Evidence map›Paper›PMID 26811641›Full record

ReviewWorld journal of gastroenterology2016

Disrupted regulatory T cell homeostasis in inflammatory bowel diseases.

Christophe Pedros, Fanny Duguet, Abdelhadi Saoudi, Marianne Chabod

Open access · hybridAbstract readReview
In one paragraph

Review in World journal of gastroenterology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
3.3field-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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Regulatory T Cell Dysfunction in Autoimmune Diseases.International journal of molecular sciences · 2024
    Review
  9. Article
  10. Article
  11. Nutrients · 2023
    Article
  12. Enhancing Regulatory T Cells to Treat Inflammatory and Autoimmune Diseases.International journal of molecular sciences · 2023
    Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. 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

4 authors at 1 institution in 1 country.

Christophe PedrosChristophe Pedros, Division of Cell Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92307, United States.
Fanny DuguetChristophe Pedros, Division of Cell Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92307, United States.
Abdelhadi SaoudiChristophe Pedros, Division of Cell Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92307, United States.
Marianne ChabodChristophe Pedros, Division of Cell Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92307, United States.
La Jolla Institute for Immunology · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the gut, where billions of non-self-antigens from the food and the microbiota are present, the immune response must be tightly regulated to ensure both host protection against pathogenic microorganisms and the absence of immune-related pathologies. It has been well documented that regulatory T cells (Tregs) play a pivotal role in this context. Indeed, Tregs are able to prevent excessive inflammation, which can lead to the rupture of intestinal homeostasis observed in inflammatory bowel diseases (IBDs). Both the worldwide incidence and prevalence of such diseases have increased throughout the latter part of the 20(th) century. Therefore, it is crucial to understand how Tregs suppress the colitogenic immune cells to establish new treatments for patients suffering from IBDs. In this review, we will first summarize the results obtained in animal model studies that highlight the importance of Tregs in maintaining intestinal homeostasis and describe the specific suppressive mechanisms involved. Next, our current knowledge about Tregs contribution to human IBDs will be reviewed, as well as the current therapeutic perspective on using Tregs for clinical IBD treatment and the challenges that remain to be resolved to ensure both the safety and effectiveness of these therapies in targeting this critical immune-regulatory cell population.

Indexed as

AnimalsGastrointestinal AgentsGastrointestinal MicrobiomeHomeostasisHost-Pathogen InteractionsHumansImmunosuppressive AgentsImmunotherapyInflammation MediatorsInflammatory Bowel DiseasesIntestinal MucosaIntestinesPhenotypeT-Lymphocytes, RegulatoryGastrointestinal AgentsImmunosuppressive AgentsInflammation MediatorsColitisFoxp3GutInflammatory bowel diseaseRegulatory T cells

Identifiers

PMID26811641
PMCPMC4716049
OpenAlexW2412372355

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.