Evidence map›Paper›PMID 28991267›Full record

ArticleNature immunology2017

Cytotoxic and regulatory roles of mucosal-associated invariant T cells in type 1 diabetes.

Ophélie Rouxel, Jennifer Da Silva, Lucie Beaudoin, Isabelle Nel, Céline Tard, Lucie Cagninacci, Badr Kiaf, Masaya Oshima, Marc Diedisheim, Marion Salou and 9 more

Erratum issued 2 registry-linked trialsAbstract read
In one paragraph

Article in Nature immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to 2 registered trials, which are not on this map. Cited by 142 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
142citing papers in PubMed, 1 pooled it
22.2field-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.

NCT05054361 recruitingnot on this mapstarted 2022, after this paper: background citation

Crosstalk Between Mucosal-Associated Invariant T Cells and the Gut Microbiota and Mucosa in the Development of Type 1 Diabetes in Children

TypeobservationalSponsorInstitut National de la Santé Et de la Recherche Médicale, FranceRan2022 to 2027Enrolled180ConditionsType1diabetesArmsMAIT cells analysis, MAIT cytokines production analysis, Lactulose/Mannitol Test, UGI Endoscopy, Coxsackie virus B infection status
NCT05176795 terminatednot on this mapstarted 2022, after this paper: background citation

Study of the Determinants of Pediatric Onset Inflammatory Diseases: Host-microbiota-environment Interactions

TypeobservationalSponsorUniversity Hospital, Clermont-FerrandRan2022 to 2022Enrolled4ConditionsJuvenile Idiopathic Arthritis, Diabetes type1, Inflammatory Bowel DiseasesArmsStool sample
3 · Its place in the literature

Who cites it

142 citing papers in PubMed, 1 synthesis or guideline pooled it, 245 citations in OpenAlex.

  1. Mucosal immune response in biology, disease prevention and treatment.Signal transduction and targeted therapy · 2025
    Pooled it
  2. Frontiers in endocrinology · 2023
    Trial
  3. Trial
  4. Trial
  5. Trial
  6. Review
  7. Gut archaea drive human MAIT cell responses.bioRxiv : the preprint server for biology · 2026
    Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Mucosal-Associated Invariant T Cells in Rheumatic Diseases.Arthritis & rheumatology (Hoboken, N.J.) · 2026
    Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 6 institutions in 4 countries.

Ophélie RouxelINSERM U1016, Institut Cochin, Paris, France, and Université Paris Descartes, Paris, France.
Jennifer Da SilvaINSERM U1016, Institut Cochin, Paris, France, and Université Paris Descartes, Paris, France.
Lucie BeaudoinINSERM U1016, Institut Cochin, Paris, France, and Université Paris Descartes, Paris, France.
Isabelle NelINSERM U1016, Institut Cochin, Paris, France, and Université Paris Descartes, Paris, France.
Céline TardINSERM U1016, Institut Cochin, Paris, France, and Université Paris Descartes, Paris, France.
Lucie CagninacciINSERM U1016, Institut Cochin, Paris, France, and Université Paris Descartes, Paris, France.
Badr KiafINSERM U1016, Institut Cochin, Paris, France, and Université Paris Descartes, Paris, France.
Masaya OshimaINSERM U1016, Institut Cochin, Paris, France, and Université Paris Descartes, Paris, France.
Marc DiedisheimINSERM U1016, Institut Cochin, Paris, France, and Université Paris Descartes, Paris, France.
Marion SalouINSERM U932, Institut Curie, Paris, France.
Alexandra CorbettInfection and Immunity Program and Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.ORCID http://orcid.org/0000-0003-1618-4337
Jamie RossjohnARC Centre of Excellence in Advanced Molecular Imaging, Monash University, Clayton, Victoria, Australia.
James McCluskeyInfection and Immunity Program and Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.ORCID http://orcid.org/0000-0002-8597-815X
Raphael ScharfmannINSERM U1016, Institut Cochin, Paris, France, and Université Paris Descartes, Paris, France.
Manuela BattagliaDiabetes Research Institute, IRCCS San Raffaele Scientific Institute, Milan, Italy, and TrialNet Clinical Center, San Raffaele Hospital, Milan, Italy.
Michel PolakINSERM U1016, Institut Cochin, Paris, France, and Université Paris Descartes, Paris, France.
Olivier LantzINSERM U932, Institut Curie, Paris, France.
Jacques BeltrandINSERM U1016, Institut Cochin, Paris, France, and Université Paris Descartes, Paris, France.
Agnès LehuenINSERM U1016, Institut Cochin, Paris, France, and Université Paris Descartes, Paris, France.ORCID http://orcid.org/0000-0002-0450-3321
Centre National de la Recherche Scientifique · FRAustralian Regenerative Medicine Institute · AUDélégation Paris 5 · FRInserm · FRThe University of Melbourne · AUVita-Salute San Raffaele University · IT

Funding

Type I Diabetes Trialnet at StsnfordU01DK061042 · NIDDK · STANFORD UNIVERSITY · PI WILSON, DARRELL M · 2001 to 2018
$8.5M
UCSF Trialnet: A Phase II Trial of Imatimib in New Onset Type I DiabetesU01DK061010 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GITELMAN, STEPHEN E · 2001 to 2018
$8.1M
Type 1 Diabetes-A Proposal for Prevention & InterventionU01DK085476 · NIDDK · UNIVERSITY OF MINNESOTA · PI MORAN, ANTOINETTE M. · 2009 to 2018
$7.1M
Type 1 Diabetes TrialNet at Indiana University Clinical CenterU01DK107014 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI DIMEGLIO, LINDA A · 2015 to 2018
$1.8M
Chicagoland Diabetes TrialNet Clinical CenterU01DK103153 · NIDDK · UNIVERSITY OF CHICAGO · PI PHILIPSON, LOUIS H. · 2014 to 2018
$1.4M
NIDDK NIH HHS U01 DK061010NIDDK NIH HHS U01 DK061042NIDDK NIH HHS U01 DK085476NIDDK NIH HHS U01 DK103153NIDDK NIH HHS U01 DK107014
6 · The paper itself

Abstract

Type 1 diabetes (T1D) is an autoimmune disease that results from the destruction of pancreatic β-cells by the immune system that involves innate and adaptive immune cells. Mucosal-associated invariant T cells (MAIT cells) are innate-like T-cells that recognize derivatives of precursors of bacterial riboflavin presented by the major histocompatibility complex (MHC) class I-related molecule MR1. Since T1D is associated with modification of the gut microbiota, we investigated MAIT cells in this pathology. In patients with T1D and mice of the non-obese diabetic (NOD) strain, we detected alterations in MAIT cells, including increased production of granzyme B, which occurred before the onset of diabetes. Analysis of NOD mice that were deficient in MR1, and therefore lacked MAIT cells, revealed a loss of gut integrity and increased anti-islet responses associated with exacerbated diabetes. Together our data highlight the role of MAIT cells in the maintenance of gut integrity and the control of anti-islet autoimmune responses. Monitoring of MAIT cells might represent a new biomarker of T1D, while manipulation of these cells might open new therapeutic strategies.

Indexed as

AnimalsCells, CulturedDiabetes Mellitus, Type 1Gastrointestinal MicrobiomeGranzymesHistocompatibility Antigens Class IHumansInsulin-Secreting CellsIntestinal MucosaMiceMice, Inbred C57BLMice, Inbred NODMinor Histocompatibility AntigensMucosal-Associated Invariant T CellsPancreasGranzymesHistocompatibility Antigens Class IMinor Histocompatibility AntigensMr1 protein, mouse

Identifiers

PMID28991267
PMCPMC6025738
OpenAlexW2760940233

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.