High expression of miR—203 |
Dendritic cells |
Down-regulation of TLR4 and downstream cytokines, thereby inhibiting the immune response |
[57] |
High expression of miR-212-3p |
Dendritic cells |
Inhibit the expression of regulatory factor X-associated protein (RFXAP), reduce the expression of MHC II, and produce immune tolerance |
[58] |
High expression of CD63 |
T lymphocyte |
Activate p38 mitogen-activated protein kinase (MAPK), induce cell apoptosis, and eventually lead to immunosuppression |
[56] |
High expression of tumor-associated antigens (TAAs) |
B cell |
As a bait for complement, it produces cytotoxicity and inhibits specific immune response |
[60] |
High expression of macrophage migration inhibitory factor (MIF) |
Bone marrow-derived macrophages |
Immunosuppressive cells are recruited to form an immunosuppressive environment |
[40] |
High expression of miR153 |
NK cells |
Natural killer group 2 member D (NKG2D) was reduced by upregulation of hypoxia inducible factor 1-α (Hi1FA), and NK cells cleavage |
[79] |
High expression of miR-338-3p |
Neutrophils |
At present, the mechanism of action is not clear, biochemistry analysis indicated that it can inhibit the function of immune cells |
[80] |
High expression of miR-199b-5p |
Neutrophils |
At present, the mechanism of action is not clear, biochemistry analysis indicated that it can inhibit the function of immune cells |
[80] |
Lower expression of miR-340 |
Macrophages |
At present, the mechanism of action is not clear, inhibits macrophages from becoming M1-like phenotype polarization in the peripheral and tumor immune microenvironment, and reduces T cells, especially CD8 + T cells |
[81] |
Lower expression of miR-128 |
All kinds of immune cells |
At present, the mechanism of action is not clear, biochemistry analysis indicated that it can inhibit the function of immune cells |
[64] |