Targeting Toll-like receptors with small molecule agents

被引:96
作者
Wang, Xiaohui
Smith, Christina
Yin, Hang [1 ]
机构
[1] 596 Univ Colorado Boulder, Dept Chem & Biochem, Boulder, CO 80309 USA
基金
美国国家卫生研究院;
关键词
SIGNALING INHIBITORS; INFLAMMATORY RESPONSE; MONOACYL LIPOPEPTIDES; CYTOKINE PRODUCTION; DECOY PEPTIDES; LIPID-A; TLR4; TAK-242; BINDING; MD-2;
D O I
10.1039/c3cs60039d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Toll-like receptors (TLRs) are type I transmembrane proteins that are key regulators of both innate and adaptive immune responses. To protect the host from viral and bacterial threats, TLRs trigger a pro-inflammatory immune response by detecting pathogen and danger associated molecular patterns. Considerable evidence has accumulated to show that the dysregulation of TLR signaling contributes to the development and progression of numerous diseases. Therefore, TLRs are emerging as important drug discovery targets. Currently, there is great interest in the development of TLR small molecule modulators for interrogating TLR signaling and treating diseases caused by TLR signaling malfunctions. In this tutorial review, we will outline methods for the discovery of TLR small molecule modulators and the up-to-date progress in this field. Small molecules targeting TLRs not only provide an opportunity to identify promising drug candidates, but also unveil knowledge regarding TLR signaling pathways.
引用
收藏
页码:4859 / 4866
页数:8
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