Alexopoulou Lena, Desnues Benoit, Demaria Olivier
Centre D'immunologie de Marseille-Luminy, Aix-Marseille Université, case 906, 13288 Marseille Cedex 9, France.
Med Sci (Paris). 2012 Jan;28(1):96-102. doi: 10.1051/medsci/2012281023. Epub 2012 Jan 27.
Toll-like receptors (TLR) sense a variety of microbial products and play an important role in the mounting of innate and adaptive immune responses. TLR1 to TLR9 are common in mice and humans and recognize similar ligands in both species, with the exception of TLR8. Human TLR7 and TLR8 and mouse TLR7 detect viral single-stranded RNA and imidazoquinoline compounds, while mouse TLR8 not. Based on this discrepancy, for long time it was believed that mouse TLR8 is not functional and as a consequence the contribution of TLR8 to innate immunity remained poorly understood. Our recent studies revealed an important role for TLR8 in the regulation of TLR7-mediated autoimmunity in the mouse. This review illustrates our current understanding regarding the function of TLR8 and its potential for future clinical use for the treatment and/or prevention of various pathological conditions.
Toll样受体(TLR)可识别多种微生物产物,并在固有免疫和适应性免疫反应的启动中发挥重要作用。TLR1至TLR9在小鼠和人类中普遍存在,且在这两个物种中识别相似的配体,但TLR8除外。人类TLR7和TLR8以及小鼠TLR7可检测病毒单链RNA和咪唑喹啉化合物,而小鼠TLR8则不能。基于这种差异,长期以来人们认为小鼠TLR8没有功能,因此TLR8对固有免疫的贡献仍知之甚少。我们最近的研究揭示了TLR8在调节小鼠TLR7介导的自身免疫中的重要作用。这篇综述阐述了我们目前对TLR8功能的理解及其在未来临床治疗和/或预防各种病理状况中的潜在应用。