Zhang Jianping, Yang Jingping, Xu Xiyuan, Liang Liangshen, Sun Haixia, Liu Guohua, Zhang Lihong, Su Yun
Department of Critical Medicine, Ordos Central Hospital, Ordos, Inner Mongolia Autonomous Region 014010, P.R. China.
Department of Respiratory and Critical Medicine, The Third Affiliated Hospital of Inner Mongolia Medical University, Baotou, Inner Mongolia Autonomous Region 014010, P.R. China.
Exp Ther Med. 2016 Jan;11(1):131-139. doi: 10.3892/etm.2015.2884. Epub 2015 Nov 19.
The present study aimed to investigate whether genetic polymorphisms in the Toll-like receptor (TLR)-4 and Toll/interleukin-1 receptor (TIR)-associated protein (TIRAP) genes, and/or their expression levels, influence the susceptibility of a patient to sepsis. A total of 106 patients with sepsis were divided into two groups on the basis of their acute physiology and chronic health evaluation (APACHE) II scores: i) Sepsis group A (APACHE II <20) and ii) Sepsis group B (APACHE II >20). In addition, 100 healthy volunteers were enrolled into the control group. Polymerase chain reaction-restriction fragment length polymorphism assay was used to detect the following genetic polymorphisms: The Ser180Leu allele of the TIRAP gene and the Asp299Gly and Thr399I1e alleles of the TLR4 gene. Furthermore, the protein expression levels of TLR4 and TIRAP were analyzed using an enzyme-linked immunosorbent assay. Genetic polymorphisms were not detected for the TLR4 and TIRAP genes; however, the protein expression levels of TLR4 and TIRAP differed significantly between the control, sepsis A and sepsis B groups (P<0.01). An APACHE II score of 20 was used as a baseline in order to differentiate sepsis severity. Pearson analysis demonstrated that TLR4 and TIRAP protein expression levels were positively correlated with sepsis severity (=0.931 and 0.972; P<0.05), and TLR4 protein expression levels were positively correlated with those of TIRAP (=0.936; P<0.05). The results of the present study suggested that the protein expression levels of, but not genetic polymorphisms in, TLR4 and TIRAP were associated with the severity of sepsis.
本研究旨在调查Toll样受体(TLR)-4和Toll/白细胞介素-1受体(TIR)相关蛋白(TIRAP)基因的遗传多态性和/或其表达水平是否会影响患者对败血症的易感性。总共106例败血症患者根据其急性生理与慢性健康状况评估(APACHE)II评分分为两组:i)败血症A组(APACHE II<20)和ii)败血症B组(APACHE II>20)。此外,100名健康志愿者被纳入对照组。采用聚合酶链反应-限制性片段长度多态性分析检测以下遗传多态性:TIRAP基因的Ser180Leu等位基因以及TLR4基因的Asp299Gly和Thr399Ile等位基因。此外,采用酶联免疫吸附测定法分析TLR4和TIRAP的蛋白表达水平。未检测到TLR4和TIRAP基因的遗传多态性;然而,对照组、败血症A组和败血症B组之间TLR4和TIRAP的蛋白表达水平存在显著差异(P<0.01)。以APACHE II评分为20作为基线来区分败血症的严重程度。Pearson分析表明,TLR4和TIRAP蛋白表达水平与败血症严重程度呈正相关(=0.931和0.972;P<0.05),并且TLR4蛋白表达水平与TIRAP的蛋白表达水平呈正相关(=0.936;P<0.05)。本研究结果表明,TLR4和TIRAP的蛋白表达水平而非遗传多态性与败血症的严重程度相关。