Evidence map›Paper›PMID 26090605›Full record

ArticleScientific reports2015

EZH2 is crucial for both differentiation of regulatory T cells and T effector cell expansion.

Xiang-Ping Yang, Kan Jiang, Kiyoshi Hirahara, Golnaz Vahedi, Behdad Afzali, Giuseppe Sciume, Michael Bonelli, Hong-Wei Sun, Dragana Jankovic, Yuka Kanno and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

102 citing papers in PubMed, 146 citations in OpenAlex.

  1. Review
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  4. International journal of molecular sciences · 2026
    Review
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  7. Review
  8. Article
  9. Article
  10. Article
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  13. Review
  14. Mechanisms and Therapeutic Implications of EZH2 in Nasal Diseases.Clinical reviews in allergy & immunology · 2025
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

42 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

13 authors at 5 institutions in 3 countries.

Xiang-Ping Yang1] Department of Immunology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China [2] Lymphocyte Cell Biology Section, Molecular Immunology and Inflammation Branch National Institutes of Arthritis, and Musculoskeletal and Skin Diseases National Institutes of Health, Bethesda, MD 20892, USA.
Kan JiangLymphocyte Cell Biology Section, Molecular Immunology and Inflammation Branch National Institutes of Arthritis, and Musculoskeletal and Skin Diseases National Institutes of Health, Bethesda, MD 20892, USA.
Kiyoshi HiraharaLymphocyte Cell Biology Section, Molecular Immunology and Inflammation Branch National Institutes of Arthritis, and Musculoskeletal and Skin Diseases National Institutes of Health, Bethesda, MD 20892, USA.
Golnaz VahediLymphocyte Cell Biology Section, Molecular Immunology and Inflammation Branch National Institutes of Arthritis, and Musculoskeletal and Skin Diseases National Institutes of Health, Bethesda, MD 20892, USA.
Behdad Afzali1] Lymphocyte Cell Biology Section, Molecular Immunology and Inflammation Branch National Institutes of Arthritis, and Musculoskeletal and Skin Diseases National Institutes of Health, Bethesda, MD 20892, USA [2] MRC Centre for Transplantation, King's College London, UK.
Giuseppe SciumeLymphocyte Cell Biology Section, Molecular Immunology and Inflammation Branch National Institutes of Arthritis, and Musculoskeletal and Skin Diseases National Institutes of Health, Bethesda, MD 20892, USA.
Michael BonelliLymphocyte Cell Biology Section, Molecular Immunology and Inflammation Branch National Institutes of Arthritis, and Musculoskeletal and Skin Diseases National Institutes of Health, Bethesda, MD 20892, USA.
Hong-Wei SunBiodata Mining and Discovery Section, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892-1930, USA.
Dragana JankovicImmunobiology Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases.
Yuka KannoLymphocyte Cell Biology Section, Molecular Immunology and Inflammation Branch National Institutes of Arthritis, and Musculoskeletal and Skin Diseases National Institutes of Health, Bethesda, MD 20892, USA.
Vittorio SartorelliLaboratory of Muscle Stem Cells and Gene Regulation, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892-1930, USA.
John J O'SheaLymphocyte Cell Biology Section, Molecular Immunology and Inflammation Branch National Institutes of Arthritis, and Musculoskeletal and Skin Diseases National Institutes of Health, Bethesda, MD 20892, USA.
Arian Laurence1] Northern Centre for cancer care, Freeman hospital, Newcastle upon tyne, UK [2] NDM Experimental medicine, John Radcliffe hospital, Oxford, UK.
National Institute of Arthritis and Musculoskeletal and Skin Diseases · USNational Institutes of Health · USFreeman Hospital · GBHuazhong University of Science and Technology · CNNational Institute of Allergy and Infectious Diseases · US

Funding

Stat transcription factors in immunoregulation and autoimmune diseaseZIAAR041159 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI O'SHEA, JOHN · 2009 to 2025
$49.3M
SIRT1 in Skeletal Muscle Development, Regeneration, and AtrophyZIAAR041164 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI SARTORELLI, VITTORIO · 2009 to 2025
$15.3M
Applying Bioinformatics to Research in Immune, Muscle, and Bone DiseasesZIHAR041173 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI GADINA, MASSIMO · 2009 to 2020
$11.0M
Immune Regulation In Toxoplasmosis And Other Opportunistic InfectionsZIAAI000579 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI SHER, ALAN · 2009 to 2022
$7.8M
Intramural NIH HHSWellcome Trust
6 · The paper itself

Abstract

The roles of EZH2 in various subsets of CD4(+) T cells are controversial and its mechanisms of action are incompletely understood. FOXP3-positive Treg cells are a critical helper T cell subset, and dysregulation of Treg generation or function results in systemic autoimmunity. FOXP3 associates with EZH2 to mediate gene repression and suppressive function. Herein, we demonstrate that deletion of Ezh2 in CD4 T cells resulted in reduced numbers of Treg cells in vivo and differentiation in vitro and an increased proportion of memory CD4 T cells in part due to exaggerated production of effector cytokines. Furthermore, we found that both Ezh2-deficient Treg cells and T effector cells were functionally impaired in vivo: Tregs failed to constrain autoimmune colitis and T effector cells neither provided a protective response to T. gondii infection nor mediated autoimmune colitis. The dichotomous function of EZH2 in regulating differentiation and senescence in effector and regulatory T cells helps to explain the apparent existing contradictions in literature.

Indexed as

AnimalsAutoimmune DiseasesCell DifferentiationColitisCytokinesEnhancer of Zeste Homolog 2 ProteinGene Expression RegulationMiceMice, KnockoutPolycomb Repressive Complex 2T-Lymphocytes, RegulatoryCytokinesEnhancer of Zeste Homolog 2 ProteinEzh2 protein, mousePolycomb Repressive Complex 2

Identifiers

PMID26090605
PMCPMC4473539
OpenAlexW2260219310

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.