Evidence map›Paper›PMID 37819474›Full record

ReviewAmino acids2023

Mucosal-associated invariant T cells display both pathogenic and protective roles in patients with inflammatory bowel diseases.

Lei Wei, Zhigang Chen, Qiang Lv

Abstract readReview
PubMed Publisher
In one paragraph

Review in Amino acids, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 34% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

3 authors at 1 institution in 1 country.

Lei Wei *Department of General Surgery, Pudong New District Gongli Hospital of Shanghai, Shanghai, 200120, China.
Zhigang Chen *Department of General Surgery, Pudong New District Gongli Hospital of Shanghai, Shanghai, 200120, China.
Qiang LvDepartment of General Surgery, Pudong New District Gongli Hospital of Shanghai, Shanghai, 200120, China. ivqiangsina@gmail.com.ORCID http://orcid.org/0009-0004-8061-2660
Second Military Medical University · CN

Funding

Project of Shanghai New District Health Commission PW2021A-25
6 · The paper itself

Abstract

An important subtype of the innate-like T lymphocytes is mucosal-associated invariant T (MAIT) cells expressing a semi-invariant T cell receptor α (TCR-α) chain. MAIT cells could be activated mainly by TCR engagement or cytokines. They have been found to have essential roles in various immune mediated. There have been growing preclinical and clinical findings that show an association between MAIT cells and the physiopathology of inflammatory bowel diseases (IBD). Of note, published reports demonstrate contradictory findings regarding the role of MAIT cells in IBD patients. A number of reports suggests a protective effect, whereas others show a pathogenic impact. The present review article aimed to explore and discuss the findings of experimental and clinical investigations evaluating the effects of MAIT cells in IBD subjects and animal models. Findings indicate that MAIT cells could exert opposite effects in the course of IBD, including an anti-inflammatory protective effect of blood circulating MAIT cells and an effector pathogenic effect of colonic MAIT cells. Another important finding is that blood levels of MAIT cells can be considered as a potential biomarker in IBD patients.

Indexed as

Inflammatory Bowel DiseasesMucosal-Associated Invariant T CellsAnimalsBiomarkersCytokinesHumansReceptors, Antigen, T-Cell, alpha-betaBiomarkersCytokinesReceptors, Antigen, T-Cell, alpha-betaCrohn’s diseaseInflammatory bowel diseaseMAIT cellUlcerative colitis

Identifiers

PMID37819474
OpenAlexW4387528578

What OpenQuestion holds

Textmetadata
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.