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The immune microenvironment refers to the dynamic, context-dependent community of immune cells (such as T cells, B cells, macrophages, dendritic cells, myeloid-derived suppressor cells), soluble mediators (cytokines, chemokines), and stromal elements surrounding tissues (commonly, tumors). Its composition and function can promote effective immune surveillance against abnormal cells (tumor or infected), but may also become dysregulated, contributing to immune escape, chronic inflammation, or tissue damage. In cancer, the tumor immune microenvironment profoundly influences tumor progression, immune evasion, therapy response, and the effectiveness of immunotherapies.
Modulation of immune checkpoints (restoring T cell activity, e.g., PD-1/PD-L1 blockade); Depletion or reprogramming of suppressive immune cells (e.g., targeting Tregs, MDSCs); Recruitment/activation of effector immune cells (e.g., CAR-T cells); Inhibiting pro-tumor cytokine/chemokine signaling; Enhancing antigen presentation and immune priming. These mechanisms act via cellular interactions and signal-modulation within the immune microenvironment.
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