Table 1.
Elements of the tumor microenvironment of thymic epithelial tumors associated with favorable and dismal prognosis.
Favorable Prognosis |
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High PD-L1 expression on tumor cells (controversial) [11] |
Moderate and high levels of CD3+ TILs (IHC2 or 3 vs IHC1) [11] |
Higher proportion of neutrophils, Th2 cells, TILs, iDCs, CD8+ T cells [31] |
Dismal Prognosis |
High PD-L1 expression on tumor cells (controversial) [16] |
Lower expression level of HMGB1 [9] |
Higher proportion of immune macrophages, NK cells, Treg, Type II IFN response, and aDCs [31] |
High tumor mutational burden [35] |
Tumor-associated macrophages (further investigation is needed) [38,39,40,41,42] |
HSP27 and 70 expression [42,43,44,45,46,47] |
High SOX9 expression [52] |
PD-L1: programmed death ligand 1, TILs: tumor infiltrating lymphocytes, Th2 cells: T helper 2 cells, iDCs: immature dendritic cells, HMGB1: high mobility group box 1, NK cells: natural killer cells, Treg: T regulatory cells, aDCs: activated dendritic cells, HSP27 and 70: Heat Shock Protein 27 and 70, SOX9: SRY-related high-mobility group box 9.