Tissue-resident memory CD8+ T cells in cancer immunology and immunotherapy.

Abstract:

:Memory T cells can be generated and remain long-term in different tissues following infection or immunization. Tissue-resident memory T (TRM) cells are a unique group of memory T cells that form and persist mainly in peripheral non-lymphoid organs. Unlike effector or central memory T (TEM or TCM) cells, TRM cells do not circulate to the blood but can provide a rapid and robust local response to re-infection. Recently, a large body of clinical studies has shown that CD103+ CD8+ TRM-like cells also exist intratumorally and strongly correlate with favorable prognosis in cancer patients. Cancer vaccine-induced CD103+ CD8+ TRM cells have been reported to suppress tumor growth in mouse models. This suggests that CD8+ TRM-like cells play a crucial role in cancer immunosurveillance and immunotherapy. In this review, we focus on the features and cytotoxic mechanisms of CD8+ TRM-like cells in multiple solid tumors and discuss their potential implications for cancer immunotherapy. We believe a better understanding of the generation, function, and longevity of CD8+ TRM-like cells in the tumor microenvironment will provide new insights for cancer immunotherapies.

journal_name

Pharmacol Res

journal_title

Pharmacological research

authors

Wang T,Shen Y,Luyten S,Yang Y,Jiang X

doi

10.1016/j.phrs.2020.104876

subject

Has Abstract

pub_date

2020-09-01 00:00:00

pages

104876

eissn

1043-6618

issn

1096-1186

pii

S1043-6618(20)31184-1

journal_volume

159

pub_type

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