Evidence map›Paper›PMID 24210163›Full record

ReviewTrends in immunology2014

Tolerance and exhaustion: defining mechanisms of T cell dysfunction.

Andrea Schietinger, Philip D Greenberg

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 433 papers.

0numbers the graph read from it
0cells of the map it votes in
433citing 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

433 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Interferon regulatory factors orchestrate CD8International journal of molecular medicine · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. HBV-driven expansion of CXCR6Innovation (Cambridge (Mass.)) · 2026
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Post-Translational Regulation of CD8Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  19. Article
  20. Article

373 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.

Andrea SchietingerDepartment of Immunology, University of Washington, Seattle, WA 98109, USA; Program of Immunology, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA. Electronic address: aschieti@uw.edu.
Philip D GreenbergDepartment of Immunology, University of Washington, Seattle, WA 98109, USA; Program of Immunology, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA. Electronic address: pgreen@u.washington.edu.

Funding

VIRUS-MEDIATED MYELOSUPPRESSIONP01CA018029 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Ted A Gooley · 1985 to 2026
$128.4M
Mechanisms of Murine Turmor Eradication by ImmunotherapyR01CA033084 · NCI · UNIVERSITY OF WASHINGTON · PI GREENBERG, PHILIP D · 1986 to 2017
$5.8M
Chromatin states encoding fate commitment and plasticity of tolerant CD8 T cellsR21AI107776 · NIAID · UNIVERSITY OF WASHINGTON · PI GREENBERG, PHILIP D · 2013 to 2014
$413k
Molecular and Epigenetic Programs Underlying T cell Tolerance to Tumor AntigensK99CA172371 · NCI · UNIVERSITY OF WASHINGTON · PI SCHIETINGER, ANDREA · 2013 to 2014
$340k
NCI NIH HHS K99 CA172371NCI NIH HHS P01 CA018029NCI NIH HHS R01 CA033084NIAID NIH HHS R21 AI107776
6 · The paper itself

Abstract

CD8 T cell activation and differentiation are tightly controlled, and dependent on the context in which naïve T cells encounter antigen, can either result in functional memory or T cell dysfunction, including exhaustion, tolerance, anergy, or senescence. With the identification of phenotypic and functional traits shared in different settings of T cell dysfunction, distinctions between such dysfunctional states have become blurred. Here, we discuss distinct states of CD8 T cell dysfunction, with an emphasis on: (i) T cell tolerance to self-antigens (self-tolerance); (ii) T cell exhaustion during chronic infections; and (iii) tumor-induced T cell dysfunction. We highlight recent findings on cellular and molecular characteristics defining these states, cell-intrinsic regulatory mechanisms that induce and maintain them, and strategies that can lead to their reversal.

Indexed as

Immune ToleranceAnimalsCD8-Positive T-LymphocytesCell DifferentiationClonal AnergyEpigenesis, GeneticHumansImmunologic MemoryInfectionsLymphocyte ActivationMiceNeoplasmsSelf ToleranceCD8 T cellschronic infectionexhaustionself-toleranceT cell differentiationT cell dysfunctiontumors

Identifiers

PMID24210163
PMCPMC3946600

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.