4-1BB Delineates Distinct Activation Status of Exhausted Tumor-Infiltrating CD8(+) T Cells in Hepatocellular Carcinoma

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Background and Aims Targeting costimulatory receptors with agonistic antibodies is a promising cancer immunotherapy option. We aimed to investigate costimulatory receptor expression, particularly 4-1BB (CD137 or tumor necrosis factor receptor superfamily member 9), on tumor-infiltrating CD8(+) T cells (CD8(+) tumor-infiltrating lymphocytes [TILs]) and its association with distinct T-cell activation features among exhausted CD8(+) TILs in hepatocellular carcinoma (HCC). Approach and Results Tumor tissues, adjacent nontumor tissues, and peripheral blood were collected from HCC patients undergoing surgical resection (n = 79). Lymphocytes were isolated and used for multicolor flow cytometry, RNA-sequencing, and in vitro functional restoration assays. Among the examined costimulatory receptors, 4-1BB was most prominently expressed on CD8(+) TILs. 4-1BB expression was almost exclusively detected on CD8(+) T cells in the tumor-especially on programmed death 1 (PD-1)(high) cells and not PD-1(int) and PD-1(neg) cells. Compared to PD-1(int) and 4-1BB(neg)PD-1(high) CD8(+) TILs, 4-1BB(pos)PD-1(high) CD8(+) TILs exhibited higher levels of tumor reactivity and T-cell activation markers and significant enrichment for T-cell activation gene signatures. Per-patient analysis revealed positive correlations between percentages of 4-1BB(pos) cells among CD8(+) TILs and levels of parameters of tumor reactivity and T-cell activation. Among highly exhausted PD-1(high) CD8(+) TILs, 4-1BB(pos) cells harbored higher proportions of cells with proliferative and reinvigoration potential. Our 4-1BB-related gene signature predicted survival outcomes of HCC patients in the The Cancer Genome Atlas cohort. 4-1BB agonistic antibodies enhanced the function of CD8(+) TILs and further enhanced the anti-PD-1-mediated reinvigoration of CD8(+) TILs, especially in cases showing high levels of T-cell activation. Conclusion 4-1BB expression on CD8(+) TILs represents a distinct activation state among highly exhausted CD8(+) T cells in HCC. 4-1BB costimulation with agonistic antibodies may be a promising strategy for treating HCCs exhibiting prominent T-cell activation.
Publisher
WILEY
Issue Date
2020-03
Language
English
Article Type
Article
Citation

HEPATOLOGY, v.71, no.3, pp.955 - 971

ISSN
0270-9139
DOI
10.1002/hep.30881
URI
http://hdl.handle.net/10203/274721
Appears in Collection
MSE-Journal Papers(저널논문)
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