Akashi-Takamura Sachiko, Miyake Kensuke
Division of Infectious Genetics, The Institute of Medical Science, The University of Tokyo, 4-6-1, Shirokanedai, Minatoku, Tokyo, 108-8639, Japan.
J Infect Chemother. 2006 Oct;12(5):233-40. doi: 10.1007/s10156-006-0477-4. Epub 2006 Nov 6.
Upon the invasion of pathogens, the immune system needs to mount defense responses immediately. Over the past 10 years, Toll-like receptors (TLRs) have been discovered in mammals and defined as pathogen sensors. TLRs are considered to bind directly to ligands, discriminate them immediately, and induce defense responses when appropriate. We here review microbial recognition by TLRs, downstream signaling, and the relationship of TLRs to susceptibility to infectious diseases and immune disorders. Recent reports have revealed a requirement for co-receptors in TLR responses. A TLR signaling pathway is required for protection against infectious diseases, but excessive signaling may lead to allergies, autoimmune diseases, or atherosclerosis. In humans, several deficiencies of signaling molecules downstream of TLRs, and TLR polymorphisms that affect recognition or signaling, were reported to cause immunodeficiencies. It is important to understand how TLR signaling is controlled.
病原体入侵时,免疫系统需要立即启动防御反应。在过去10年里,Toll样受体(TLRs)在哺乳动物中被发现,并被定义为病原体传感器。TLRs被认为可直接与配体结合,立即识别它们,并在适当的时候诱导防御反应。我们在此综述TLRs介导的微生物识别、下游信号传导以及TLRs与传染病易感性和免疫紊乱的关系。最近的报道揭示了TLRs反应中对共受体的需求。TLR信号通路对于抵御传染病是必需的,但过度的信号传导可能导致过敏、自身免疫性疾病或动脉粥样硬化。在人类中,据报道TLRs下游信号分子的几种缺陷以及影响识别或信号传导的TLR多态性会导致免疫缺陷。了解TLR信号传导如何被控制很重要。