1. Cytokine-driven regulation of NK cell functions in tumor immunity: role of the MICA-NKG2D system.
- Author
-
Zwirner NW, Fuertes MB, Girart MV, Domaica CI, and Rossi LE
- Subjects
- Animals, Cell Communication immunology, Dendritic Cells immunology, Dendritic Cells pathology, Humans, Killer Cells, Natural pathology, NK Cell Lectin-Like Receptor Subfamily K, Neoplasms pathology, Receptors, Natural Killer Cell, Th1 Cells immunology, Th1 Cells pathology, Histocompatibility Antigens Class I immunology, Killer Cells, Natural immunology, Neoplasms immunology, Receptors, Immunologic immunology, Tumor Escape
- Abstract
Natural killer (NK) cells are critical players during tumor growth control in immunocompetent hosts. These cells also establish a cross-talk with dendritic cells (DCs) and promote a Th1-mediated immunity. NKG2D is a pivotal receptor that directs the tumoricidal activity of NK cells through the recognition of a group of ligands such as MICA widely expressed on different tumors. Here we will review the most important tumor immune escape mechanisms that compromise the functionality of NKG2D and its cognate ligands, including TGF-beta secretion, tumor shedding of soluble MICA, and additional mechanisms that compromise the tumoricidal activity of NKG2D-expressing cells. Such mechanisms may also dampen the cross-talk between NK cells and DCs during the anti-tumor immune responses. Recent knowledge may lead to innovative approaches to promote efficient NK cell-mediated anti-tumor immune responses.
- Published
- 2007
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