Evidence map›Paper›PMID 29389671›Full record

Trial reportThe Journal of clinical investigation2018

A controlled human malaria infection model enabling evaluation of transmission-blocking interventions.

Katharine A Collins, Claire Yt Wang, Matthew Adams, Hayley Mitchell, Melanie Rampton, Suzanne Elliott, Isaie J Reuling, Teun Bousema, Robert Sauerwein, Stephan Chalon and 2 more

2 registry-linked trialsOpen access · hybridAbstract readClinical Trial, Phase IComparative StudyMulticenter Study
In one paragraph

Trial report in The Journal of clinical investigation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 73 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 1 pooled it
21.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02431637 phase1completednot on this map

Blood Stage Challenge Study to Asses Mosquito Transmissibility in Participants Inoculated With Plasmodium Falciparum

TypeinterventionalSponsorMedicines for Malaria VentureRan2015 to 2016Enrolled6ConditionsMalariaArmsAdministration of the malaria inoculum, Piperaquine Phosphate 480 mg
NCT02431650 phase1 / phase2completednot on this map

A Proof-Of-Concept Study to Assess the Effectiveness of OZ439 as a Gametocytocidal and Transmission Blocking Agent in Experimental P. Falciparum Infection

TypeinterventionalSponsorMedicines for Malaria VentureRan2015 to 2016Enrolled11ConditionsMalariaArmsOZ439, Primaquine
3 · Its place in the literature

Who cites it

73 citing papers in PubMed, 1 synthesis or guideline pooled it, 147 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Article
  7. Article
  8. A single-cell atlas ofbioRxiv : the preprint server for biology · 2026
    Article
  9. Article
  10. Towards an evolutionary baseline model ofbioRxiv : the preprint server for biology · 2025
    Article
  11. Evaluation ofiScience · 2025
    Article
  12. Article
  13. Article
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  15. Article
  16. Article
  17. Review
  18. Investigating the dynamics ofOpen research Europe · 2025
    Article
  19. Review
  20. Malaria vaccines: a new era of prevention and control.Nature reviews. Microbiology · 2024
    Review

13 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 3 countries.

Katharine A CollinsQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Claire Yt WangQueensland Paediatric Infectious Diseases (QPID) Laboratory, Centre for Children's Health Research, Brisbane, Queensland, Australia.
Matthew AdamsQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Hayley MitchellQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Melanie RamptonQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Suzanne ElliottQ-Pharm Pty. Ltd., Brisbane, Queensland, Australia.
Isaie J ReulingRadboud Institute for Health Science, Radboud University Medical Center, Nijmegen, Netherlands.
Teun BousemaRadboud Institute for Health Science, Radboud University Medical Center, Nijmegen, Netherlands.
Robert SauerweinRadboud Institute for Health Science, Radboud University Medical Center, Nijmegen, Netherlands.
Stephan ChalonMedicines for Malaria Venture, Geneva, Switzerland.
Jörg J MöhrleMedicines for Malaria Venture, Geneva, Switzerland.
James S McCarthyQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
QIMR Berghofer Medical Research Institute · AURadboud University Nijmegen · NLMedicines for Malaria Venture · CHQ-Pharm · AUQueensland Health · AU

Funding

European Research Council 639776
6 · The paper itself

Abstract

backgroundDrugs and vaccines that can interrupt the transmission of Plasmodium falciparum will be important for malaria control and elimination. However, models for early clinical evaluation of candidate transmission-blocking interventions are currently unavailable. Here, we describe a new model for evaluating malaria transmission from humans to Anopheles mosquitoes using controlled human malaria infection (CHMI).

methodsSeventeen healthy malaria-naive volunteers underwent CHMI by intravenous inoculation of P. falciparum-infected erythrocytes to initiate blood-stage infection. Seven to eight days after inoculation, participants received piperaquine (480 mg) to attenuate asexual parasite replication while allowing gametocytes to develop and mature. Primary end points were development of gametocytemia, the transmissibility of gametocytes from humans to mosquitoes, and the safety and tolerability of the CHMI transmission model. To investigate in vivo gametocytocidal drug activity in this model, participants were either given an experimental antimalarial, artefenomel (500 mg), or a known gametocytocidal drug, primaquine (15 mg), or remained untreated during the period of gametocyte carriage.

resultsMale and female gametocytes were detected in all participants, and transmission to mosquitoes was achieved from 8 of 11 (73%) participants evaluated. Compared with results in untreated controls (n = 7), primaquine (15 mg, n = 5) significantly reduced gametocyte burden (P = 0.01), while artefenomel (500 mg, n = 4) had no effect. Adverse events (AEs) were mostly mild or moderate. Three AEs were assessed as severe - fatigue, elevated alanine aminotransferase, and elevated aspartate aminotransferase - and were attributed to malaria infection. Transaminase elevations were transient, asymptomatic, and resolved without intervention.

conclusionWe report the safe and reproducible induction of P. falciparum gametocytes in healthy malaria-naive volunteers at densities infectious to mosquitoes, thereby demonstrating the potential for evaluating transmission-blocking interventions in this model.

trial registrationClinicalTrials.gov NCT02431637 and NCT02431650.

fundingBill & Melinda Gates Foundation.

Indexed as

Malaria, FalciparumModels, BiologicalPlasmodium falciparumAdamantaneAdolescentAdultAnimalsAntimalarialsCulicidaeErythrocytesFemaleHumansMaleMiddle AgedPeroxidesPiperazinesAdamantaneAntimalarialsartefenomelPeroxidespiperaquinePiperazinesPrimaquineQuinolinesClinical TrialsInfectious diseaseMalaria

Identifiers

PMID29389671
PMCPMC5873858
OpenAlexW2786464058

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.