Evidence map›Paper›PMID 23059426›Full record

ReviewNature reviews. Immunology2012

Master regulators or lineage-specifying? Changing views on CD4+ T cell transcription factors.

Kenneth J Oestreich, Amy S Weinmann

Abstract readReview
In one paragraph

Review in Nature reviews. Immunology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed
–field-weighted citation impact
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

78 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Brachyury controlsDevelopment (Cambridge, England) · 2021
    Article
  16. Droplet-based mRNA sequencing of fixed and permeabilized cells by CLInt-seq allows for antigen-specific TCR cloning.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  17. CD8Frontiers in cellular and infection microbiology · 2021
    Article
  18. Article
  19. Article
  20. RORγt-driven TiScience · 2020
    Article

18 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

2 authors.

Kenneth J OestreichDepartment of Immunology, University of Washington, Box 357650, 1959 NE Pacific Street, Seattle, Washington 98195, USA.
Amy S Weinmann

Funding

Molecular characterization of the role for T-bet and Bcl-6 in immune cell metabolism and differentiationR01AI061061 · NIAID · UNIVERSITY OF WASHINGTON · PI WEINMANN, AMY SUSAN · 2004 to 2025
$7.0M
VIRUS INFECTIONS: PATHOGENESIS &HOST IMMUNE RESPONSEST32AI007272 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI FINBERG, ROBERT WILLIAM · 1985 to 2009
$1.9M
Molecular characterization of the role for metabolites in immune cell differentiationR56AI061061 · NIAID · UNIVERSITY OF WASHINGTON · PI WEINMANN, AMY SUSAN · 2009 to 2021
$672k
NIAID NIH HHS AI061061NIAID NIH HHS AI07272NIAID NIH HHS R01 AI061061NIAID NIH HHS R56 AI061061NIAID NIH HHS T32 AI007272
6 · The paper itself

Abstract

There is an emerging body of research demonstrating that the co-expression of key lineage-specifying transcription factors, commonly referred to as 'master regulators', affects the functional capabilities and flexibility of CD4(+) T cell subsets. Here, we discuss how the natural co-expression of these lineage-specifying transcription factors has challenged the concept that the expression of a single 'master regulator' strictly establishes an absolute CD4(+) T cell phenotype. Instead, it is becoming clear that the interplay between the lineage-specifying (or lineage-defining) transcription factors, including T-bet, GATA3, RORγt, BCL-6 and FOXP3, contributes to the fate and flexibility of CD4(+) T cell subtypes. This in turn has led to the realization that CD4(+) T cell phenotypes are more diverse than previously recognized.

Indexed as

CD4-Positive T-LymphocytesCell LineageDNA-Binding ProteinsForkhead Transcription FactorsGATA3 Transcription FactorHumansNuclear Receptor Subfamily 1, Group F, Member 3PhenotypeProto-Oncogene Proteins c-bcl-6T-bet Transcription FactorT-Box Domain ProteinsTranscription FactorsBCL6 protein, humanDNA-Binding ProteinsForkhead Transcription FactorsFOXP3 protein, humanGATA3 protein, humanGATA3 Transcription FactorNuclear Receptor Subfamily 1, Group F, Member 3Proto-Oncogene Proteins c-bcl-6T-bet Transcription FactorT-Box Domain ProteinsTranscription Factors

Identifiers

PMID23059426
PMCPMC3584691

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.