Evidence map›Paper›PMID 23129747›Full record

ArticleThe Journal of experimental medicine2012

Transcriptional regulator early growth response gene 2 (Egr2) is required for T cell anergy in vitro and in vivo.

Yan Zheng, Yuanyuan Zha, Gregory Driessens, Frederick Locke, Thomas F Gajewski

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

71 citing papers in PubMed, 104 citations in OpenAlex.

  1. Article
  2. Tumor-Associated Glycan Exploits Adenosine Receptor 2A Signaling to Facilitate Immune Evasion.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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  9. Tumor cell-derived spermidine is an oncometabolite that suppresses TCR clustering for intratumoral CD8Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  10. CARD19, a Novel Regulator of the TAK1/NF-κB Pathway in Self-Reactive B Cells.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Immune Aging and Immunotherapy in Cancer.International journal of molecular sciences · 2021
    Review
  18. Article
  19. Review
  20. Article

11 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

5 authors at 1 institution in 1 country.

Yan ZhengDepartment of Pathology and 2 Department of Medicine, University of Chicago, Chicago, IL 60637, USA.
Yuanyuan Zha
Gregory Driessens
Frederick Locke
Thomas F Gajewski
University of Chicago · US

Funding

EGR2 in T cell toleranceR01CA161005 · NCI · UNIVERSITY OF CHICAGO · PI GAJEWSKI, THOMAS F · 2012 to 2016
$1.6M
T Cell Responsiveness and Homeostasis in Anti-TumorR01CA118153 · NCI · UNIVERSITY OF CHICAGO · PI GAJEWSKI, THOMAS F · 2006 to 2010
$1.3M
DGK in T Cell Regulation and ToleranceR01AI080745 · NIAID · UNIVERSITY OF CHICAGO · PI GAJEWSKI, THOMAS F · 2009 to 2010
$780k
NCI NIH HHS R01 CA118153NCI NIH HHS R01 CA161005NIAID NIH HHS R01 AI080745
6 · The paper itself

Abstract

T cell receptor engagement in the absence of costimulation results in a hyporesponsive state termed anergy. Understanding the transcriptional regulation of other T cell differentiation states has provided critical information regarding the biology of T cell regulation in vivo. However, the transcriptional regulation of T cell anergy has been poorly understood. Using the key anergy target gene diacylglycerol kinase (DGK) α as a focal point, we identified early growth response gene 2 (Egr2) as a central transcription factor that regulates the anergic state. Conditional Egr2 deletion in peripheral T cells abolishes induced expression of DGK-α and other anergy genes and restores Ras/MAPK signaling, IL-2 production, and proliferation upon attempted anergy induction. Using superantigen- and tumor-induced anergy models, we found that Egr2 is necessary for anergy induction in vivo. Collectively, our results implicate Egr2 as an essential transcriptional regulator of the T cell anergy program.

Indexed as

Analysis of VarianceAnimalsBase SequenceChromatin ImmunoprecipitationClonal AnergyDiacylglycerol KinaseDNA PrimersEarly Growth Response Protein 2Flow CytometryGene Expression RegulationHumansImmunoblottingIn Vitro TechniquesLuciferasesMiceMolecular Sequence DataDiacylglycerol KinaseDNA PrimersEarly Growth Response Protein 2Egr2 protein, mouseLuciferases

Identifiers

PMID23129747
PMCPMC3501351
OpenAlexW2126753966

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.