determined by light microscopy and PCR every 8 weeks and at each febrile episode. A generalised estimating equation (GEE) approach was used to analyse both prevalence of infection and incidence of clinical episodes. A more pronounced rise in prevalence of P. falciparum compared to P. vivax infection was evident with increasing age. Although the overall incidence of clinical episodes was comparable (P. falciparum: 2.56, P. vivax 2.46 episodes / child / yr), P. falciparum and P. vivax infectious episodes showed strong but opposing age trends: P. falciparum incidence increased until the age of 30 months with little change thereafter, but incidence of P. vivax decreased significantly with age throughout the entire age range. For P. falciparum, both prevalence and incidence of P. falciparum showed marked seasonality, whereas only P. vivax incidence but not prevalence decreased in the dry season. CONCLUSIONS/SIGNIFICANCE: Under high, perennial exposure, children in PNG begin acquiring significant clinical immunity, characterized by an increasing ability to control parasite densities below the pyrogenic threshold to P. vivax, but not to P. falciparum, in the 2(nd) and 3(rd) year of life. The ability to relapse from long-lasting liver-stages restricts the seasonal variation in prevalence of P. vivax infections. Public Library of Science 2010-02-04 /pmc/articles/PMC2816213/ /pubmed/20140220 http://dx.doi.org/10.1371/journal.pone.0009047 Text en Lin et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lin, Enmoore
Kiniboro, Benson
Gray, Laurie
Dobbie, Stuart
Robinson, Leanne
Laumaea, Annemarie
Schöpflin, Sonja
Stanisic, Danielle
Betuela, Inoni
Blood-Zikursh, Melinda
Siba, Peter
Felger, Ingrid
Schofield, Louis
Zimmerman, Peter
Mueller, Ivo
Differential Patterns of Infection and Disease with P. falciparum and P. vivax in Young Papua New Guinean Children
title Differential Patterns of Infection and Disease with P. falciparum and P. vivax in Young Papua New Guinean Children
title_full Differential Patterns of Infection and Disease with P. falciparum and P. vivax in Young Papua New Guinean Children
title_fullStr Differential Patterns of Infection and Disease with P. falciparum and P. vivax in Young Papua New Guinean Children
title_full_unstemmed Differential Patterns of Infection and Disease with P. falciparum and P. vivax in Young Papua New Guinean Children
title_short Differential Patterns of Infection and Disease with P. falciparum and P. vivax in Young Papua New Guinean Children
title_sort differential patterns of infection and disease with p. falciparum and p. vivax in young papua new guinean children
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816213/
https://www.ncbi.nlm.nih.gov/pubmed/20140220
http://dx.doi.org/10.1371/journal.pone.0009047
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