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首页> 外文期刊>Journal of gastroenterology and hepatology >LMP2/LMP7 gene variant: A risk factor for intestinal Mycobacterium tuberculosis infection in the Chinese population.
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LMP2/LMP7 gene variant: A risk factor for intestinal Mycobacterium tuberculosis infection in the Chinese population.

机译:LMP2 / LMP7基因变异:在中国人群中肠结核分枝杆菌感染的危险因素。

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Background and Aims: Low molecular mass protein-2 (LMP2) and low molecular mass protein-7 (LMP7) genes play a critical role in foreign antigen processing on the major histocompatibility complex-I CD8(+) cytotoxic T-lymphocyte pathway. This study was designed to investigate whether the sequence variants in the LMP2/LMP7 coding region were associated with intestinal Mycobacterium tuberculosis (M. tuberculosis) infection or with the co-infection of pulmonary tuberculosis. Methods: A total of 168 patients with intestinal tuberculosis and 235 normal controls were recruited for this study. Two polymorphisms of LMP2 (Arg60-His) and LMP7 (Gln145-Lys) were identified by polymerase chain reaction-restriction fragment length polymorphism method. The associations of the LMP2/LMP7 genotype and haplotype with intestinal M. tuberculosis infection were assessed by using logistic regression analysis. Results: The results revealed that LMP7 position codon 145 Lys/Lys and Gln/Lys alleles in the coding region were associated with the infection of intestinal M. tuberculosis (P = 0.003, odds ratio [OR] = 3.86 and P < 0.001, OR = 2.28, respectively). Meanwhile, the Arg-Lys and Cys-Lys haplotypes exhibited significant relation to the intestinal M. tuberculosis infection (P = 0.006, OR = 1.87; P = 0.021, OR = 1.83, respectively). No significant associations were observed for any of the single-nucleotide polymorphism genotypes or haplotypes with the co-infection of pulmonary tuberculosis (P > 0.05). Conclusions: The results indicated that the genetic variant within the LMP2/LMP7 gene would increase the risk of intestinal M. tuberculosis infection.
机译:背景与目的:低分子蛋白2(LMP2)和低分子蛋白7(LMP7)基因在主要组织相容性复合物-CD8(+)细胞毒性T淋巴细胞途径的外源抗原加工中起关键作用。这项研究旨在调查LMP2 / LMP7编码区中的序列变异是否与肠道结核分枝杆菌(M. tuberculosis)感染或肺结核的共感染有关。方法:本研究共招募了168名肠结核患者和235名正常对照。通过聚合酶链反应-限制性片段长度多态性方法鉴定了LMP2(Arg60-His)和LMP7(Gln145-Lys)的两个多态性。 LMP2 / LMP7基因型和单倍型与肠道结核分枝杆菌感染的相关性通过逻辑回归分析进行评估。结果:结果显示,编码区中的LMP7位置密码子145 Lys / Lys和Gln / Lys等位基因与肠道结核分枝杆菌的感染有关(P = 0.003,优势比[OR] = 3.86和P <0.001,OR分别为2.28)。同时,Arg-Lys和Cys-Lys单倍型与肠道结核分枝杆菌感染表现出显着相关性(分别为P = 0.006,OR = 1.87; P = 0.021,OR = 1.83)。没有发现任何单核苷酸多态性基因型或单倍型与肺结核的合并感染有显着相关性(P> 0.05)。结论:结果表明,LMP2 / LMP7基因内的遗传变异将增加肠道结核分枝杆菌感染的风险。

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