O'Neill Luke A J
School of Biochemistry and Immunology, Trinity College Dublin, Ireland.
Curr Opin Immunol. 2006 Feb;18(1):3-9. doi: 10.1016/j.coi.2005.11.012. Epub 2005 Dec 15.
Signal transduction pathways activated by Toll-like receptors (TLRs) have continued to be a major focus of research for investigators interested in the initiation of innate immune responses and the induction of pro-inflammatory cytokines and type I interferons during infection. Biochemical details of the major signalling pathways have now been obtained, and the specific signalling pathways activated by different TLRs are being elucidated. New insights into the activation of IRF family members, notably IRF3, IRF5 and IRF7, have been obtained, and interesting spatiotemporal aspects of signalling by MyD88 leading to IRF7 activation revealed. Adapters in TLR signalling are targets for inhibition, both by endogenous regulators and by virally derived proteins. Selective targeting of pathways by anti-inflammatory glucocorticoids also indicates the potential for modulating TLR signalling therapeutically.
对于那些对感染期间先天免疫反应的启动以及促炎细胞因子和I型干扰素的诱导感兴趣的研究人员来说,Toll样受体(TLR)激活的信号转导通路一直是主要的研究焦点。目前已经获得了主要信号通路的生化细节,并且不同TLR激活的特定信号通路也正在被阐明。对于IRF家族成员(尤其是IRF3、IRF5和IRF7)的激活有了新的认识,并且揭示了MyD88信号传导导致IRF7激活的有趣时空方面。TLR信号传导中的衔接蛋白是内源性调节因子和病毒衍生蛋白抑制的靶点。抗炎糖皮质激素对通路的选择性靶向也表明了治疗性调节TLR信号传导的潜力。