Evidence map›Paper›PMID 31572375›Full record

ArticleFrontiers in immunology2019

Tbet Expression in Regulatory T Cells Is Required to Initiate Th1-Mediated Colitis.

Martina Di Giovangiulio, Angelamaria Rizzo, Eleonora Franzè, Flavio Caprioli, Federica Facciotti, Sara Onali, Agnese Favale, Carmine Stolfi, Hans-Joerg Fehling, Giovanni Monteleone and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.4field-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

37 citing papers in PubMed, 58 citations in OpenAlex.

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  5. Cytokines Associated with Activation of CD4International journal of molecular sciences · 2026
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  14. Treg plasticity and human diseases.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Review
  15. Review
  16. Lung tumor-infiltrating TScience immunology · 2023
    Article
  17. Article
  18. Article
  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

11 authors at 3 institutions in 1 country.

Martina Di GiovangiulioDepartment of Systems Medicine, University of Rome "Tor Vergata", Rome, Italy.
Angelamaria RizzoDepartment of Systems Medicine, University of Rome "Tor Vergata", Rome, Italy.
Eleonora FranzèDepartment of Systems Medicine, University of Rome "Tor Vergata", Rome, Italy.
Flavio CaprioliGastroenterology and Endoscopy Unit, IRCCS Cà Granda Fundation, Ospedale Maggiore Policlinico, Milan, Italy.
Federica FacciottiDepartment of Experimental Oncology, IEO European Institute of Oncology IRCCS, Milan, Italy.
Sara OnaliDepartment of Biomedicine and Prevention, University of Rome "Tor Vergata", Rome, Italy.
Agnese FavaleDepartment of Systems Medicine, University of Rome "Tor Vergata", Rome, Italy.
Carmine StolfiDepartment of Systems Medicine, University of Rome "Tor Vergata", Rome, Italy.
Hans-Joerg FehlingInstitute of Immunology, University Clinics Ulm, Ulm, Germany.
Giovanni MonteleoneDepartment of Systems Medicine, University of Rome "Tor Vergata", Rome, Italy.
Massimo C FantiniDepartment of Systems Medicine, University of Rome "Tor Vergata", Rome, Italy.
University of Rome Tor Vergata · ITEuropean Institute of Oncology · ITOspedale Maggiore · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In normal conditions gut homeostasis is maintained by the suppressive activity of regulatory T cells (Tregs), characterized by the expression of the transcription factor FoxP3. In human inflammatory bowel disease, which is believed to be the consequence of the loss of tolerance toward antigens normally contained in the gut lumen, Tregs have been found to be increased and functionally active, thus pointing against their possible role in the pathogenesis of this immune-mediated disease. Though, in inflammatory conditions, Tregs have been shown to upregulate the T helper (Th) type 1-related transcription factor Tbet and to express the pro-inflammatory cytokine IFNγ, thus suggesting that at a certain point of the inflammatory process, Tregs might contribute to inflammation rather than suppress it. Starting from the observation that Tregs isolated from the lamina propria of active but not inactive IBD patients or uninflamed controls express Tbet and IFNγ, we investigated the functional role of Th1-like Tregs in the dextran sulfate model of colitis. As observed in human IBD, Th1-like Tregs were upregulated in the inflamed lamina propria of treated mice and the expression of Tbet and IFNγ in Tregs preceded the accumulation of conventional Th1 cells. By using a Treg-specific Tbet conditional knockout, we demonstrated that Tbet expression in Tregs is required for the development of colitis. Indeed, Tbet knockout mice developed milder colitis and showed an impaired Th1 immune response. In these mice not only the Tbet deficient Tregs but also the Tbet proficient conventional T cells showed reduced IFNγ expression. However, Tbet deficiency did not affect the Tregs suppressive capacity

Indexed as

AnimalsColitisFemaleGene Expression RegulationHumansInflammatory Bowel DiseasesMaleMiceT-bet Transcription FactorT-Box Domain ProteinsTh1 CellsT-Lymphocytes, RegulatoryT-bet Transcription FactorT-Box Domain Proteinsinflammationinflammatory bowel diseaseTbetTh1-like TregsTreg cells

Identifiers

PMID31572375
PMCPMC6749075
OpenAlexW2971333795

What OpenQuestion holds

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Registered trials

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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.