Sestan Mario, Kifer Nastasia, Arsov Todor, Cook Matthew, Ellyard Julia, Vinuesa Carola G, Jelusic Marija
Department of Paediatrics, University of Zagreb School of Medicine, University Hospital Centre Zagreb, 10000 Zagreb, Croatia.
Faculty of Medical Sciences, University Goce Delchev, 2000 Shtip, North Macedonia.
Curr Issues Mol Biol. 2023 Jul 17;45(7):5981-6002. doi: 10.3390/cimb45070378.
The pathogenesis of childhood-onset systemic lupus erythematosus (cSLE) is complex and not fully understood. It involves three key factors: genetic risk factors, epigenetic mechanisms, and environmental triggers. Genetic factors play a significant role in the development of the disease, particularly in younger individuals. While cSLE has traditionally been considered a polygenic disease, it is now recognized that in rare cases, a single gene mutation can lead to the disease. Although these cases are uncommon, they provide valuable insights into the disease mechanism, enhance our understanding of pathogenesis and immune tolerance, and facilitate the development of targeted treatment strategies. This review aims to provide a comprehensive overview of both monogenic and polygenic SLE, emphasizing the implications of specific genes in disease pathogenesis. By conducting a thorough analysis of the genetic factors involved in SLE, we can improve our understanding of the underlying mechanisms of the disease. Furthermore, this knowledge may contribute to the identification of effective biomarkers and the selection of appropriate therapies for individuals with SLE.
儿童期系统性红斑狼疮(cSLE)的发病机制复杂,尚未完全明确。它涉及三个关键因素:遗传风险因素、表观遗传机制和环境触发因素。遗传因素在该疾病的发生发展中起着重要作用,尤其是在较年轻的个体中。虽然传统上认为cSLE是一种多基因疾病,但现在人们认识到,在罕见情况下,单个基因突变也可导致该病。尽管这些病例并不常见,但它们为疾病机制提供了有价值的见解,增进了我们对发病机制和免疫耐受的理解,并有助于制定靶向治疗策略。本综述旨在全面概述单基因和多基因SLE,强调特定基因在疾病发病机制中的意义。通过对SLE所涉及的遗传因素进行深入分析,我们可以更好地理解该疾病的潜在机制。此外,这些知识可能有助于识别有效的生物标志物,并为SLE患者选择合适的治疗方法。