Brighton and Sussex Medical School, Trafford Centre, Sussex University, Falmer, Brighton BN1 9RY, UK.
Curr Drug Targets. 2009 Nov;10(11):1139-55. doi: 10.2174/138945009789735101.
In the past few years there has been an increasing appreciation of the importance of Toll-like receptors (TLRs), not just in immunity, but also in autoimmune diseases. TLRs were first identified as sensors of viral and bacterial pathogens that form an integral part of the innate immune response. It was later discovered that these receptors can also respond to endogenous ligands that are produced as a result of tissue damage. This lead to the hypothesis that TLRs may be key contributors to the pathogenesis of chronic inflammatory conditions. A large body of data supporting the role of TLRs in autoimmunity has emerged from animal models and more data is increasingly being generated from human studies as further tools to examine these receptors have become available. Developing strategies to manipulate TLR function is of great interest in autoimmunity, as well as other diseases that include allergy and cancer. This review explores the evidence that points to a role for TLRs in autoimmunity and highlights some of the potential ways in which modulation of their action may yield clinical benefits.
在过去的几年中,人们越来越认识到 Toll 样受体 (TLRs) 的重要性,不仅在免疫方面,而且在自身免疫性疾病方面也是如此。TLRs 最初被鉴定为病毒和细菌病原体的传感器,是先天免疫反应的重要组成部分。后来发现,这些受体也可以对由于组织损伤而产生的内源性配体作出反应。这就提出了一个假设,即 TLR 可能是慢性炎症性疾病发病机制的关键因素。大量支持 TLR 在自身免疫中的作用的数据已经从动物模型中出现,并且随着更多的工具可用于研究这些受体,来自人类研究的数据也在不断增加。在自身免疫以及包括过敏和癌症在内的其他疾病中,操纵 TLR 功能的策略具有很大的研究意义。本综述探讨了 TLR 在自身免疫中的作用的证据,并强调了调节其作用的一些潜在方法可能带来临床益处。