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Association of CTLA4 Gene Polymorphisms with Susceptibility and Pathology Correlation to Pulmonary Tuberculosis in Southern Han Chinese

机译:CTLA4基因多态性与南方汉族人群肺结核易感性和病理相关性的关系

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The cytotoxic T lymphocyte antigen-4 (CTLA4) gene is a key negative regulator of the T lymphocyte immune response. It has been found that CTLA4 +49A>G (rs231775), +6230G>A (rs3087243), and 11430G>A (rs 11571319) polymorphisms are associated with susceptibility to many autoimmune diseases, and can down-regulate the inhibition of cellular immune response of CTLA4. Three SNPs in CTLA4 were genotyped by using the PCR and DNA sequencing methods in order to reveal the susceptibility and pathology correlation to pulmonary tuberculosis in Southern Han Chinese. We found that the frequency of CTLA4 +49AG genotype in the pulmonary tuberculosis patients (38.42%) was significantly lower than that of the healthy controls (49.77%), (P_(cor)=0.038, OR 0.653, 95% C 0.436-0.978). But, no associations were found between the other 2 SNPs (+6230G>A, 11431G>A) and tuberculosis (P>0.05). Haplotype analysis showed that the frequency of haplotype AGG in the healthy controls group (6.9%) was significantly higher than the pulmonary tuberculosis patients group (1.4%), (global P=0.005, P_(cor)=0.0002, OR 0.183, 95% Cl 0.072-0.468). In addition, haplotype GGA was found to be significantly related to tuberculosis with double lung lesion rather than single lung lesion (P_(cor)=0.042). This study is the first to report that genetic variants in the CTLA4 gene can be associated with pulmonary tuberculosis in Southern Han Chinese, and CTLA4 +49AG genotype as well as haplotype AGG may reduce the risk of being infected with pulmonary tuberculosis. The GGA haplotype was related to tuberculosis with double lung lesion, which provides a new experimental basis to clarify the pathogenesis of pulmonary tuberculosis.
机译:细胞毒性T淋巴细胞抗原4(CTLA4)基因是T淋巴细胞免疫反应的关键负调控因子。已经发现CTLA4 + 49A> G(rs231775),+ 6230G> A(rs3087243)和11430G> A(rs 11571319)多态性与许多自身免疫性疾病的易感性有关,并且可以下调细胞免疫的抑制作用CTLA4的响应。通过PCR和DNA测序方法对CTLA4中的3个SNP进行基因分型,以揭示南方汉族人群与肺结核的易感性和病理相关性。我们发现肺结核患者中CTLA4 + 49AG基因型的频率(38.42%)显着低于健康对照组的频率(49.77%),(P_(cor)= 0.038,或0.653,95%C 0.436- 0.978)。但是,其他2个SNPs(+ 6230G> A,11431G> A)与结核病之间没有关联(P> 0.05)。单倍型分析显示,健康对照组的单倍型AGG频率(6.9%)明显高于肺结核患者组(1.4%),(整体P = 0.005,P_(cor)= 0.0002,OR 0.183,95% Cl 0.072-0.468)。此外,发现单倍型GGA与具有双肺病变而不是单肺病变的结核病显着相关(P_(cor)= 0.042)。这项研究是第一个报道CTLA4基因的遗传变异可能与南方汉族人肺结核有关的研究,而CTLA4 + 49AG基因型和单倍型AGG可以降低感染肺结核的风险。 GGA单倍型与结核合并双肺病变有关,为阐明肺结核的发病机理提供了新的实验依据。

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