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. 2022 Jan 8;13(1):1717–1735. doi: 10.1080/21655979.2021.2019873

Table 2.

The effects of high PR risk score on TIM

Immune cell Changing trend Basic function Final effect on antitumor immune
T cells CD8 Decreased CD8 + T cells clear tumor cells through perforin-granzyme and Fas-Fasl pathways. Unfavorable
NK cells Decreased NK cells can kill multiple adjacent cells if these carry with oncogenic markers. Unfavorable
Tregs Increased Tregs actively participate in the maintenance of immunological self-tolerance, thereby inducing cancer immune escape. Unfavorable
Macrophages M0 Increased TAMs can enhance tumor cell invasion and metastasis through secreting VEGF, CCL2, CXCL12, and EGF cytokines. Unfavorable
Macrophages M1 Increased M1 macrophages can mediate the differentiation of T cells and facilitate their immune functions through releasing IL-12 and IL-23. Beneficial
Macrophages M2 Increased M2 macrophages are the majority of TAMs, possessing immunosuppressive capacity and leading poor prognosis. Unfavorable

PR, pyroptosis-related; TIM, tumor immune microenvironment; Tregs, regulatory T cells; TAMs, tumor-associated macrophages; VEGF, vascular endothelial growth factor; CCL2, C-C motif chemokine ligand 2; CXCL12, C-X-C motif chemokine ligand 12; EGF, epidermal growth factor.