Department of Dermatology, Second Xiangya Hospital, Central South University, Changsha, 410008, Hunan, People's Republic of China.
Hunan Key Laboratory of Medical Epigenomics, Second Xiangya Hospital, Central South University, Changsha, 410008, Hunan, People's Republic of China.
Clin Rev Allergy Immunol. 2020 Oct;59(2):248-272. doi: 10.1007/s12016-020-08798-2.
Type I interferons (IFN-Is) are a very important group of cytokines that are produced by innate immune cells but also act on adaptive immune cells. IFN-Is possess antiviral, antitumor, and anti-proliferative effects, as well are associated with the initiation and maintenance of autoimmune disorders. Studies have shown that aberrantly expressed IFN-Is and/or type I IFN-inducible gene signatures in the serum or tissues of patients with autoimmune disorders are linked to their pathogenesis, clinical manifestations, and disease activity. Type I interferonopathies with mutations in genes impacting the type I IFN signaling pathway have shown symptoms and characteristics similar to those of systemic lupus erythematosus (SLE). Furthermore, both interventions in animal models and clinical trials of therapies targeting the type I IFN signaling pathway have shown efficacy in the treatment of autoimmune diseases. Our review aims to summarize the functions and targeted therapies (as well as clinical trials) of IFN-Is in both adult and pediatric autoimmune diseases, such as SLE, pediatric SLE (pSLE), rheumatoid arthritis (RA), juvenile idiopathic arthritis (JIA), juvenile dermatomyositis (JDM), Sjögren syndrome (SjS), and systemic sclerosis (SSc), discussing the potential abnormal regulation of transcription factors and epigenetic modifications and providing a potential mechanism for pathogenesis and therapeutic strategies for future clinical use.
I 型干扰素 (IFN-Is) 是一类非常重要的细胞因子,它们由先天免疫细胞产生,但也作用于适应性免疫细胞。IFN-Is 具有抗病毒、抗肿瘤和抗增殖作用,与自身免疫疾病的发生和维持有关。研究表明,自身免疫疾病患者血清或组织中异常表达的 IFN-Is 和/或 I 型 IFN 诱导基因特征与疾病的发病机制、临床表现和疾病活动度有关。I 型干扰素病是由于影响 I 型 IFN 信号通路的基因突变引起的,其症状和特征与系统性红斑狼疮 (SLE) 相似。此外,针对 I 型 IFN 信号通路的动物模型干预和临床试验均表明,该通路的靶向治疗对自身免疫性疾病具有疗效。我们的综述旨在总结 IFN-Is 在成人和儿科自身免疫性疾病(如 SLE、儿科 SLE (pSLE)、类风湿关节炎 (RA)、幼年特发性关节炎 (JIA)、幼年皮肌炎 (JDM)、干燥综合征 (SjS) 和系统性硬化症 (SSc))中的作用和靶向治疗(以及临床试验),讨论转录因子和表观遗传修饰的潜在异常调节,并为未来的临床应用提供发病机制和治疗策略的潜在机制。