Extracellular vesicle PD-L1 in reshaping tumor immune microenvironment: biological function and potential therapy strategies

被引:38
作者
Liu, Jiaxing [1 ]
Peng, Xueqiang [1 ]
Yang, Shuo [1 ]
Li, Xinyu [1 ]
Huang, Mingyao [1 ]
Wei, Shibo [1 ]
Zhang, Sheng [1 ]
He, Guangpeng [1 ]
Zheng, Hongyu [1 ]
Fan, Qing [1 ]
Yang, Liang [1 ]
Li, Hangyu [1 ]
机构
[1] China Med Univ, Dept Gen Surg, Affiliated Hosp 4, Shenyang 110032, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
PD-L1; Extracellular vesicles; Immune escape; Biomarker; Immunotherapy; LIGAND; 1; EXPRESSION; SIGNALING PATHWAYS; ANTITUMOR IMMUNITY; REGULATING PD-L1; SHEDDING LIGHT; EMERGING ROLE; CANCER CELLS; IFN-GAMMA; EXOSOMES; MICROVESICLES;
D O I
10.1186/s12964-021-00816-w
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Programmed cell death 1 ligand 1 (PD-L1) is the ligand for programmed death protein-1 (PD-1), is associated with immunosuppression. Signaling via PD-1/PD-L1 will transmits negative regulatory signals to T cells, inducing T-cell inhibition, reducing CD8(+) T-cell proliferation, or promoting T-cell apoptosis, which effectively reduces the immune response and leads to large-scale tumor growth. Accordingly, many antibody preparations targeting PD-1 or PD-L1 have been designed to block the binding of these two proteins and restore T-cell proliferation and cytotoxicity of T cells. However, these drugs are ineffective in clinical practice. Recently, numerous of studies have shown that, in addition to the surface of tumor cells, PD-L1 is also found on the surface of extracellular vesicles secreted by these cells. Extracellular vesicle PD-L1 can also interact with PD-1 on the surface of T cells, leading to immunosuppression, and has been proposed as a potential mechanism underlying PD-1/PD-L1-targeted drug resistance. Therefore, it is important to explore the production, regulation and tumor immunosuppression of PD-L1 on the surface of tumor cells and extracellular vesicles, as well as the potential clinical application of extracellular vesicle PD-L1 as tumor biomarkers and therapeutic targets.
引用
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页数:18
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