TNFalpha启动子-238和-308位点的单核苷酸多态性(snp):麻风病的临床和细菌学评价

Patrícia R Vanderborght, Haroldo J Matos, Ana M Salles, Sidra E Vasconcellos, Valcemir F Silva-Filho, Tom W J Huizinga, Tom H M Ottenhoff, Elisabeth P Sampaio, Euzenir N Sarno, Adalberto R Santos, Milton O Moraes
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引用次数: 15

摘要

肿瘤坏死因子α (TNFalpha)在协调炎症和免疫反应的复杂事件中起着关键作用。TNFa基因启动子区域内的单核苷酸多态性(snp)与许多疾病有关。本研究的目的是研究TNFalpha启动子-238 (G/A)和-308 (G/A)位点多态性的分布及其与不同临床形式麻风预后的关系。此外,我们还对基因型多菌(MB)患者的细菌学指数(BI)进行了评估,以探讨每种多态性对细菌负荷的可能影响。本研究共纳入631例麻风患者,其中401例为MB, 230例为少杆菌(PB),根据其种族(非洲裔和欧洲裔巴西人)进一步分离。单倍型中snp的组合产生了三种不同的排列:TNFG-G、TNFG-A和TNFA-G。尽管单倍型的频率在种族上有显著差异,但在MB和PB患者之间的单倍型频率没有统计学差异。BI分析显示-308携带者的细菌学指数较低,而-238携带者的BI较高。虽然在本分析中没有发现多态性对临床结果发展的影响,但似乎在不同的阶段(在MB患者中),多态性可能有助于观察到的严重程度。
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Single nucleotide polymorphisms (SNPs) at -238 and -308 positions in the TNFalpha promoter: clinical and bacteriological evaluation in leprosy.

Tumor necrosis factor alpha (TNFalpha) plays a key role in orchestrating the complex events involved in inflammation and immune response. The presence of single nucleotide polymorphisms (SNPs) within the promoter region of the TNFa gene has been associated with a number of diseases. The aim of this study was to investigate the distribution of polymorphisms at positions -238 (G/A) and -308 (G/A) at the TNFalpha promoter, and its association to the outcome of different clinical forms of leprosy. Furthermore, the bacteriological index (BI) was evaluated among genotyped multibacillary (MB) patients in order to investigate the possible influence of each polymorphism on the bacterial load. This study included a total of 631 leprosy patients being 401 MB and 230 paucibacillary (PB), that was further separated according to its ethnicity (Afro- and Euro-Brazilians). The combination of SNPs in haplotypes generated three different arrangements: TNFG-G, TNFG-A and TNFA-G. In spite of the marked differences observed in the frequency of the haplotypes along the ethnic groups, no statistical differences were observed in haplotype frequencies between MB and PB patients. The BI analyses showed a lower bacteriological index among the -308 carriers, while the BI of the -238 carriers was higher. Although no significance has been achieved in this analysis regarding the influence of the polymorphisms to the development of the clinical outcome, it seems that in a different stage (among the MB patients) the polymorphisms could contribute to the degree of severity observed.

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