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Cutting Edge: NKG2D Is a Costimulatory Receptor for Human Naive CD8+ T Cells
Author(s) -
Kerima Maasho,
Jessica OpokuAnane,
Alina I. Marusina,
John E. Coligan,
Francisco Borrego
Publication year - 2005
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.174.8.4480
Subject(s) - nkg2d , cytotoxic t cell , cd28 , microbiology and biotechnology , cd8 , biology , priming (agriculture) , mhc class i , il 2 receptor , immune system , t cell , immunology , in vitro , biochemistry , botany , germination
In humans, all alpha beta CD8+ T cells express NKG2D, but in mouse, it is only expressed by activated and memory CD8+ T cells. We purified human naive CD8+ T cells to show that NKG2D serves as a costimulatory receptor for TCR induced Ca2+ mobilization and proliferation. The resulting effector cells are skewed toward a type 1 phenotype and produce high levels of IFN-gamma and TNF-alpha. NKG2D ligands, MHC class I chain-related (MIC)A, MICB, and UL16-binding proteins are expressed on the proliferating cells and NKG2D is down-regulated. The addition of the homeostatic cytokines IL-7 and IL-15 to the culture medium not only enhances proliferation but also counteracts the down-regulation of NKG2D, more so than the addition of IL-2. These results indicate that NKG2D can regulate the priming of human naive CD8+ T cells, which may provide an alternative mechanism for potentiating and channeling the immune response.

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