A role for NKG2D in NK cell-mediated resistance to poxvirus disease

被引:122
|
作者
Fang, Min [1 ]
Lanier, Lewis L. [2 ,3 ]
Sigal, Luis J. [1 ]
机构
[1] Fox Chase Canc Ctr, Program Viral Pathogenesis, Div Basic Sci, Philadelphia, PA 19111 USA
[2] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Canc Res Inst, San Francisco, CA 94143 USA
关键词
NATURAL-KILLER-CELLS; MURINE CYTOMEGALOVIRUS-INFECTION; CD8(+) T-CELLS; ECTROMELIA-VIRUS; ACTIVATION RECEPTOR; CAUSATIVE AGENT; LETHAL MOUSEPOX; FCR-GAMMA; NOD MICE; PATHOGENESIS;
D O I
10.1371/journal.ppat.0040030
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Ectromelia virus ( ECTV) is an orthopoxvirus ( OPV) that causes mousepox, the murine equivalent of human smallpox. C57BL/6 (B6) mice are naturally resistant to mousepox due to the concerted action of innate and adaptive immune responses. Previous studies have shown that natural killer (NK) cells are a component of innate immunity that is essential for the B6 mice resistance to mousepox. However, the mechanism of NK cell-mediated resistance to OPV disease remains undefined. Here we show that B6 mice resistance to mousepox requires the direct cytolytic function of NK cells, as well as their ability to boost the T cell response. Furthermore, we show that the activating receptor NKG2D is required for optimal NK cell-mediated resistance to disease and lethality. Together, our results have important implication towards the understanding of natural resistance to pathogenic viral infections.
引用
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页数:11
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