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Biomed Rep. 2017 Jun;6(6):698-702. doi: 10.3892/br.2017.908. Epub 2017 May 9.
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Associations of potentially functional variants in IL-6, JAKs and STAT3 with gastric cancer risk in an eastern Chinese population.白细胞介素-6、JAK激酶和信号转导与转录激活因子3中潜在功能性变体与中国东部人群胃癌风险的关联。
Oncotarget. 2016 May 10;7(19):28112-23. doi: 10.18632/oncotarget.8492.
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High IL-6 and low IL-15 levels mark the presence of TB infection: A preliminary study.高白细胞介素-6和低白细胞介素-15水平标志着结核感染的存在:一项初步研究。
Cytokine. 2016 May;81:57-62. doi: 10.1016/j.cyto.2016.02.003. Epub 2016 Feb 13.
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Single Nucleotide Polymorphisms in IL17A and IL6 Are Associated with Decreased Risk for Pulmonary Tuberculosis in Southern Brazilian Population.白细胞介素17A和白细胞介素6中的单核苷酸多态性与巴西南部人群患肺结核风险降低相关。
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Genetic background affects the expansion of macrophage subsets in the lungs of Mycobacterium tuberculosis-infected hosts.遗传背景影响结核分枝杆菌感染宿主肺部巨噬细胞亚群的扩增。
Immunology. 2016 May;148(1):102-13. doi: 10.1111/imm.12591.
6
IRGM gene polymorphisms and haplotypes associate with susceptibility of pulmonary tuberculosis in Chinese Hubei Han population.IRGM基因多态性和单倍型与中国湖北汉族人群肺结核易感性相关。
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MicroRNA-365 in macrophages regulates Mycobacterium tuberculosis-induced active pulmonary tuberculosis via interleukin-6.巨噬细胞中的微小RNA-365通过白细胞介素-6调节结核分枝杆菌诱导的活动性肺结核。
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The -137G/C single nucleotide polymorphism in IL-18 gene promoter contributes to tuberculosis susceptibility in Chinese Han population.白细胞介素-18基因启动子区域的-137G/C单核苷酸多态性与中国汉族人群的结核病易感性相关。
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10
Genetic Polymorphisms in Inflammasome-Dependent Innate Immunity among Pediatric Patients with Severe Renal Parenchymal Infections.重症肾实质感染儿科患者炎性小体依赖性固有免疫中的基因多态性
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中国汉族人群中 和 的遗传多态性与肺结核的关系。

Genetic Polymorphisms of and in a Chinese Han Population with Pulmonary Tuberculosis.

机构信息

Department of Respiratory and Critical Care Medicine, West China Hospital, Sichuan University, Chengdu, Sichuan, China.

Department of Radiology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.

出版信息

Biomed Res Int. 2018 May 14;2018:3010898. doi: 10.1155/2018/3010898. eCollection 2018.

DOI:10.1155/2018/3010898
PMID:29888256
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5977055/
Abstract

BACKGROUND

The factors that predispose to pulmonary tuberculosis (PTB) are not fully understood. Previous studies have shown that cytokine gene polymorphisms were associated with PTB.

OBJECTIVES

In this study, we have investigated the relationship between , and polymorphisms and a predisposition to (MTB) infection and PTB.

METHODS

A total of 209 cases of PTB, 201 subjects with latent TB infection (LTBI), and 204 healthy controls (HCS) were included in this study. Logistic regression analyses under allelic, homozygous, and heterozygous models were used to calculate values, odds ratios (ORs), and 95% confidence intervals (CIs) for assessing the association between single nucleotide polymorphisms (SNPs) and disease risk, adjusting for sex and age. Genotyping was conducted using the improved multiplex ligase detection reaction (iMLDR) method.

RESULTS

When comparing PTB patients with LTBI subjects, significant associations with disease development were observed for SNPs of and . When comparing LTBI subjects with HCS, polymorphisms were significantly associated with LIBI. Haplotype analyses suggested that the CGG haplotype of was associated with an increased risk of PTB ( = 0.039, OR = 1.34, 95% CI: 1.01-1.76), while the TTGCG haplotype of was a protective factor against PTB ( = 0.039, OR = 0.66, 95% CI: 0.44-0.98).

CONCLUSION

Our study demonstrated that variants were related to LTBI and and variants were associated with PTB.

摘要

背景

导致肺结核(PTB)的因素尚未完全阐明。既往研究表明细胞因子基因多态性与 PTB 相关。

目的

本研究旨在探讨 、 及 基因多态性与结核分枝杆菌(MTB)感染及 PTB 易感性的关系。

方法

共纳入 209 例 PTB 患者、201 例潜伏性结核感染(LTBI)患者和 204 例健康对照者。采用等位基因、纯合子和杂合子模型的 logistic 回归分析,计算各单核苷酸多态性(SNP)与疾病风险的 值、比值比(OR)及其 95%置信区间(CI),以调整性别和年龄因素。采用改良多重连接酶检测反应(iMLDR)方法进行基因分型。

结果

与 LTBI 患者相比,PTB 患者的 及 基因 SNP 与疾病发展显著相关。与 HCS 相比,LTBI 患者的 基因 SNP 与 LTBI 显著相关。单体型分析提示 基因的 CGG 单体型与 PTB 风险增加相关( = 0.039,OR = 1.34,95%CI:1.01-1.76),而 基因的 TTGCG 单体型是 PTB 的保护因素( = 0.039,OR = 0.66,95%CI:0.44-0.98)。

结论

本研究表明 基因变体与 LTBI 相关, 及 基因变体与 PTB 相关。