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Activating receptors on cytokine-induced killer cells comprise a group of surface molecules, most notably NKG2D, DNAM-1, and NKp30, that enable CIK cells to recognize and destroy malignant or infected cells independent of classical MHC pathways. These receptors are essential for the non-specific, rapid cytotoxic function of CIK cells, rendering them effective in tumor immunotherapy and some infectious diseases. They interact with stress-induced ligands overexpressed on diseased but not healthy cells and facilitate immune activation, cell signaling, and target cell lysis. Targeting these receptors with cell therapies or enhancing their activity is a promising strategy in cancer treatment, though safety and specificity must be carefully managed.
Drug/cell therapy products that activate, upregulate, or co-stimulate these receptors (e.g., through cytokine induction or genetic engineering) enhance CIK cell antitumor or antiviral activity.
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