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"Host Immune and Malignant Cells" collectively refers to the diverse populations of immune cells and cancer cells residing within or recruited to the tumor microenvironment. Their interactions play a central role in cancer initiation, progression, and response to therapy. The immune system can either suppress or promote tumor growth, depending on the balance between anti-tumor immune responses (e.g., cytotoxic T cell activity, macrophage M1 polarization) and pro-tumor/tolerogenic mechanisms (e.g., MDSC accumulation, regulatory T cell induction, M2 macrophage activity, immune checkpoint upregulation such as PD-1/PD-L1 and CTLA-4)[1][2][3][5][6][7]. This dynamic interplay forms the basis for several therapeutic strategies, notably immunotherapies, but it is much too broad and variable to constitute a single molecular target.
Modulation of immune surveillance and response (immune activation or suppression); Blockade of immunosuppressive checkpoints (PD-1/PD-L1, CTLA-4 inhibitors); Induction of immune-mediated tumor cell killing; Immunosuppression or promotion of immunogenicity
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