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. 2020 Sep 2;11:1842. doi: 10.3389/fimmu.2020.01842

Table 1.

Immunosuppressive mechanisms employed by MDSCs and TAMs, as well as stereotypic programming that regulate the mechanisms.

Effect Tumor type References
Immunosuppressive mechanism
PD-1/PD-L1 T-cell exhaustion/suppression Myeloid cell suppressive programming Glioma, Breast, Lung (non-small cell) (45, 55, 5861) (108, 109)
CTLA-4/CD80/86 T-cell exhaustion Breast, Lung (45, 58, 110, 111)
B7-H3 Receptor/B7-H3 T-cell exhaustion/suppression Breast, Lung (206, 207)
ARG Environmental nutrient depletion Breast, Lung (45, 62, 63)
IDO Environmental nutrient depletion Breast, Lung (55)
NOS T-cell suppression Breast, Brain, Lung (12, 23, 45, 55, 62, 68, 69)
ROS T-cell suppression Breast, Brain, Lung (12, 55)
Immunosuppressive program
STAT Inhibition of intracellular inflammation cascade in suppressive myeloid cells Anti-apoptosis in suppressive myeloid cells Breast, Brain (GBM), Lung (7578, 81, 82) (27, 79, 80)
PPARγ Inhibition of intracellular inflammation cascade in suppressive myeloid cells Metabolic reprogramming in suppressive myeloid cells Lung, Breast (74, 75) (83)