Evidence map›Paper›PMID 23053511›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2012

Bcl6 controls the Th2 inflammatory activity of regulatory T cells by repressing Gata3 function.

Deepali V Sawant, Sarita Sehra, Evelyn T Nguyen, Rohit Jadhav, Kate Englert, Ryo Shinnakasu, Giao Hangoc, Hal E Broxmeyer, Toshinori Nakayama, Narayanan B Perumal and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

63 citing papers in PubMed, 108 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Control of Asthma and Allergy by Regulatory T Cells.International archives of allergy and immunology · 2025
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Treg plasticity and human diseases.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

3 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

12 authors at 4 institutions in 2 countries.

Deepali V SawantDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN 46202, USA. adent2@iupui.edu
Sarita Sehra
Evelyn T Nguyen
Rohit Jadhav
Kate Englert
Ryo Shinnakasu
Giao Hangoc
Hal E Broxmeyer
Toshinori Nakayama
Narayanan B Perumal
Mark H Kaplan
Alexander L Dent
Indiana University – Purdue University Indianapolis · USIndiana University School of MedicineChiba University · JPUniversity of Indianapolis · US

Funding

Stat6 in Atopic DermatitisU19AI070448 · NIAID · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI KAPLAN, MARK H · 2006 to 2010
$5.1M
control of Inflammation by regulatory T cells and BCL6R21AI092297 · NIAID · INDIANA UNIVERSITY INDIANAPOLIS · PI DENT, ALEXANDER L · 2011 to 2012
$424k
Control of autoimmunity by follicular helper T cells and BCL6R21AI090150 · NIAID · INDIANA UNIVERSITY INDIANAPOLIS · PI DENT, ALEXANDER L · 2010 to 2011
$421k
Development of follicular helper T cell deficient miceR21AI099825 · NIAID · INDIANA UNIVERSITY INDIANAPOLIS · PI DENT, ALEXANDER L · 2012 to 2013
$415k
Control of Th2 and Th17 differentiation by BCL6R21AI079349 · NIAID · INDIANA UNIVERSITY INDIANAPOLIS · PI DENT, ALEXANDER L · 2009 to 2010
$385k
NIAID NIH HHS 1R21AI079349-01A1NIAID NIH HHS 1R21AI090150-01NIAID NIH HHS 1R21AI092212-01NIAID NIH HHS R21 AI079349NIAID NIH HHS R21 AI090150NIAID NIH HHS R21 AI092297NIAID NIH HHS R21 AI099825NIAID NIH HHS U19 AI070448
6 · The paper itself

Abstract

The transcriptional repressor Bcl6 is a critical arbiter of Th cell fate, promoting the follicular Th lineage while repressing other Th cell lineages. Bcl6-deficient (Bcl6(-/-)) mice develop a spontaneous and severe Th2-type inflammatory disease, thus warranting assessment of Bcl6 in regulatory T cell (Treg) function. Bcl6(-/-) Tregs were competent at suppressing T cell proliferation in vitro and Th1-type colitogenic T cell responses in vivo. In contrast, Bcl6(-/-) Tregs strongly exacerbated lung inflammation in a model of allergic airway disease and promoted higher Th2 responses, including systemic upregulation of microRNA-21. Further, Bcl6(-/-) Tregs were selectively impaired at controlling Th2 responses, but not Th1 and Th17 responses, in mixed chimeras of Bcl6(-/-) bone marrow with Foxp3(-/-) bone marrow. Bcl6(-/-) Tregs displayed increased levels of the Th2 transcription factor Gata3 and other Th2 and Treg genes. Bcl6 potently repressed Gata3 transcriptional transactivation, providing a mechanism for the increased expression of Th2 genes by Bcl6(-/-) Tregs. Gata3 has a critical role in regulating Foxp3 expression and functional fitness of Tregs; however, the signal that regulates Gata3 and restricts its transactivation of Th2 cytokines in Tregs has remained unexplored. Our results identify Bcl6 as an essential transcription factor regulating Gata3 activity in Tregs. Thus, Bcl6 represents a crucial regulatory layer in the Treg functional program that is required for specific suppression of Gata3 and Th2 effector responses by Tregs.

Indexed as

AnimalsCytokinesDNA-Binding ProteinsGATA3 Transcription FactorMiceMice, KnockoutMicroRNAsPneumoniaProto-Oncogene Proteins c-bcl-6Th17 CellsTh1 CellsTh2 CellsT-Lymphocytes, RegulatoryTranscriptional ActivationTranscription, GeneticBcl6 protein, mouseCytokinesDNA-Binding ProteinsGata3 protein, mouseGATA3 Transcription FactorMicroRNAsMIRN21 microRNA, mouseProto-Oncogene Proteins c-bcl-6

Identifiers

PMID23053511
PMCPMC3490013
OpenAlexW2116958080

What OpenQuestion holds

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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.