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Cutting edge:: NKG2D is a costimulatory receptor for human naive CD8+ T cells
被引:151
作者:
Maasho, K
[1
]
Opoku-Anane, J
[1
]
Marusina, AI
[1
]
Coligan, JE
[1
]
Borrego, F
[1
]
机构:
[1] NIAID, Receptor Cell Biol Sect, Lab Allerg Dis, NIH, Rockville, MD 20852 USA
关键词:
D O I:
10.4049/jimmunol.174.8.4480
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
In humans, all alpha beta CD8(+) T cells express NKG2D, but in mouse, it is only expressed by activated and memory CD8(+) Tcells. We purified human naive CD8+ Tcells 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+ Tcells, which may provide an alternative mechanism for potentiating and channeling the immune response.
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页码:4480 / 4484
页数:5
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