Iwamoto Taro, Niewold Timothy B
Division of Rheumatology & Department of Immunology, Mayo Clinic, Rochester, MN 55905, USA.
Division of Rheumatology & Department of Immunology, Mayo Clinic, Rochester, MN 55905, USA.
Clin Immunol. 2017 Dec;185:32-39. doi: 10.1016/j.clim.2016.09.012. Epub 2016 Sep 28.
Systemic lupus erythematosus (SLE) is an inflammatory autoimmune disease characterized by immune complex formation with multi-organ manifestations. Lupus nephritis (LN) is one of the most severe types of organ damage in SLE, and it clearly contributes to increased morbidity and mortality due to SLE. LN occurs more frequently and is more severe in non-European ancestral backgrounds, although the cause of this disparity remains largely unknown. Genetic factors play an important role in the pathogenesis of SLE. Although many SLE susceptibility genes have been identified, the genetic basis of LN is not as well understood. While some of the established general SLE susceptibility genes are associated with LN, recent discoveries highlight a number of genes with renal functions that are specifically associated with LN. Some of these genes associated with LN help to explain the disparity in the prevalence of nephritis between individuals with SLE, and also partially explain differences in LN between ancestral backgrounds. Moreover, not only the gene mutations, but also post-translational modifications seem to play important roles in the pathogenesis of LN. Overall it seems likely that a combination of general SLE susceptibility genes cooperate with LN specific risk genes to result in the genetic propensity for LN. In this review, we will outline the genetic contribution to LN and describe possible roles of LN susceptibility genes.
系统性红斑狼疮(SLE)是一种炎症性自身免疫性疾病,其特征是形成免疫复合物并伴有多器官表现。狼疮性肾炎(LN)是SLE中最严重的器官损伤类型之一,它显然导致了SLE发病率和死亡率的增加。LN在非欧洲祖先背景中更频繁发生且更严重,尽管这种差异的原因在很大程度上仍不清楚。遗传因素在SLE的发病机制中起重要作用。虽然已经鉴定出许多SLE易感基因,但LN的遗传基础尚未得到很好的理解。虽然一些已确定的一般SLE易感基因与LN有关,但最近的发现突出了一些具有肾脏功能的基因,这些基因与LN特异性相关。其中一些与LN相关的基因有助于解释SLE患者之间肾炎患病率的差异,也部分解释了不同祖先背景之间LN的差异。此外,不仅基因突变,而且翻译后修饰似乎在LN的发病机制中也起重要作用。总体而言,一般SLE易感基因与LN特异性风险基因的组合似乎可能导致LN的遗传倾向。在本综述中,我们将概述遗传对LN的贡献,并描述LN易感基因的可能作用。