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The role of TLR9 polymorphism in susceptibility to pulmonary tuberculosis

机译:TLR9基因多态性在肺结核易感性中的作用

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摘要

Mycobacterium tuberculosis (MTB) is the causative agent of pulmonary tuberculosis (PTB), a major health problem that leads to 1.5 million deaths annually. Host genetic factors play a significant role in disease resistance/ susceptibility by altering immunity against MTB. Toll-like receptor (TLR) sensors such as TLR2, TLR4, TLR8, and TLR9 are known to play a pivotal role in PTB via modulating sensor expression and/or effector responses. Single-nucleotide polymorphism (SNP) rs187084 (T-1486C) of the TLR9 promoter is associated with various autoimmune disorders and cancers. A recent bioinformatic analysis predicted that the T-1486C SNP is involved in PTB, although its potential role is unclear. To investigate the role of T-1486C in PTB, we stimulated PBMCs with the H37Rv whole cell lysate. We found that the presence of the "C" allele increases the tran-scriptional activity of the TLR9, which in turn induces high levels of Interferon gamma-induced protein 10 (IP-10), a biomarker for PTB.
机译:结核分枝杆菌(MTB)是肺结核(PTB)的病原体,这是一个主要的健康问题,每年导致150万人死亡。宿主遗传因子通过改变对MTB的免疫力,在抗病性/易感性中起重要作用。诸如TLR2,TLR4,TLR8和TLR9之类的收费型受体(TLR)传感器通过调节传感器表达和/或效应子响应在PTB中起关键作用。 TLR9启动子的单核苷酸多态性(SNP)rs187084(T-1486C)与各种自身免疫性疾病和癌症有关。最近的生物信息学分析预测T-1486C SNP参与了PTB,尽管其潜在作用尚不清楚。为了研究T-1486C在PTB中的作用,我们用H37Rv全细胞裂解物刺激了PBMC。我们发现“ C”等位基因的存在增加了TLR9的转录活性,进而诱导了高水平的干扰素γ诱导蛋白10(IP-10),PTB的生物标志物。

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