Exhausted T cells in tumors gain suppressor activity and can restrain immunity
- PMID: 36650281
- DOI: 10.1038/s41590-022-01409-6
Exhausted T cells in tumors gain suppressor activity and can restrain immunity
Comment on
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Hypoxia drives CD39-dependent suppressor function in exhausted T cells to limit antitumor immunity.Nat Immunol. 2023 Feb;24(2):267-279. doi: 10.1038/s41590-022-01379-9. Epub 2022 Dec 21. Nat Immunol. 2023. PMID: 36543958 Free PMC article.
References
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- Wang, H., Franco, F. & Ho, P. C. Metabolic regulation of Tregs in cancer: opportunities for immunotherapy. Trends Cancer 3, 583–592 (2017). A review article that describes the effects of Treg cell infiltration in cancer and therapeutic strategies to subvert them.
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- Blank, C. U. et al. Defining ‘T cell exhaustion’. Nat. Rev. Immunol. 19, 665–674 (2019). A review article presenting our understanding of the generation and maintenance of T cell exhaustion. - DOI
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- Miller, B. C. et al. Subsets of exhausted CD8+ T cells differentially mediate tumor control and respond to checkpoint blockade. Nat. Immunol. 20, 326–336 (2019). This paper identifies a subset of exhausted T cells responsive to PD-1 blockade.
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- Canale, F. P. et al. CD39 expression defines cell exhaustion in tumor-infiltrating CD8+ T cells. Cancer Res. 78, 115–128 (2018). This paper reports CD39 as a key defining marker of terminally exhausted T cells.
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- Scharping, N. E. et al. Mitochondrial stress induced by continuous stimulation under hypoxia rapidly drives T cell exhaustion. Nat. Immunol. 22, 205–215 (2021). This paper defines a key role for hypoxia in accelerating T cell exhaustion. - DOI
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