Evidence map›Paper›PMID 33049000›Full record

ArticlePLoS pathogens2020

IL-27 signalling regulates glycolysis in Th1 cells to limit immunopathology during infection.

Marcela Montes de Oca, Fabian de Labastida Rivera, Clay Winterford, Teija C M Frame, Susanna S Ng, Fiona H Amante, Chelsea L Edwards, Luzia Bukali, Yulin Wang, Jude E Uzonna and 7 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

23 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. EomesoderminImmunity · 2025
    Article
  5. Regulatory T cell memory: implications for malaria.Journal of immunology (Baltimore, Md. : 1950) · 2025
    Review
  6. Article
  7. Article
  8. Modulation of Macrophages TLR4-Mediated Transcriptional Response byInternational journal of molecular sciences · 2025
    Article
  9. The influence of interleukin-27 on metabolic fitness in a murine neonatal model of bacterial sepsis.American journal of physiology. Endocrinology and metabolism · 2025
    Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. The role of CD4Frontiers in cellular and infection microbiology · 2024
    Review
  15. Article
  16. Article
  17. Role of IL-27 in HSV-1-Induced Herpetic Stromal Keratitis.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Article
  18. Article
  19. Foods (Basel, Switzerland) · 2022
    Article
  20. Article
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

17 authors at 4 institutions in 4 countries.

Marcela Montes de OcaImmunology and Infection Laboratory, Infectious Diseases Division, QIMR Berghofer Medical Research Institute, Brisbane, Australia.ORCID 0000-0003-1152-6158
Fabian de Labastida RiveraImmunology and Infection Laboratory, Infectious Diseases Division, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Clay WinterfordQIMR Berghofer Histology Facility, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Teija C M FrameImmunology and Infection Laboratory, Infectious Diseases Division, QIMR Berghofer Medical Research Institute, Brisbane, Australia.ORCID 0000-0002-0937-4231
Susanna S NgImmunology and Infection Laboratory, Infectious Diseases Division, QIMR Berghofer Medical Research Institute, Brisbane, Australia.ORCID 0000-0002-8494-7722
Fiona H AmanteImmunology and Infection Laboratory, Infectious Diseases Division, QIMR Berghofer Medical Research Institute, Brisbane, Australia.ORCID 0000-0002-7788-5885
Chelsea L EdwardsImmunology and Infection Laboratory, Infectious Diseases Division, QIMR Berghofer Medical Research Institute, Brisbane, Australia.ORCID 0000-0002-5881-263X
Luzia BukaliImmunology and Infection Laboratory, Infectious Diseases Division, QIMR Berghofer Medical Research Institute, Brisbane, Australia.ORCID 0000-0003-1743-8570
Yulin WangImmunology and Infection Laboratory, Infectious Diseases Division, QIMR Berghofer Medical Research Institute, Brisbane, Australia.ORCID 0000-0002-9976-5315
Jude E UzonnaDepartment of Immunology, College of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
Rachel D KunsBone Marrow Transplantation Laboratory, Cancer Division, QIMR Berghofer Medical Research Institute, Brisbane, Australia.ORCID 0000-0002-7465-7262
Ping ZhangBone Marrow Transplantation Laboratory, Cancer Division, QIMR Berghofer Medical Research Institute, Brisbane, Australia.ORCID 0000-0002-0311-6725
Agnieszka KabatMax Plank Institute of Immunobiology and Epigenetics, Freiburg, Germany.ORCID 0000-0003-1916-5983
Ramon I Klein GeltinkMax Plank Institute of Immunobiology and Epigenetics, Freiburg, Germany.ORCID 0000-0003-4610-3059
Edward J PearceMax Plank Institute of Immunobiology and Epigenetics, Freiburg, Germany.
Geoffrey R HillClinical Research Division, Fred Hutchinson Cancer Research Centre, Washington, United States of America.
Christian R EngwerdaImmunology and Infection Laboratory, Infectious Diseases Division, QIMR Berghofer Medical Research Institute, Brisbane, Australia.ORCID 0000-0003-2813-4804
QIMR Berghofer Medical Research Institute · AUMax Planck Institute of Immunobiology and Epigenetics · DEFred Hutch Cancer Center · USUniversity of Manitoba · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammation is critical for controlling pathogens, but also responsible for symptoms of infectious diseases. IL-27 is an important regulator of inflammation and can limit development of IFNγ-producing Tbet+ CD4+ T (Th1) cells. IL-27 is thought to do this by stimulating IL-10 production by CD4+ T cells, but the underlying mechanisms of these immunoregulatory pathways are not clear. Here we studied the role of IL-27 signalling in experimental visceral leishmaniasis (VL) caused by infection of C57BL/6 mice with the human pathogen Leishmania donovani. We found IL-27 signalling was critical for the development of IL-10-producing Th1 (Tr1) cells during infection. Furthermore, in the absence of IL-27 signalling, there was improved control of parasite growth, but accelerated splenic pathology characterised by the loss of marginal zone macrophages. Critically, we discovered that IL-27 signalling limited glycolysis in Th1 cells during infection that in turn attenuated inflammation. Furthermore, the modulation of glycolysis in the absence of IL-27 signalling restricted tissue pathology without compromising anti-parasitic immunity. Together, these findings identify a novel mechanism by which IL-27 mediates immune regulation during disease by regulating cellular metabolism.

Indexed as

AnimalsCD4-Positive T-LymphocytesFemaleGlycolysisInterferon-gammaInterleukinsLeishmania donovaniLeishmaniasis, VisceralMacrophagesMiceMice, Inbred C57BLSignal TransductionSpleenTh1 CellsIl27 protein, mouseInterferon-gammaInterleukins

Identifiers

PMID33049000
PMCPMC7584222
OpenAlexW3092323366

What OpenQuestion holds

Textmetadata
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.