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Effects of liver-stage clearance by Primaquine on gametocyte carriage of Plasmodium vivax and P. falciparum.

Identifieur interne : 000D51 ( PubMed/Checkpoint ); précédent : 000D50; suivant : 000D52

Effects of liver-stage clearance by Primaquine on gametocyte carriage of Plasmodium vivax and P. falciparum.

Auteurs : Rahel Wampfler [Suisse] ; Natalie E. Hofmann [Suisse] ; Stephan Karl [Australie] ; Inoni Betuela [Papouasie-Nouvelle-Guinée] ; Benson Kinboro [Papouasie-Nouvelle-Guinée] ; Lina Lorry [Papouasie-Nouvelle-Guinée] ; Mariabeth Silkey [Suisse] ; Leanne J. Robinson [Australie] ; Ivo Mueller [Australie] ; Ingrid Felger [Suisse]

Source :

RBID : pubmed:28732068

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English descriptors

Abstract

Primaquine (PQ) is the only currently licensed antimalarial that prevents Plasmodium vivax (Pv) relapses. It also clears mature P. falciparum (Pf) gametocytes, thereby reducing post-treatment transmission. Randomized PQ treatment in a treatment-to-reinfection cohort in Papua New Guinean children permitted the study of Pv and Pf gametocyte carriage after radical cure and to investigate the contribution of Pv relapses.

DOI: 10.1371/journal.pntd.0005753
PubMed: 28732068


Affiliations:


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<div type="abstract" xml:lang="en">Primaquine (PQ) is the only currently licensed antimalarial that prevents Plasmodium vivax (Pv) relapses. It also clears mature P. falciparum (Pf) gametocytes, thereby reducing post-treatment transmission. Randomized PQ treatment in a treatment-to-reinfection cohort in Papua New Guinean children permitted the study of Pv and Pf gametocyte carriage after radical cure and to investigate the contribution of Pv relapses.</div>
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<Day>21</Day>
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<Month>Jul</Month>
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<ArticleTitle>Effects of liver-stage clearance by Primaquine on gametocyte carriage of Plasmodium vivax and P. falciparum.</ArticleTitle>
<Pagination>
<MedlinePgn>e0005753</MedlinePgn>
</Pagination>
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<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Primaquine (PQ) is the only currently licensed antimalarial that prevents Plasmodium vivax (Pv) relapses. It also clears mature P. falciparum (Pf) gametocytes, thereby reducing post-treatment transmission. Randomized PQ treatment in a treatment-to-reinfection cohort in Papua New Guinean children permitted the study of Pv and Pf gametocyte carriage after radical cure and to investigate the contribution of Pv relapses.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Children received radical cure with Chloroquine, Artemether-Lumefantrine plus either PQ or placebo. Blood samples were subsequently collected in 2-to 4-weekly intervals over 8 months. Gametocytes were detected by quantitative reverse transcription-PCR targeting pvs25 and pfs25.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">PQ treatment reduced the incidence of Pv gametocytes by 73%, which was comparable to the effect of PQ on incidence of blood-stage infections. 92% of Pv and 79% of Pf gametocyte-positive infections were asymptomatic. Pv and to a lesser extent Pf gametocyte positivity and density were associated with high blood-stage parasite densities. Multivariate analysis revealed that the odds of gametocytes were significantly reduced in mixed-species infections compared to single-species infections for both species (ORPv = 0.39 [95% CI 0.25-0.62], ORPf = 0.33 [95% CI 0.18-0.60], p<0.001). No difference between the PQ and placebo treatment arms was observed in density of Pv gametocytes or in the proportion of Pv infections that carried gametocytes. First infections after blood-stage and placebo treatment, likely caused by a relapsing hypnozoite, were equally likely to carry gametocytes than first infections after PQ treatment, likely caused by an infective mosquito bite.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Pv relapses and new infections are associated with similar levels of gametocytaemia. Relapses thus contribute considerably to the Pv reservoir highlighting the importance of effective anti-hypnozoite treatment for efficient control of Pv.</AbstractText>
<AbstractText Label="TRIAL REGISTRATION" NlmCategory="BACKGROUND">ClinicalTrials.gov NCT02143934.</AbstractText>
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<LastName>Wampfler</LastName>
<ForeName>Rahel</ForeName>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>University of Basel, Basel, Switzerland.</Affiliation>
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<LastName>Hofmann</LastName>
<ForeName>Natalie E</ForeName>
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<Affiliation>Swiss Tropical and Public Health Institute, Basel, Switzerland.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>University of Basel, Basel, Switzerland.</Affiliation>
</AffiliationInfo>
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<LastName>Karl</LastName>
<ForeName>Stephan</ForeName>
<Initials>S</Initials>
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<Affiliation>Divison of Population Health and Immunity, The Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Medical Biology, University of Melbourne, Victoria, Australia.</Affiliation>
</AffiliationInfo>
</Author>
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<ForeName>Inoni</ForeName>
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<Affiliation>Vector Borne Diseases Unit, PNG Institute of Medical Research, Goroka, Papua New Guinea.</Affiliation>
</AffiliationInfo>
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<LastName>Kinboro</LastName>
<ForeName>Benson</ForeName>
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<AffiliationInfo>
<Affiliation>Department of Medical Biology, University of Melbourne, Victoria, Australia.</Affiliation>
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