Medical Genetic Service, Institute for Maternal and Child Health - IRCCS Burlo Garofolo, Trieste, Italy.
Autoimmunity. 2010 Dec;43(8):583-9. doi: 10.3109/08916930903540432. Epub 2010 Apr 7.
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.
最近的研究结果提供了证据,证明先天免疫 NALP1/NLRP1 和 NALP3/NLRP3/CIAS1 基因在炎症性疾病中,以及在自身免疫性疾病的易感性中起着关键作用。我们评估了巴西东北部地区的 196 例 1 型糖尿病(T1D)、59 例乳糜泻(CD)和 165 例特应性皮炎(AD)患儿以及 192 例健康个体的五个单核苷酸多态性(SNP),其中两个在 NLRP1 基因,三个在 NLRP3 基因。我们的研究结果表明,NLRP3 rs10754558 SNP 与巴西人群的 T1D 特异性相关(p = 4exp-3),NLRP3 rs358294199 SNP 与 CD 相关(p = 5exp-4)。尽管在挪威人群中与 T1D 强烈相关,但 NLRP1 与巴西人群的 T1D 无关。根据白种人群的先前研究,NLRP1 和 NLRP3 似乎与 AD 无关。由于已经报道 IL-1 beta 在免疫耐受丧失中具有全身作用,并且 NALP3 炎性小体直接参与这种促炎细胞因子的产生,我们假设 NLRP3 的变异可能属于导致自身免疫性疾病发展的易感性遗传背景。