Finke Doreen, Eloranta Maija-Leena, Rönnblom Lars
Section of Rheumatology, Department of Medical Sciences, Uppsala University, SE-75185, Uppsala, Sweden.
Autoimmunity. 2009 May;42(4):349-52. doi: 10.1080/08916930902831829.
Type I interferon (IFN) is produced by the innate immune system in several autoimmune diseases, such as systemic lupus erythematosus (SLE), polymyositis, and systemic sclerosis. In these diseases, immune complex (IC)-containing DNA or RNA may act as endogenous IFN inducers. The abilities of these IC to reach the endosomes in the plasmacytoid dendritic cells (PDC) cause the intracellular toll-like receptor (TLR) to initiate a cascade of transcription factors--a critical step in triggering type I IFN production. A special configuration of the nucleic acid (NA), such as CpG-rich non-methylated DNA or GU-rich RNA, appears crucial. However, other components of the IC, like HMGB1, may also be necessary. Studies regarding the genetic background of autoimmune diseases suggest that variants of genes involved in both IFN production and response are associated with disease susceptibility. This knowledge is important for the development of new therapeutic strategies in autoimmune diseases.
I型干扰素(IFN)由先天性免疫系统在几种自身免疫性疾病中产生,如系统性红斑狼疮(SLE)、多发性肌炎和系统性硬化症。在这些疾病中,含有免疫复合物(IC)的DNA或RNA可能作为内源性IFN诱导剂。这些IC到达浆细胞样树突状细胞(PDC)内体的能力会导致细胞内Toll样受体(TLR)启动一系列转录因子——这是触发I型IFN产生的关键步骤。核酸(NA)的特殊构型,如富含CpG的非甲基化DNA或富含GU的RNA,似乎至关重要。然而,IC的其他成分,如高迁移率族蛋白B1(HMGB1),可能也必不可少。关于自身免疫性疾病遗传背景的研究表明,参与IFN产生和反应的基因变体与疾病易感性相关。这一知识对于自身免疫性疾病新治疗策略的开发很重要。