Evidence map›Paper›PMID 19648923›Full record

ArticleNature immunology2009

T cell factor 1 initiates the T helper type 2 fate by inducing the transcription factor GATA-3 and repressing interferon-gamma.

Qing Yu, Archna Sharma, Sun Young Oh, Hyung-Geun Moon, M Zulfiquer Hossain, Theresa M Salay, Karen E Leeds, Hansen Du, Beibei Wu, Marian L Waterman and 2 more

Open access · greenAbstract read
In one paragraph

Article in Nature immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 135 papers.

0numbers the graph read from it
0cells of the map it votes in
135citing papers in PubMed
5.6field-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

135 citing papers in PubMed, 202 citations in OpenAlex.

  1. Targeting BCL9/BCL9L enhances CD4Acta pharmacologica Sinica · 2026
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  4. Prostaglandin IThe Journal of allergy and clinical immunology · 2025
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  5. Observational
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  7. Refining Diagnostic Subtypes of Peripheral T-Cell Lymphoma Using a Multiparameter Approach.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2025
    Article
  8. CD4Frontiers in immunology · 2025
    Review
  9. Autoimmune CD4Immunity · 2024
    Article
  10. Review
  11. Article
  12. Review
  13. The role of CD4Frontiers in cellular and infection microbiology · 2024
    Review
  14. T cells in health and disease.Signal transduction and targeted therapy · 2023
    Review
  15. Review
  16. Identification of a unique subset of tissue-resident memory CD4Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  17. Identification of the novel FOXP3-dependent TFrontiers in immunology · 2023
    Article
  18. Article
  19. Article
  20. Article

75 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 5 institutions in 1 country.

Qing YuLymphocyte Development Unit, Laboratory of Immunology, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, USA.
Archna Sharma
Sun Young Oh
Hyung-Geun Moon
M Zulfiquer Hossain
Theresa M Salay
Karen E Leeds
Hansen Du
Beibei Wu
Marian L Waterman
Zhou Zhu
Jyoti Misra Sen
National Institute on Aging · USJohns Hopkins University · USNational Institutes of Health · USUniversity of California, Irvine · USJohns Hopkins Medicine · US

Funding

T Cell factor-1 and beta-catenin regulate the development of innate and conventional cells in the thymusZIAAG000772 · NIA · NATIONAL INSTITUTE ON AGING · PI SEN, JYOTI · 2009 to 2015
$1.0M
Beta-Catenin in T Cell FunctionZ01AG000772 · NIA · NATIONAL INSTITUTE ON AGING · PI SEN, JYOTI · 2008 to 2008
$224k
Intramural NIH HHS Z01 AG000772
6 · The paper itself

Abstract

The differentiation of activated CD4(+) T cells into the T helper type 1 (T(H)1) or T(H)2 fate is regulated by cytokines and the transcription factors T-bet and GATA-3. Whereas interleukin 12 (IL-12) produced by antigen-presenting cells initiates the T(H)1 fate, signals that initiate the T(H)2 fate are not completely characterized. Here we show that early GATA-3 expression, required for T(H)2 differentiation, was induced by T cell factor 1 (TCF-1) and its cofactor beta-catenin, mainly from the proximal Gata3 promoter upstream of exon 1b. This activity was induced after T cell antigen receptor (TCR) stimulation and was independent of IL-4 receptor signaling through the transcription factor STAT6. Furthermore, TCF-1 blocked T(H)1 fate by negatively regulating interferon-gamma (IFN-gamma) expression independently of beta-catenin. Thus, TCF-1 initiates T(H)2 differentiation of activated CD4(+) T cells by promoting GATA-3 expression and suppressing IFN-gamma expression.

Indexed as

Animalsbeta CateninCell DifferentiationGATA3 Transcription FactorInterferon-gammaInterleukin-12Interleukin-4MiceMice, Inbred C57BLPromoter Regions, GeneticReceptors, Antigen, T-CellReceptors, NotchT Cell Transcription Factor 1Th2 Cellsbeta CateninGata3 protein, mouseGATA3 Transcription FactorInterferon-gammaInterleukin-12Interleukin-4Receptors, Antigen, T-CellReceptors, NotchT Cell Transcription Factor 1

Identifiers

PMID19648923
PMCPMC2824257
OpenAlexW2007359758

What OpenQuestion holds

Textmetadata
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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.