TIGIT+ TIM-3+ NK cells are correlated with NK cell exhaustion and disease progression in patients with hepatitis B virus-related hepatocellular carcinoma

被引:57
作者
Yu, Lihua [1 ]
Liu, Xiaoli [1 ]
Wang, Xinhui [1 ]
Yan, Fengna [1 ]
Wang, Peng [1 ]
Jiang, Yuyong [1 ]
Du, Juan [2 ]
Yang, Zhiyun [1 ]
机构
[1] Capital Med Univ, Beijing Ditan Hosp, Ctr Integrat Med, Beijing 100015, Peoples R China
[2] Capital Med Univ, Beijing Ditan Hosp, Inst Infect Dis, Beijing Key Lab Emerging Infect Dis, Beijing 100015, Peoples R China
来源
ONCOIMMUNOLOGY | 2021年 / 10卷 / 01期
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
Hepatocellular carcinoma; Natural killer cells; TIGIT; TIM-3; co-expression; FUNCTIONAL IMPAIRMENT; ADVANCED MELANOMA; T-CELLS; EXPRESSION; CYTOTOXICITY; REVERSAL;
D O I
10.1080/2162402X.2021.1942673
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The prognosis of hepatocellular carcinoma (HCC) is extremely poor, of which hepatitis B virus-related hepatocellular carcinoma (HBV-HCC) accounts for the majority in China. Immune checkpoint inhibitors have become an effective immunotherapy method for the treatment of HCC, but they are mainly used for T cells. NK cells play a vital role as the first line of defense against tumors. Therefore, we explored the characteristic expression pattern of immune checkpoints on NK cells of HBV-HCC patients. We analyzed the correlation between the co-expression of TIGIT and TIM-3 and the clinical progress of patients with HBV-HCC. The co-expression of TIGIT and TIM-3 on NK cells is elevated in patients with HBV-HCC. TIGIT(+)TIM-3(+)NK cells showed exhausted phenotypic characteristics and displayed dysfunction manifested as weakened killing function, reduced cytokine production, and proliferation function. TIGIT(+)TIM-3(+)NK cells participate in NK cells function exhaustion and are closely related to the disease progression of patients with HBV-HCC, suggesting a new target for future immunotherapy.
引用
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页数:13
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