14
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Activation of V gamma 9V delta 2 T cells by NKG2D.

      The Journal of Immunology Author Choice
      Animals, Antibodies, Monoclonal, metabolism, Biological Markers, blood, CD8-Positive T-Lymphocytes, immunology, secretion, Cell Line, Cell Line, Tumor, Cells, Cultured, Cytokines, biosynthesis, Cytoplasmic Granules, Cytotoxicity Tests, Immunologic, Histocompatibility Antigens Class I, physiology, Humans, Killer Cells, Natural, Ligands, Lymphocyte Activation, Membrane Proteins, Mice, NK Cell Lectin-Like Receptor Subfamily K, Receptors, Antigen, T-Cell, gamma-delta, Receptors, Immunologic, Receptors, Natural Killer Cell, T-Lymphocyte Subsets

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Human Vgamma9 Vdelta2 T cells recognize phosphorylated nonpeptide Ags (so called phosphoantigens), certain tumor cells, and cells treated with aminobisphosphonates. NKG2D, an activating receptor for NK cells, has been described as a potent costimulatory receptor in the Ag-specific activation of gammadelta and CD8 T cells. This study provides evidence that Vgamma9 Vdelta2 T cells may also be directly activated by NKG2D. Culture of PBMC with immobilized NKG2D-specific mAb or NKG2D ligand MHC class I related protein A (MICA) induces the up-regulation of CD69 and CD25 in NK and Vgamma9 Vdelta2 but not in CD8 T cells. Furthermore, NKG2D triggers the production of TNF-alpha but not of IFN-gamma, as well as the release of cytolytic granules by Vgamma9 Vdelta2 T cells. Purified Vgamma9 Vdelta2 T cells kill MICA-transfected RMA mouse cells but not control cells. Finally, DAP10, which mediates NKG2D signaling in human NK cells, was detected in resting and activated Vgamma9 Vdelta2 T cells. These remarkable similarities in NKG2D function in NK and Vgamma9 Vdelta2 T cells may open new perspectives for Vgamma9 Vdelta2 T cell-based immunotherapy, e.g., by Ag-independent killing of NKG2D ligand-expressing tumors.

          Related collections

          Author and article information

          Comments

          Comment on this article