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本文引用的文献

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Innate immune recognition of Mycobacterium tuberculosis.结核分枝杆菌的天然免疫识别
Clin Dev Immunol. 2011;2011:405310. doi: 10.1155/2011/405310. Epub 2011 Apr 7.
2
Incidence of infectious diseases and survival among the Roma population: a longitudinal cohort study.罗姆人人口中的传染病发病率和生存情况:一项纵向队列研究。
Eur J Public Health. 2012 Apr;22(2):262-6. doi: 10.1093/eurpub/ckq204. Epub 2011 Jan 7.
3
Toll-like receptors, tumor necrosis factor-α, and interleukin-10 gene polymorphisms in risk of pulmonary tuberculosis and disease severity.Toll 样受体、肿瘤坏死因子-α 和白细胞介素-10 基因多态性与肺结核发病风险及疾病严重程度的关系。
Hum Immunol. 2010 Oct;71(10):1005-10. doi: 10.1016/j.humimm.2010.07.009. Epub 2010 Jul 30.
4
Toll-like receptor 2 (P631H) mutant impairs membrane internalization and is a dominant negative allele.Toll 样受体 2(P631H)突变体损害膜内化,是一个显性负等位基因。
Scand J Immunol. 2010 May;71(5):369-81. doi: 10.1111/j.1365-3083.2010.02379.x.
5
Lack of association of Toll-Like Receptor 2 Arg753Gln with cutaneous leishmaniasis.Toll样受体2基因Arg753Gln与皮肤利什曼病无关联
Parasitol Int. 2010 Sep;59(3):466-8. doi: 10.1016/j.parint.2010.03.008. Epub 2010 Apr 11.
6
Possible underlying mechanisms for successful emergence of the Mycobacterium tuberculosis Beijing genotype strains.结核分枝杆菌北京基因型菌株成功出现的可能潜在机制。
Lancet Infect Dis. 2010 Feb;10(2):103-11. doi: 10.1016/S1473-3099(09)70330-5.
7
Toll-like receptors 2 and 4 gene polymorphisms in a southeastern Chinese population with tuberculosis.中国东南部地区结核病患者 Toll 样受体 2 和 4 基因多态性研究。
Int J Immunogenet. 2010 Apr;37(2):135-8. doi: 10.1111/j.1744-313X.2009.00892.x. Epub 2009 Dec 3.
8
The heterogeneous allelic repertoire of human toll-like receptor (TLR) genes.人类 toll 样受体 (TLR) 基因的异质等位基因库。
PLoS One. 2009 Nov 17;4(11):e7803. doi: 10.1371/journal.pone.0007803.
9
No association of the TLR2 gene Arg753Gln polymorphism with rheumatic heart disease and Behçet's disease.TLR2 基因 Arg753Gln 多态性与风湿性心脏病和贝赫切特病无关。
Clin Rheumatol. 2009 Dec;28(12):1385-8. doi: 10.1007/s10067-009-1252-6. Epub 2009 Aug 21.
10
Toll-like receptors and innate immunity.Toll样受体与天然免疫
Biochem Biophys Res Commun. 2009 Oct 30;388(4):621-5. doi: 10.1016/j.bbrc.2009.08.062. Epub 2009 Aug 15.

不同族群和地理起源人群 Toll 样受体 2 多态性的不同模式。

Different patterns of Toll-like receptor 2 polymorphisms in populations of various ethnic and geographic origins.

机构信息

Department of Internal Medicine, Radboud University Nijmegen Medical Centre, Radboud University, Nijmegen, Netherlands.

出版信息

Infect Immun. 2012 May;80(5):1917-22. doi: 10.1128/IAI.00121-12. Epub 2012 Feb 21.

DOI:10.1128/IAI.00121-12
PMID:22354034
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3347449/
Abstract

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.

摘要

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。