Department of Dermatology, Mersin University, Mersin, Turkey.
Tehran University of Medical Sciences, Tehran, Iran.
Adv Exp Med Biol. 2022;1367:259-298. doi: 10.1007/978-3-030-92616-8_10.
Systemic sclerosis (SSc) is a rare disease with a prevalence ranging from 7 to 700 cases per million. Like with most autoimmune diseases, both environmental and genetic factors are involved in the pathogenesis of the SSc. Though the incidence of SSc in the family members of those affected and the concordance rate in twins is very low, inheritance is still the strongest risk factor of SSc. Thus, multiple studies have been conducted to identify the genes responsible for this inheritance including candidate gene association studies and genome-wide analyses. Variations and mutations in the genes encoding cytokines, adhesion molecules, and signaling proteins involved in the interaction between endothelial cells, fibroblasts, and immune cells have been found to be associated with SSc susceptibility. In this chapter, these genes and their contribution to the pathogenesis of the SSc are discussed in detail. These genes are categorized into five major groups of HLA genes, genes involved in the innate immune responses, genes affecting adaptive immune responses, genes with a role in the fibrogenesis pathways, and apoptosis, autophagy, and pyroptosis-related genes.
系统性硬化症(SSc)是一种罕见疾病,其患病率为每百万人口中有 7 至 700 例。与大多数自身免疫性疾病一样,SSc 的发病机制涉及环境和遗传因素。尽管受影响者的家庭成员中的 SSc 发病率和双胞胎的一致性率非常低,但遗传仍然是 SSc 的最强风险因素。因此,已经进行了多项研究来确定与这种遗传相关的基因,包括候选基因关联研究和全基因组分析。已发现编码细胞因子、黏附分子和信号蛋白的基因中的变异和突变与 SSc 的易感性相关,这些基因参与内皮细胞、成纤维细胞和免疫细胞之间的相互作用。在本章中,详细讨论了这些基因及其对 SSc 发病机制的贡献。这些基因分为五个主要组:HLA 基因、参与固有免疫反应的基因、影响适应性免疫反应的基因、在纤维化途径中起作用的基因以及与细胞凋亡、自噬和细胞焦亡相关的基因。