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Myeloid-derived suppressor cells (MDSCs) are a heterogeneous population of immature myeloid cells known for their potent immunosuppressive activity. The expression of NKG2D ligands (NKG2DLs) on MDSCs makes them targets for NK cells and cytotoxic T lymphocytes (CTLs) via the NKG2D receptor. This interaction can lead to both immune activation (killing of MDSCs) and immune suppression (exhaustion of effector cells), depending on the context and the tumor's manipulation of the pathway. Therefore, modulating the NKG2D-NKG2DL axis on MDSCs is being explored as a therapeutic strategy in cancer immunotherapy.
Modulation of NKG2D-NKG2D ligand interaction to enhance or suppress immune responses.
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