Department of Internal Medicine, Radboud University Nijmegen Medical Centre, Radboud University, Nijmegen, Netherlands.
Infect Immun. 2012 May;80(5):1917-22. doi: 10.1128/IAI.00121-12. Epub 2012 Feb 21.
Upon the invasion of the host by microorganisms, innate immunity is triggered through pathogen recognition by pattern recognition receptors (PRRs). Toll-like receptors (TLRs) are the best-studied class of PRRs, and they recognize specific pathogen-associated molecular patterns (PAMPs) from various microorganisms. A large number of studies have shown that genetic variation in TLRs may influence susceptibility to infections. We assessed the genetic variation of TLR2, which encodes one of the most important TLRs, in various populations around the globe and correlated it with changes in the function of the molecule. The three best-known nonsynonymous TLR2 polymorphisms (1892C>A, 2029C>T, and 2258G>A) were assessed in different populations from the main continental masses: Romanians, Vlax-Roma, Dutch (European populations), Han Chinese (East Asia), Dogon, Fulani (Africa), and Trio Indians (America). The 2029C>T polymorphism was absent in both European and non-European populations, with the exception of the Vlax-Roma, suggesting that this polymorphism most likely arose in Indo-Aryan people after migration into South Asia. The 1892C>A polymorphism that was found exclusively in European populations, but not in Asian, African, or American volunteers, probably occurred in proto-Indo-Europeans. Interestingly, 2258G>A was present only in Europeans, including Vlax-Roma, but at a very low frequency. The differential pattern of the TLR2 polymorphisms in various populations may explain some of the differences in susceptibility to infections between these populations.
当病原体入侵宿主时,天然免疫会通过模式识别受体(PRRs)识别病原体而被触发。Toll 样受体(TLRs)是研究最充分的 PRR 类别,它们可以识别来自各种微生物的特定病原体相关分子模式(PAMPs)。大量研究表明,TLRs 的遗传变异可能会影响感染的易感性。我们评估了全球不同人群中编码最重要的 TLR 之一的 TLR2 的遗传变异,并将其与分子功能的变化相关联。评估了 TLR2 的三个最著名的非同义 TLR2 多态性(1892C>A、2029C>T 和 2258G>A),这些多态性存在于来自各大洲的不同人群中:罗马尼亚人、Vlax-Roma、荷兰人(欧洲人群)、汉族人(东亚)、多贡人、富拉尼人(非洲)和 Trio 印第安人(美洲)。2029C>T 多态性在欧洲和非欧洲人群中均不存在,除了 Vlax-Roma,这表明这种多态性很可能在印度雅利安人迁移到南亚后出现。仅在欧洲人群中发现的 1892C>A 多态性,但在亚洲、非洲或美洲志愿者中不存在,可能发生在原始印欧人身上。有趣的是,2258G>A 仅存在于欧洲人,包括 Vlax-Roma,但频率非常低。TLR2 多态性在不同人群中的不同模式可能解释了这些人群对感染易感性的一些差异。