Evidence map›Paper›PMID 25193380›Full record

ReviewTranslational research : the journal of laboratory and clinical medicine2015

Epigenetic enzymes are the therapeutic targets for CD4(+)CD25(+/high)Foxp3(+) regulatory T cells.

Jahaira Lopez-Pastrana, Ying Shao, Valeria Chernaya, Hong Wang, Xiao-Feng Yang

Open access · greenAbstract readReview
In one paragraph

Review in Translational research : the journal of laboratory and clinical medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

28 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. EVs vs. EVs: MSCs and Tregs as a source of invisible possibilities.Journal of molecular medicine (Berlin, Germany) · 2023
    Review
  6. Article
  7. Article
  8. 29 mJournal of immunology research · 2022
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Coexpression of Helios in Foxp3Disease markers · 2021
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  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

5 authors at 1 institution in 1 country.

Jahaira Lopez-PastranaCenters for Metabolic Disease Research and Cardiovascular Research, Temple University School of Medicine, Philadelphia, Penn.
Ying ShaoCenters for Metabolic Disease Research and Cardiovascular Research, Temple University School of Medicine, Philadelphia, Penn.
Valeria ChernayaCenters for Metabolic Disease Research and Cardiovascular Research, Temple University School of Medicine, Philadelphia, Penn.
Hong WangCenters for Metabolic Disease Research and Cardiovascular Research, Temple University School of Medicine, Philadelphia, Penn.
Xiao-Feng YangCenters for Metabolic Disease Research and Cardiovascular Research, Temple University School of Medicine, Philadelphia, Penn; Department of Microbiology and Immunology, Temple University School of Medicine, Philadelphia, Penn. Electronic address: jahapastrana@gmail.com.
Temple University · US

Funding

Roles of Interleukin-17 in Endothelial CellsR01HL108910 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI YANG, XIAOFENG · 2011 to 2015
$1.9M
Suppression of vascular endothelial cell inflammationR01HL094451 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI YANG, XIAOFENG · 2009 to 2013
$1.8M
HHcy-induced Bax upregulation, Treg apoptosis and vascular diseaseR01HL116917 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI YANG, XIAOFENG · 2013 to 2016
$1.6M
NHLBI NIH HHS R01 HL094451NHLBI NIH HHS R01 HL108910NHLBI NIH HHS R01 HL116917
6 · The paper itself

Abstract

CD4(+)CD25(+/high)Foxp3(+) regulatory T (Treg) cells are a subset of CD4(+) T cells that play an essential role in maintaining peripheral immune tolerance. Several transcriptional cofactors have been recently identified, which form complexes with transcription factor Foxp3 of Treg cells and contribute in the suppressive function of Treg cells. However, Foxp3 is still defined as a "master" (multiple pathway) regulator gene that controls the development and stability of Treg cells. Because of its importance, the regulatory mechanisms underlying Foxp3 expression have been a focus of intensive investigation. Recent progress suggests that the epigenetic mechanisms responsible for regulating the Foxp3 gene expression are key components of suppressive activity of Treg cells. This review not only discusses the basic concepts of biology and epigenetic modifications of Treg cells, but also analyzes the translational clinical aspect of epigenetic modifications of Treg cells, focusing on several ongoing clinical trials and the Food and Drugs administration (FDA) approved epigenetic-based drugs. The new progress in identifying epigenetic enzymes functional in Treg cells is a new target for the development of novel therapeutic approaches for autoimmune and inflammatory diseases, graft-vs-host disease and cancers.

Indexed as

Epigenesis, GeneticAnimalsClinical Trials as TopicDNA MethylationForkhead Transcription FactorsHistone Deacetylase InhibitorsHistone DeacetylasesHistonesHumansInterleukin-2 Receptor alpha SubunitMicePeripheral ToleranceRNA, UntranslatedT-Lymphocytes, RegulatoryTranslational Research, BiomedicalForkhead Transcription FactorsFOXP3 protein, humanHistone Deacetylase InhibitorsHistone DeacetylasesHistonesIL2RA protein, humanInterleukin-2 Receptor alpha SubunitRNA, Untranslated

Identifiers

PMID25193380
PMCPMC4259825
OpenAlexW2024843655

What OpenQuestion holds

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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.