Evidence map›Paper›PMID 30862316›Full record

ArticleBMC medicine2019

Repeated clinical malaria episodes are associated with modification of the immune system in children.

Yaw Bediako, Rhys Adams, Adam J Reid, John Joseph Valletta, Francis M Ndungu, Jan Sodenkamp, Jedidah Mwacharo, Joyce Mwongeli Ngoi, Domtila Kimani, Oscar Kai and 14 more

Abstract read
In one paragraph

Article in BMC medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

47 citing papers in PubMed.

  1. Article
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  3. Observational
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  15. Regulatory T cell memory: implications for malaria.Journal of immunology (Baltimore, Md. : 1950) · 2025
    Review
  16. Article
  17. Article
  18. Article
  19. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors.

Yaw BediakoFrancis Crick Institute, London, UK.
Rhys AdamsFrancis Crick Institute, London, UK.
Adam J ReidWellcome Genome Campus, Wellcome Sanger Institute, Hinxton, Cambridgeshire, UK.
John Joseph VallettaUniversity of Exeter, Exeter, UK.
Francis M NdunguKEMRI/Wellcome Trust Research Programme, Kilifi, Kenya.
Jan SodenkampFrancis Crick Institute, London, UK.
Jedidah MwacharoKEMRI/Wellcome Trust Research Programme, Kilifi, Kenya.
Joyce Mwongeli NgoiKEMRI/Wellcome Trust Research Programme, Kilifi, Kenya.
Domtila KimaniKEMRI/Wellcome Trust Research Programme, Kilifi, Kenya.
Oscar KaiKEMRI/Wellcome Trust Research Programme, Kilifi, Kenya.
Juliana WambuaKEMRI/Wellcome Trust Research Programme, Kilifi, Kenya.
George NyangwesoKEMRI/Wellcome Trust Research Programme, Kilifi, Kenya.
Etienne P de VilliersKEMRI/Wellcome Trust Research Programme, Kilifi, Kenya.
Mandy SandersWellcome Genome Campus, Wellcome Sanger Institute, Hinxton, Cambridgeshire, UK.
Magda Ewa LotkowskaWellcome Genome Campus, Wellcome Sanger Institute, Hinxton, Cambridgeshire, UK.
Jing-Wen LinFrancis Crick Institute, London, UK.
Sarah ManniFrancis Crick Institute, London, UK.
John W G AddyFrancis Crick Institute, London, UK.
Mario ReckerUniversity of Exeter, Exeter, UK.
Chris NewboldWellcome Genome Campus, Wellcome Sanger Institute, Hinxton, Cambridgeshire, UK.
Matthew BerrimanWellcome Genome Campus, Wellcome Sanger Institute, Hinxton, Cambridgeshire, UK.
Philip BejonKEMRI/Wellcome Trust Research Programme, Kilifi, Kenya.
Kevin MarshNuffield Department of Medicine, University of Oxford, Oxford, UK.
Jean LanghorneFrancis Crick Institute, London, UK. jean.langhorne@crick.ac.uk.

Funding

Medical Research Council MR/M003906/1Medical Research Council MR/P020321/1Wellcome TrustWellcome Trust WT 206194
6 · The paper itself

Abstract

backgroundThere are over 200 million reported cases of malaria each year, and most children living in endemic areas will experience multiple episodes of clinical disease before puberty. We set out to understand how frequent clinical malaria, which elicits a strong inflammatory response, affects the immune system and whether these modifications are observable in the absence of detectable parasitaemia.

methodsWe used a multi-dimensional approach comprising whole blood transcriptomic, cellular and plasma cytokine analyses on a cohort of children living with endemic malaria, but uninfected at sampling, who had been under active surveillance for malaria for 8 years. Children were categorised into two groups depending on the cumulative number of episodes experienced: high (≥ 8) or low (< 5).

resultsWe observe that multiple episodes of malaria are associated with modification of the immune system. Children who had experienced a large number of episodes demonstrated upregulation of interferon-inducible genes, a clear increase in circulating levels of the immunoregulatory cytokine IL-10 and enhanced activation of neutrophils, B cells and CD8

conclusionTranscriptomic analysis together with cytokine and immune cell profiling of peripheral blood can robustly detect immune differences between children with different numbers of prior malaria episodes. Multiple episodes of malaria are associated with modification of the immune system in children. Such immune modifications may have implications for the initiation of subsequent immune responses and the induction of vaccine-mediated protection.

Indexed as

ChildChild, PreschoolHumansImmune System DiseasesMalariaImmune activationMalariaSystems immunology

Identifiers

PMID30862316
PMCPMC6415347

What OpenQuestion holds

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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.