Evidence map›Paper›PMID 18990450›Full record

ArticleMolecular immunology2009

IL-2 signaling prevents T cell anergy by inhibiting the expression of anergy-inducing genes.

Myrianne Duré, Fernando Macian

Open access · greenAbstract read
In one paragraph

Article in Molecular immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

34 citing papers in PubMed, 62 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. CD8Frontiers in immunology · 2022
    Review
  7. Article
  8. Genome-Wide miRNA Expression Profiling of Molecular Subgroups of Peripheral T-cell Lymphoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Article
  9. Article
  10. Article
  11. Review
  12. Dimethyl fumarate as a first- vs second-line therapy in MS: Focus on B cells.Neurology(R) neuroimmunology & neuroinflammation · 2018
    Article
  13. Article
  14. Drug-perturbation-based stratification of blood cancer.The Journal of clinical investigation · 2018
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Review
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 at 1 institution in 1 country.

Myrianne DuréDepartment of Pathology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.
Fernando Macian
Albert Einstein College of Medicine · US

Funding

Molecular mechanisms of T cell anergyR01AI059738 · NIAID · ALBERT EINSTEIN COL OF MED YESHIVA UNIV · PI MACIAN, FERNANDO · 2004 to 2014
$3.9M
Molecular mechanisms of T cell anergyR56AI059738 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI MACIAN, FERNANDO · 2016 to 2016
$418k
NIAID NIH HHS AI059738NIAID NIH HHS R01 AI059738NIAID NIH HHS R56 AI059738
6 · The paper itself

Abstract

T cell responses are determined by the environment in which antigen is encountered. In the absence of proper costimulation, anergizing stimuli induce the activation of a specific program of gene expression. Proteins encoded by these genes impose a state of functional unresponsiveness in anergic T cells through the activation of different mechanisms that include dampening of the T cell receptor signaling and direct inhibition of cytokine expression. Anergy can be reversed by stimulating T cells in the presence of interleukin (IL-)2. Signaling through the IL-2 receptor has been shown to activate mTOR, which plays an important role in the integration of signals that determine the fate of T cells. The mechanisms underlying the IL-2-dependent regulation of T cell tolerance are still not fully elucidated. In this study we show that IL-2 receptor signaling mediated through JAK3 and mTOR inhibits the expression of anergy-inducing genes independently of any effect on cell cycle progression. Interestingly, we also show that this effect is likely due to changes on the levels of AP-1 activation induced by IL-2 receptor signaling in T cells. Our data identifies a mechanism that can explain how IL-2 may prevent or reverse the establishment of anergy in T cells and, therefore, helps to understand how the cytokine environment can be determinant to shape the outcome of T cell responses - tolerance or activation - when antigen is encountered.

Indexed as

AnimalsCell CycleClonal AnergyGene Expression RegulationInterleukin-2Janus Kinase 3MiceMice, Inbred BALB CProtein KinasesReceptors, Interleukin-2Signal TransductionT-LymphocytesTOR Serine-Threonine KinasesTranscription Factor AP-1Interleukin-2Jak3 protein, mouseJanus Kinase 3mTOR protein, mouseProtein KinasesReceptors, Interleukin-2TOR Serine-Threonine KinasesTranscription Factor AP-1

Identifiers

PMID18990450
PMCPMC2667138
OpenAlexW2140999266

What OpenQuestion holds

Textmetadata
LicenceTDM
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.