The role of Syk/CARD9 coupled C-type lectins in antifungal immunity

被引:191
作者
Drummond, Rebecca A. [1 ]
Saijo, Shinobu [2 ]
Iwakura, Yoichiro [3 ]
Brown, Gordon D. [1 ]
机构
[1] Univ Aberdeen, Aberdeen Fungal Grp, Sect Immun & Infect, Inst Med Sci, Aberdeen AB25 2ZD, Scotland
[2] Chiba Univ, Med Mycol Res Ctr, Div Mol Immunol, Chuo Ku, Chiba, Japan
[3] Univ Tokyo, Inst Med Sci, Ctr Expt Med & Syst Biol, Minato Ku, Tokyo, Japan
基金
英国惠康基金; 英国医学研究理事会;
关键词
Antifungal immunity; Dectin-1; Dectin-2; Mincle; CHRONIC MUCOCUTANEOUS CANDIDIASIS; PATTERN-RECOGNITION RECEPTOR; HOST-DEFENSE; DECTIN-2; RECOGNITION; ACTIVATING RECEPTOR; NLRP3; INFLAMMASOME; EXPRESSION; INNATE; CELLS; INDUCTION;
D O I
10.1002/eji.201041252
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Fungal infections are affecting an increasing number of people, and the failure of current therapies in treating systemic infection has resulted in an unacceptably high mortality rate. It is therefore of importance that we understand immune mechanisms operating during fungal infections, in order to facilitate development of adjunctive immunotherapies for the treatment of these diseases. C-type lectin receptors (CLRs) are pattern recognition receptors (PRRs) that are critical for immune responses to fungi. Many of these receptors are coupled to Syk kinase, which allows these receptors to signal via CARD9 leading to NF-kappa B activation, which in turn contributes to the induction of both innate and adaptive immunity. Dectin-1, Dectin-2 and Mincle are all CLRs that share this common signalling mechanism and have been shown to play key roles in antifungal immunity. This review aims to update existing paradigms and summarise the most recent findings on these CLRs, their signal transduction mechanisms and the collaborations between these CLRs and other PRRs.
引用
收藏
页码:276 / 281
页数:6
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