From: The roles of exosomal immune checkpoint proteins in tumors
Origin of exosomes | Immune checkpoint proteins carried by exosomes | Targeted cells | Effect | References |
---|---|---|---|---|
PC3, prostate cancer cell lines | PD-L1 | Jurkat T cells | Suppress Jurkat T cells activation | [51] |
TRAMP-C2, human prostate cancer-like cells | PD-L1 | CD4+/CD8+ T cells | Suppress CD4+ and CD8+ T cells activation | [51] |
Glioblastoma cells | PD-L1 | CD4+ T cells, CD8+ T cells | Suppress T cell activation and proliferation | [56] |
ESCC cells | PD-L1 | B cells, Breg cells | Inhibit the proliferation of B cells; induce an increase in B10 and PD-1high Breg cells; activate TLR4 and MAPK signaling pathways | [54] |
Breast cancer cells | PD-L1 | CTLs | Promote tumor growth | [55] |
HNSCC cells | PD-L1 | CD8+ T cells | Suppress T cell activation | [52] |
Metastatic melanoma cells | PD-L1 | CD8+ T cells | Suppress the function of CD8+ T cells; facilitate tumor growth | [57] |
MEL624 cells, human melanoma cell lines | PD-L1 | CD8+ T cells | Inhibit the proliferation, cytokine production and cytotoxicity of CD8+ T cells; reduce expression of Ki-67 and GzmB, inhibit the production of IFN-γ, IL-2, and TNF-α | [57] |
B16-F10 cells, mouse melanoma cell lines | PD-L1 | CD8+ T cells | Inhibit the proliferation and cytotoxicity of mouse splenic CD8+ T cells | [57] |
Glioblastoma cells | CTLA-4 | CD4+ T cells, CD8+ T cells, NK cells, macrophages | Inhibit the immune cell function | [48] |
NSCLC cells | TIM-3 | – | Positively correlate with larger tumor size, advanced stages and more distant metastasis | [49] |
Epithelial OvCa cells | ARG1 | CD4+ T cells, CD8+ T cells | Inhibit the proliferation of antigen-specific T cells; accelerate tumor progression | [43] |
ID8-ARG1-V5 cells | ARG1 | BMDCs | Inhibit CD8+ and CD4+ T cells proliferation | [43] |
Prostate cancer cells | EBAG9 | CTLs | Inhibit the cytotoxicity of T cells; negatively regulate tumor surveillance in host cells | [39] |