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. 2022 Dec 1;13:1038715. doi: 10.3389/fimmu.2022.1038715

Figure 2.

Figure 2

Schematic presentation of the mechanisms of immune checkpoint inhibitors (ICIs) and regulation of the tumor immune microenvironment (TIME). Tumor cells bind to PD-1 on the surface of T cells by overexpressing PD-L1 or PD-L2 molecules, thus inactivating T cells for immune escape. ICIs can inhibit these interactions by binding to PD-1 or PD-L1 and then activate cytotoxic T cells and other immune cells to kill tumor cells. (A). TIL: Specific immune response to tumor cells. (B) APCs present antigens, stimulate T cells and transmit immune signals. (C) Th1: Mediates the cellular immune response and promotes cytotoxic T-cell (CTL) killing. (D) MDSCs: Inhibit the body immune cells to play normal innate and adaptive immune functions; Treg: Suppress the immune response of other cells and control self-tolerance) (by Figdraw).