Costimulation of CD8αβ T cells by NKG2D via engagement by MIC induced on virus-infected cells
By V. Groh, R. Rhinehart, J. Randolph-Habecker, M. Topp, S. Riddell, T. Spies. Nature Immunology, 2001
723 citations recorded by the source corpus.
Subfields: Epidemiology, Immunology
View Paper: https://www.semanticscholar.org/paper/fab0567ce17a5e37bce95a36e6a3606a9d368ed3
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Citations in the corpus
- Regulation of ligands for the NKG2D activating receptor (2013, background): “In conventional CD8+ T cells, NKG2D may also provide costimulatory function (16, 17), although this is most evident for the subset of highly activated CD8+ T cells that lacks expression of CD28, the conventional costimulatory receptor for T cells (16).”
- Natural killer cells, viruses and cancer (2001, background): “A role for NKG2D in the co-stimulation of CD8+ T cells during HCMV recognition was recently shown by Groh et al.66.”
- The role of the NKG2D immunoreceptor in immune cell activation and natural killing. (2002, neutral): “(Groh et al., 2001).”
- Cutting Edge: Down-Regulation of MICA on Human Tumors by Proteolytic Shedding (2002, background): “Engagement of NKG2D by MICA expressed on transfectants and tumor cell lines triggers NK cells and V 1 T cells and costimulates CD8 T cells (4, 8, 9).”