首页> 外文期刊>Autoimmunity >Two SNPs in NLRP3 gene are involved in the predisposition to type-1 diabetes and celiac disease in a pediatric population from northeast Brazil.
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Two SNPs in NLRP3 gene are involved in the predisposition to type-1 diabetes and celiac disease in a pediatric population from northeast Brazil.

机译:在巴西东北部的一个儿科人群中,NLRP3基因中的两个SNP参与了1型糖尿病和腹腔疾病的易感性。

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Recent findings provide evidence of the critical role of innate immunity NALP1/NLRP1 and NALP3/NLRP3/CIAS1 genes in inflammatory diseases, and also in the predisposition to autoimmune disorders. We evaluated the possible association of five single nucleotide polymorphisms (SNPs), two in NLRP1 gene and three in NLRP3 gene, in pediatric patients from the north eastern region of Brazil affected by type-1 diabetes (T1D, n = 196), celiac disease (CD, n = 59), and atopic dermatitis (AD, n = 165), and in healthy individuals (n = 192). Our results demonstrated that NLRP3 rs10754558 SNP was associated specifically to T1D (p = 4exp-3) and NLRP3 rs358294199 SNP to CD (p = 5exp-4) in the Brazilian population. Despite its strong association with T1D in Norwegian population, NLRP1 was not associated with T1D, in the Brazilian population. According to previous studies in Caucasoid cohorts, NLRP1 and NLRP3 seemed not to be associated to AD. Since it has been reported that IL-1 beta has a systemic effect in the lost of the immunologic tolerance and that NALP3 inflammasome is directly involved in the production of this pro-inflammatory cytokine, we hypothesized that variations in NLRP3 could belong to a predisposing genetic background that contribute to the development of autoimmune diseases.
机译:最近的发现提供了先天免疫力NALP1 / NLRP1和NALP3 / NLRP3 / CIAS1基因在炎性疾病以及自身免疫疾病易感性中的关键作用的证据。我们评估了巴西东北部受1型糖尿病(T1D,n = 196)影响的腹腔疾病的儿科患者中五个单核苷酸多态性(SNP),NLRP1基因中的两个和NLRP3基因中的三个可能的关联(CD,n = 59),特应性皮炎(AD,n = 165)和健康个体(n = 192)。我们的结果表明,巴西人群中NLRP3 rs10754558 SNP与T1D(p = 4exp-3)和NLRP3 rs358294199 SNP与CD(p = 5exp-4)特别相关。尽管在挪威人口中与T1D密切相关,但在巴西人口中,NLRP1与T1D不相关。根据以前在高加索人群中的研究,NLRP1和NLRP3似乎与AD无关。由于有报道说IL-1β对失去免疫耐受具有系统性作用,而NALP3炎性小体直接参与了这种促炎性细胞因子的产生,我们推测NLRP3的变异可能属于易感基因自身免疫疾病发展的背景。

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