Evidence map›Paper›PMID 23656897›Full record

ReviewInflammatory bowel diseases2013

Induced and natural regulatory T cells in the development of inflammatory bowel disease.

Christopher G Mayne, Calvin B Williams

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Inflammatory bowel diseases, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04691232 (Phase I, Open-label, Fast-track Dose-escalation Clinical Trial Exploring the Safety and the Tolerability of Autologous ex Vivo Expanded Regulatory T Cells in Adults With Ulcerative Colitis), which is not on this map. Cited by 91 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% 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.

NCT04691232 phase1completednot on this mapstarted 2021, after this paper: background citation

Phase I, Open-label, Fast-track Dose-escalation Clinical Trial Exploring the Safety and the Tolerability of Autologous ex Vivo Expanded Regulatory T Cells in Adults With Ulcerative Colitis

TypeinterventionalSponsorUniversity of Erlangen-Nürnberg Medical SchoolRan2021 to 2023Enrolled11ConditionsUlcerative Colitis, Autoimmune DiseasesArmsRegulatory T cells
3 · Its place in the literature

Who cites it

91 citing papers in PubMed, 1 synthesis or guideline pooled it, 170 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Review
  7. T Regulatory Cells in Inflammatory Bowel Disease-Are They Major Players?International journal of molecular sciences · 2025
    Review
  8. Article
  9. Article
  10. OGG1 augments the transcriptional activation ofProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Foods (Basel, Switzerland) · 2023
    Article
  17. Article
  18. Article
  19. Article
  20. Inflammatory Bowel Diseases and Gut Microbiota.International journal of molecular sciences · 2023
    Review

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

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

2 authors at 1 institution in 1 country.

Christopher G MayneSection of Rheumatology, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Calvin B Williams
Medical College of Wisconsin · US

Funding

Mechanisms of Disease Pathogenesis in Regulatory T cell DeficiencyR01AI085090 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHATILA, TALAL AMINE, WILLIAMS, CALVIN B · 2010 to 2020
$3.9M
Regulatory T Cell Selection and SpecificityR01AI073731 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI CHATILA, TALAL AMINE, WILLIAMS, CALVIN B · 2009 to 2010
$986k
CM F32 12-08-10 ResubmissionF32AI092977 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI MAYNE, CHRISTOPHER GARY · 2011 to 2013
$170k
NIAID NIH HHS F32 AI092977NIAID NIH HHS R01 AI073731NIAID NIH HHS R01 AI085090
6 · The paper itself

Abstract

The mucosal immune system mediates contact between the host and the trillions of microbes that symbiotically colonize the gastrointestinal tract. Failure to tolerate the antigens within this "extended self" can result in inflammatory bowel disease (IBD). Within the adaptive immune system, the most significant cells modulating this interaction are Foxp3 regulatory T (Treg) cells. Treg cells can be divided into 2 primary subsets: "natural" Treg cells and "adaptive" or "induced" Treg. Recent research suggests that these subsets serve to play both independent and synergistic roles in mucosal tolerance. Studies from both mouse models and human patients suggest that defects in Treg cells can play distinct causative roles in IBD. Numerous genetic, microbial, nutritional, and environmental factors that associate with IBD may also affect Treg cells. In this review, we summarize the development and function of Treg cells and how their regulatory mechanisms may fail, leading to a loss of mucosal tolerance. We discuss both animal models and studies of patients with IBD suggesting Treg cell involvement in IBD and consider how Treg cells may be used in future therapies.

Indexed as

Immune ToleranceAnimalsDisease Models, AnimalForkhead Transcription FactorsHumansInflammatory Bowel DiseasesMiceT-Lymphocytes, RegulatoryForkhead Transcription Factors

Identifiers

PMID23656897
PMCPMC3690174
OpenAlexW2073701525

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.