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Cited by 673

The DOI matches its Crossref record; 19 of the 19 references it cites were found in a registry or an index.

Tolerance and exhaustion: defining mechanisms of T cell dysfunction

Open access
Schietinger, Andrea, Greenberg, Philip D.·2014·Trends in Immunology

Abstract

CD8 T cell activation and differentiation is 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 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.

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Metadata

Authors
Schietinger, A., & Greenberg, P. D.
Venue
Trends in Immunology
Publisher
Elsevier BV
Published
2014-02
Volume
35
Issue
2
Pages
51-60
ISSN
1471-4906 (ISSN-L)
OpenAlex
W2023003954
Cited by
673
References
19
FWCI
1.80
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Tolerance and exhaustion: defining mechanisms of T cell dysfunction. https://app.cochat.ai/papers/10.1016/j.it.2013.10.001
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Schietinger, A., & Greenberg, P. D. (2014). Tolerance and exhaustion: defining mechanisms of T cell dysfunction. Trends in Immunology. https://doi.org/10.1016/j.it.2013.10.001

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.