TLR10: Insights, controversies and potential utility as a therapeutic target

促炎细胞因子 生物 先天免疫系统 TLR2型 Toll样受体 免疫学 炎症 模式识别受体 免疫系统 受体 细胞生物学 遗传学
作者
Si‐Biao Su,Tao Lin,Ze‐Ping Deng,Wen Chen,Shanyu Qin,Hai‐Xing Jiang
出处
期刊:Scandinavian Journal of Immunology [Wiley]
卷期号:93 (4) 被引量:40
标识
DOI:10.1111/sji.12988
摘要

The Toll-like receptor (TLR) family acts as a bridge connecting innate and acquired immunity. TLR10 remains one of the least understood members of this family. Some studies have examined TLR10 ligands, dimerization of TLR10 with other TLRs, and downstream signalling pathways and functions, but they have often arrived at conflicting conclusions. TLR10 can induce the production of proinflammatory cytokines by forming homodimers with itself or heterodimers with TLR1 or other TLRs, but it can also inhibit proinflammatory responses when co-expressed with TLR2 or potentially other TLRs. Mutations in the Toll/Interleukin 1 receptor (TIR) domain of TLR10 alter its signalling activity. Polymorphisms in the TLR10 gene can change the balance between pro- and anti-inflammatory responses and hence modulate the susceptibility to infection and autoimmune diseases. Understanding the full range of TLR10 ligands and functions may allow the receptor to be exploited as a therapeutic target in inflammation- or immune-related diseases. Here, we summarize recent findings on the pro- and anti-inflammatory roles of TLR10 and the molecular pathways in which it is implicated. Our goal is to pave the way for future studies of the only orphan TLR thought to have strong potential as a target in the treatment of inflammation-related diseases.

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