A contribution of mouse dendritic cell-derived IL-2 for NK cell activation

被引:169
作者
Granucci, F
Zanoni, I
Pavelka, N
van Dommelen, SLH
Andoniou, CE
Belardelli, F
Esposti, MAD
Ricciardi-Castagnoli, PR
机构
[1] Univ Milano Biocca, Dept Biotechnol & Biosci, I-20126 Milan, Italy
[2] Univ Western Australia, Ctr Ophthalmol & Visual Sci, Immunol & Virol Program, Perth, WA 6009, Australia
[3] Lions Eye Inst, Ctr Expt Immunol, Perth, WA 6009, Australia
[4] Ist Super Sanita, Virol Lab, I-00100 Rome, Italy
基金
英国惠康基金;
关键词
NK cells; dendritic cells; innate immune response; interleukin; 2; interferon gamma;
D O I
10.1084/jem.20040370
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Dendritic cells (DCs) play a predominant role in activation of natural killer (NK) cells that exert their functions against pathogen-infected and tumor cells. Here, we used a murine model to investigate the molecular mechanisms responsible for this process. Two soluble molecules produced by bacterially activated myeloid DCs are required for optimal priming of NK cells. Type I interferons (IFNs) promote the cytotoxic functions of NK cells. IL-2 is necessary both in vitro and in vivo for the efficient production of IFNgamma, which has an important antimetastatic and antibacterial function. These findings provide new information about the mechanisms that mediate DC-NK cell interactions and define a novel and fundamental role for IL-2 in innate immunity.
引用
收藏
页码:287 / 295
页数:9
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