Evidence map›Paper›PMID 36594463›Full record

ArticleThe Journal of clinical investigation2023

IL-10-producing Th1 cells possess a distinct molecular signature in malaria

Chelsea L Edwards, Susanna S Ng, Fabian de Labastida Rivera, Dillon Corvino, Jessica A Engel, Marcela Montes de Oca, Luzia Bukali, Teija Cm Frame, Patrick T Bunn, Shashi Bhushan Chauhan and 18 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
10.7field-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.

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

34 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The LEF1-LAG3 axis regulates CD4Parasites & vectors · 2026
    Article
  5. Article
  6. Review
  7. Article
  8. T-bet-expressing Tr1 cells driven by dietary signals dominate the small intestinal immune landscape.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Regulatory T cell memory: implications for malaria.Journal of immunology (Baltimore, Md. : 1950) · 2025
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors at 7 institutions in 5 countries.

Chelsea L EdwardsQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Susanna S NgQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Fabian de Labastida RiveraQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Dillon CorvinoQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Jessica A EngelQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Marcela Montes de OcaQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Luzia BukaliQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Teija Cm FrameQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Patrick T BunnQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Shashi Bhushan ChauhanDepartment of Medicine, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.
Siddharth Sankar SinghDepartment of Medicine, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.
Yulin WangQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Jinrui NaQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Fiona H AmanteQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Jessica R LoughlandQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Megan Sf SoonQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Nicola WaddellQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Pamela MukhopadhayQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Lambros T KoufariotisQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Rebecca L JohnstonQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Jason S LeeQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Rachel KunsQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Ping ZhangQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Michelle J BoyleQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Geoffrey R HillClinical Research Division, Fred Hutchinson Cancer Research Centre, Seattle, Washington, USA.
James S McCarthyQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Rajiv KumarCentre of Experimental Medicine and Surgery, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.
Christian R EngwerdaQIMR Berghofer Medical Research Institute, Brisbane, Australia.
QIMR Berghofer Medical Research Institute · AUThe University of Queensland · AUInstitute of Medical Sciences · INGriffith University · AUFred Hutch Cancer Center · USThe University of Melbourne · AUUniversity of Bonn · DE

Funding

Visceral Leishmaniasis in Bihar State, IndiaU19AI074321 · NIAID · BANARAS HINDU UNIVERSITY · PI SUNDAR, SHYAM · 2017 to 2021
$2.8M
NIAID NIH HHS U19 AI074321Wellcome Trust
6 · The paper itself

Abstract

Control of intracellular parasites responsible for malaria requires host IFN-γ+T-bet+CD4+ T cells (Th1 cells) with IL-10 produced by Th1 cells to mitigate the pathology induced by this inflammatory response. However, these IL-10-producing Th1 (induced type I regulatory [Tr1]) cells can also promote parasite persistence or impair immunity to reinfection or vaccination. Here, we identified molecular and phenotypic signatures that distinguished IL-10-Th1 cells from IL-10+Tr1 cells in Plasmodium falciparum-infected people who participated in controlled human malaria infection studies, as well as C57BL/6 mice with experimental malaria caused by P. berghei ANKA. We also identified a conserved Tr1 cell molecular signature shared between patients with malaria, dengue, and graft-versus-host disease. Genetic manipulation of primary human CD4+ T cells showed that the transcription factor cMAF played an important role in the induction of IL-10, while BLIMP-1 promoted the development of human CD4+ T cells expressing multiple coinhibitory receptors. We also describe heterogeneity of Tr1 cell coinhibitory receptor expression that has implications for targeting these molecules for clinical advantage during infection. Overall, this work provides insights into CD4+ T cell development during malaria that offer opportunities for creation of strategies to modulate CD4+ T cell functions and improve antiparasitic immunity.

Indexed as

MalariaT-Lymphocytes, RegulatoryAnimalsCD4-Positive T-LymphocytesHumansInterleukin-10MiceMice, Inbred C57BLTh1 CellsInterleukin-10ImmunologyInfectious diseaseTh1 response

Identifiers

PMID36594463
PMCPMC9797345
OpenAlexW4313427306

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.