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

机译:CTLA4基因多态性与易受血管结核病的敏感性和病理学相关性

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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淋巴细胞免疫应答的关键负调节剂。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疾病的易感性相关,并且可以降低细胞免疫的抑制CTLA4的响应。 CTLA4中的三个SNP通过使用PCR和DNA测序方法进行基因分型,以揭示与汉族南部肺结核的敏感性和病理相关性。我们发现肺结核患者CTLA4 + 49AG基因型的频率显着低于健康对照(49.77%)(P_(COR)= 0.038,或0.653,95%C 0.436- 0.978)。但是,在其他2个SNP(+ 6230g> A,11431g> A)和结核病之间没有发现任何关联(P> 0.05)。单倍型分析表明,健康对照组(6.9%)中单倍型Agg的频率明显高于肺结核患者组(1.4%)(全球P = 0.005,P_(糖)= 0.0002,或0.183,95% CL 0.072-0.468)。此外,发现单倍型GGA与用双肺病变而不是单肺病变的结核病(P_(COR)= 0.042)显着相关。本研究是第一个报告CTLA4基因中的遗传变异可以与汉族南部肺结核相关的遗传变异,CTLA4 + 49AG基因型以及单倍型AGG可能降低肺结核感染的风险。 GGA单倍型与具有双肺病变的结核病有关,为澄清肺结核发病机制提供了新的实验基础。

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