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. 2022 Jan 28;20:14. doi: 10.1186/s12964-021-00816-w

Table 2.

The effects of extracellular vesicle PD-L1 on tumor cells

Type of tumor Target cell Effect References
Direct effects
Prostate cancer CD4+/CD8+T cells Inhibition of T-cell activation and activity; the percentage of the depletion marker Tim3 increased, while that of the activation marker granzyme B percentage decreased [9]
Melanoma CD8+T cells Inhibited the proliferation, cytokine production and cytotoxicity of CD8+T cells [8]
Breast cancer T cells Inhibited the indicators of T-cell activation, such as NF-κB activation, as well as PHA-induced interleukin 2 (IL-2) secretion [123]
Head and neck cancer CD8+T cells Inhibited the expression of CD69 (a marker of T-cell activation) [124]
Pancreatic cancer Exo-PD-L1 expression negatively correlated with postoperative survival time in patients with pancreatic ductal adenocarcinoma [125]
Glioblastoma CD4+/CD8+T cells The expression of CD69 and CD25 and proliferative ability in CD4+ and CD8+ T cells decreased [114]
Gastric cancer CD4+/CD8+T cells Inhibition of T-cell proliferation and negative correlation with granzyme B [126]
Non-small cell lung cancer Jurkat cells/CD8+T cells Decreased the production of INF-γ and induced apoptosis [127]
Indirect effects
Glioblastoma Monocytes Extracellular vesicles of gastric cancer cells induce PD-L1 expression on neutrophils to inhibit T-cell-mediated immunity [133]
Gastric cancer Neutrophils EVs of gastric cancer cells induce PD-L1 expression on neutrophils to inhibit T cell immunity [134]
Chronic lymphocytic leukemia Monocytes CLL-derived exosomes increased PD-L1 expression; increased CCL2, CCL4, and IL-6 secretion from monocytes [138]
Liver Cancer Macrophages Hepatoma cells release mir-23a-3p-containing exosomes and upregulate the expression of PD-L1 in macrophages, thereby reducing the ratio of CD8+ T cells and promoting T-cell apoptosis [139]
Non-small cell lung cancer Macrophages Exosomes derived from non-small cell lung cancer cells promote the expression of PD-L1 on the surface of macrophages, and then inhibit tumor immunity [137]