Hurst Julia, von Landenberg Philipp
Institut für Klinische Chemie und Laboratoriumsmedizin, Johannes Gutenberg Universität Mainz, Langenbeckstrasse 1, 55131 Mainz, Germany.
Autoimmun Rev. 2008 Jan;7(3):204-8. doi: 10.1016/j.autrev.2007.11.006. Epub 2007 Dec 4.
The understanding of autoimmune diseases experienced an impressive boost since the Toll-like receptors (TLRs) have been identified as possible key players in autoimmune pathophysiology. Although these receptors recognize a variety of structures derived from viruses, bacteria and fungi leading to subsequent initiation of the relevant immune responses recent data support the idea that TLRs are crucial in the induction and perpetuation of certain autoimmune diseases, especially the systemic lupus erythematosus (SLE). In this review we will summarize recent data on involvement of TLRs in the development of autoimmune diseases. This review will focus on TLRs 7, 8 and 9 which were originally identified as receptors specific for bacterial and viral RNA/DNA, but more recent in vitro and in vivo studies have linked these receptors to the detection of host RNA, DNA, and RNA- or DNA-associated proteins in the context of autoimmunity.
自从Toll样受体(TLRs)被确定为自身免疫病理生理学中可能的关键参与者以来,对自身免疫性疾病的理解有了显著的提升。尽管这些受体识别来自病毒、细菌和真菌的多种结构,从而引发相关的免疫反应,但最近的数据支持这样一种观点,即TLRs在某些自身免疫性疾病,特别是系统性红斑狼疮(SLE)的诱导和持续发展中至关重要。在这篇综述中,我们将总结关于TLRs参与自身免疫性疾病发展的最新数据。本综述将聚焦于TLR7、TLR8和TLR9,它们最初被确定为细菌和病毒RNA/DNA的特异性受体,但最近的体外和体内研究已将这些受体与自身免疫背景下宿主RNA、DNA以及RNA或DNA相关蛋白的检测联系起来。