Postgraduate Program in Genetics, Department of Genetics, Federal University of Paraná, Curitiba, Brazil.
Lübeck Institute of Experimental Dermatology, University of Lübeck, Lübeck, Germany.
Exp Dermatol. 2021 Jun;30(6):831-840. doi: 10.1111/exd.14275. Epub 2021 Jan 15.
Pemphigus foliaceus (PF) is an autoimmune blistering disease of the skin, clinically characterized by erosions and, histopathologically, by acantholysis. PF is endemic in the Brazilian Central-Western region. Numerous single nucleotide polymorphisms (SNPs) have been shown to affect the susceptibility for PF, including SNPs at long non-coding RNA (lncRNA) genes, which are known to participate in many physiological and pathogenic processes, such as autoimmunity. Here, we investigated whether the genetic variation of immune-related lncRNA genes affects the risk for endemic and sporadic forms of PF. We analysed 692 novel SNPs for PF from 135 immune-related lncRNA genes in 227 endemic PF patients and 194 controls. The SNPs were genotyped by Illumina microarray and analysed by applying logistic regression at additive model, with correction for sex and population structure. Six associated SNPs were also evaluated in an independent German cohort of 76 sporadic PF patients and 150 controls. Further, we measured the expression levels of two associated lncRNA genes (LINC-PINT and LY86-AS1) by quantitative PCR, stratified by genotypes, in peripheral blood mononuclear cells of healthy subjects. We found 27 SNPs in 11 lncRNA genes associated with endemic PF (p < .05 without overlapping with protein-coding genes). Among them, the LINC-PINT SNP rs10228040A (OR = 1.47, p = .012) was also associated with increased susceptibility for sporadic PF (OR = 2.28, p = .002). Moreover, the A+ carriers of LY86-AS1rs12192707 mark lowest LY86-AS1 RNA levels, which might be associated with a decreasing autoimmune response. Our results suggest a critical role of lncRNA variants in immunopathogenesis of both PF endemic and sporadic forms.
落叶型天疱疮(PF)是一种皮肤自身免疫性水疱病,临床上表现为糜烂,组织病理学上表现为棘层松解。PF 在巴西中西部地区流行。大量单核苷酸多态性(SNP)已被证明与 PF 的易感性相关,包括长非编码 RNA(lncRNA)基因的 SNP,这些基因已知参与许多生理和病理过程,如自身免疫。在这里,我们研究了免疫相关 lncRNA 基因的遗传变异是否影响地方性和散发性 PF 的风险。我们分析了来自 135 个免疫相关 lncRNA 基因的 227 名地方性 PF 患者和 194 名对照的 692 个新型 SNP 与 PF 的相关性。通过 Illumina 微阵列对 SNP 进行基因分型,并应用 logistic 回归分析加性模型,校正性别和人群结构。还在一个独立的德国散发性 PF 患者和 150 名对照的队列中评估了 6 个相关 SNP。此外,我们还通过定量 PCR,根据基因型,在健康受试者的外周血单核细胞中测量了两个相关 lncRNA 基因(LINC-PINT 和 LY86-AS1)的表达水平。我们在 11 个 lncRNA 基因中发现了 27 个与地方性 PF 相关的 SNP(p<.05,与蛋白质编码基因无重叠)。其中,LINC-PINT SNP rs10228040A(OR=1.47,p=0.012)也与散发性 PF 的易感性增加相关(OR=2.28,p=0.002)。此外,LY86-AS1rs12192707 的 A+携带者的 LY86-AS1 RNA 水平最低,这可能与自身免疫反应减弱有关。我们的研究结果表明,lncRNA 变异在地方性和散发性 PF 的免疫发病机制中起关键作用。