Evidence map›Paper›PMID 26191063›Full record

ReviewFrontiers in immunology2015

iNKT and MAIT Cell Alterations in Diabetes.

Isabelle Magalhaes, Badr Kiaf, Agnès Lehuen

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

27 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Protective effects ofFrontiers in pharmacology · 2024
    Article
  5. Dysfunction of circulating CD3International journal of medical sciences · 2023
    Article
  6. Development of αβ T Cells with Innate Functions.Advances in experimental medicine and biology · 2022
    Article
  7. Involvement of impaired CD8Reproductive biology and endocrinology : RB&E · 2021
    Article
  8. Impact of Bariatric Surgery on Adipose Tissue Biology.Journal of clinical medicine · 2021
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. CD4Reproductive biology and endocrinology : RB&E · 2019
    Article
  16. Mucosal-associated invariant T cells and disease.Nature reviews. Immunology · 2019
    Review
  17. Review
  18. Review
  19. Article
  20. Review
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

3 authors at 2 institutions in 1 country.

Isabelle MagalhaesINSERM U1016, Institut Cochin , Paris , France ; UMR8104, CNRS , Paris , France ; Laboratoire d'Excellence INFLAMEX, Université Paris Descartes, Sorbonne Paris Cité , Paris , France.
Badr KiafINSERM U1016, Institut Cochin , Paris , France ; UMR8104, CNRS , Paris , France ; Laboratoire d'Excellence INFLAMEX, Université Paris Descartes, Sorbonne Paris Cité , Paris , France.
Agnès LehuenINSERM U1016, Institut Cochin , Paris , France ; UMR8104, CNRS , Paris , France ; Laboratoire d'Excellence INFLAMEX, Université Paris Descartes, Sorbonne Paris Cité , Paris , France ; Département de Diabétologie, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris , Paris , France.
Centre National de la Recherche Scientifique · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 1 diabetes (T1D) and type 2 diabetes (T2D) are multifactorial diseases with different etiologies in which chronic inflammation takes place. Defects in invariant natural killer T (iNKT) cell populations have been reported in both T1D and T2D patients, mouse models and our recent study revealed mucosal-associated invariant T (MAIT) cell defects in T2D and obese patients. Regarding iNKT cells many studies in non-obese diabetic mice demonstrated their protective role against T1D whereas their potential role in human T1D is still under debate. Studies in mouse models and patients suggest that iNKT cells present in adipose tissue (AT) could exert a regulatory role against obesity and associated metabolic disorders, such as T2D. Scarce data are yet available on MAIT cells; however, we recently described MAIT cell abnormalities in the blood and ATs from obese and T2D patients. These data show that a link between MAIT cells and metabolic disorders pave the way for further investigations on MAIT cells in T1D and T2D in humans and mouse models. Furthermore, we hypothesize that the gut microbiota alterations associated with T1D and T2D could modulate iNKT and MAIT cell frequency and functions. The potential role of iNKT and MAIT cells in the regulation of metabolic pathways and their cross-talk with microbiota represent exciting new lines of research.

Indexed as

iNKT cellsMAIT cellsmicrobiotaobesityT1DT2D

Identifiers

PMID26191063
PMCPMC4489333
OpenAlexW1855962337

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.