Evidence map›Paper›PMID 24951034›Full record

ReviewTrends in immunology2014

Fine-tuning T cell receptor signaling to control T cell development.

Guo Fu, Vasily Rybakin, Joanna Brzostek, Wolfgang Paster, Oreste Acuto, Nicholas R J Gascoigne

Abstract readReview
In one paragraph

Review in Trends in immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing 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

44 citing papers in PubMed.

  1. Article
  2. Review
  3. Food for thought: Nutrient metabolism controlling early T cell development.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  4. Review
  5. Article
  6. TCR Signals Controlling Adaptive Immunity against Toxoplasma and Cancer.Advances in experimental medicine and biology · 2024
    Article
  7. The Function of Ubiquitination in T-Cell Development.Advances in experimental medicine and biology · 2024
    Review
  8. Article
  9. Article
  10. Themis suppresses the effector function of CD8Cellular & molecular immunology · 2023
    Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  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

6 authors.

Guo FuDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037, USA.
Vasily RybakinDepartment of Microbiology, Yong Loo Lin School of Medicine, National University of Singapore, 5 Science Drive 2, Singapore 117597.
Joanna BrzostekDepartment of Microbiology, Yong Loo Lin School of Medicine, National University of Singapore, 5 Science Drive 2, Singapore 117597.
Wolfgang PasterSir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.
Oreste AcutoSir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.
Nicholas R J GascoigneDepartment of Microbiology, Yong Loo Lin School of Medicine, National University of Singapore, 5 Science Drive 2, Singapore 117597. Electronic address: micnrjg@nus.edu.sg.

Funding

Intermolecular Interactions in the Immunological SynapseR01GM065230 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI SAUER, KARSTEN · 2002 to 2014
$4.6M
Themis in Type II DiabetesR21DK094173 · NIDDK · SCRIPPS RESEARCH INSTITUTE, THE · PI GASCOIGNE, NICHOLAS R · 2012 to 2013
$513k
NIDDK NIH HHS DK094173NIDDK NIH HHS R21 DK094173NIGMS NIH HHS GM065230NIGMS NIH HHS R01 GM065230Wellcome TrustWellcome Trust WT094296MA
6 · The paper itself

Abstract

T cell development from immature CD4(+)CD8(+) double-positive (DP) thymocytes to the mature CD4 or CD8 single-positive (SP) stage requires proper T cell receptor (TCR) signaling. The current working model of thymocyte development is that the strength of the TCR-mediated signal - from little-or-none, through intermediate, to strong - received by the immature cells determines whether they will undergo death by neglect, positive selection, or negative selection, respectively. In recent years, several developmentally regulated, stage-specifically expressed proteins and miRNAs have been found that act like fine-tuners for signal transduction and propagation downstream of the TCR. This allows them to govern thymocyte positive selection. Here, we summarize recent findings on these molecules and suggest new concepts of TCR positive-selection signaling.

Indexed as

AnimalsCalcium SignalingCell DifferentiationClonal Selection, Antigen-MediatedFetal ProteinsHumansIntracellular Signaling Peptides and ProteinsMicroRNAsProtein Tyrosine Phosphatase, Non-Receptor Type 6Receptor Cross-TalkReceptors, Antigen, T-CellThymocytesT-LymphocytesFetal ProteinsIntracellular Signaling Peptides and ProteinsMicroRNAsProtein Tyrosine Phosphatase, Non-Receptor Type 6Receptors, Antigen, T-Cellthymocyte-expressed molecule involved in selection, humanmiR-181signalingT cell developmentTespa1Themisthymocytevoltage-gated sodium channel

Identifiers

PMID24951034
PMCPMC4119814

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.