Correspondingly, TAMs isolated from phenelzine-treated mice displayed a less immunosuppressive phenotype, evidenced by their decreased expression of immunosuppressive markers (i.e., CD206; Fig. 5i) and signature genes (i.e., Chi3l3 and Arg1; Supplementary Fig. 5c) while increased expression of immunostimulatory markers (i.e., CD69, CD86 and I-Ab; Supplementary Fig. 5d–f), that was correlated with an enhanced antitumor reactivity of tumor-infiltrating CD8+ T cells (i.e., increased production of Granzyme B; Fig. 5j) in these mice. Here, CD69 is linked to neoplasm.