Kumagai Shunichi, Jikimoto Takumi, Saegusa Jun
Department of Biomedical Informatics, Graduate School of Medicine, Kobe University, Kobe 560-0017.
Rinsho Byori. 2003 Feb;51(2):126-32.
Autoimmune diseases are complex diseases in which both genetic and environmental factors are involved. Excessive oxidative stress is thought to have an important role in the pathogenesis of autoimmune diseases by enhancing the inflammation, inducing apoptotic cell death, and breaking down the immunological tolerance. When the state of oxidative stress was investigated in patients with rheumatoid arthritis(RA), systemic lupus erythematosus(SLE), and Sjögren's syndrome(SS) by oxidative stress profile(OSP), most subjects were in excessive oxidative stress or in defective antioxidant potentials. The thioredoxin(TRX) level in peripheral blood was significantly higher in these patients than in healthy subjects. Urinary excretion of 8-hydroxy-guanosine was also significantly increased in these patients compared with healthy subjects. We have proven that oxidative stress as well as UV irradiation induced the expression of SS-A/Ro52 autoantigen on the cell surface of keratinocytes. Oxidative stress not only injures the cellular components but also induces cellular responses, including apoptosis and gene activation. We also identified that GSTM1 null genotype was a candidate gene for susceptibility to SS and was associated with SS-A/Ro autoantibody production. In the synovial fluid of RA patients, TRX was abundantly detected and was produced in the lining layer of synovial tissue, indicating that TRX might protect synovial tissue from oxidative stress. Infections, UV irradiation, coldness, and emotional stress have been clinically well known as developing and exacerbating factors for autoimmune diseases. These environmental factors are closely related to oxidative stress. It is very important to develop reliable test methods to detect the state of oxidative stress and antioxidants.
自身免疫性疾病是涉及遗传和环境因素的复杂疾病。过量的氧化应激被认为通过增强炎症、诱导凋亡性细胞死亡以及破坏免疫耐受,在自身免疫性疾病的发病机制中起重要作用。当通过氧化应激谱(OSP)对类风湿性关节炎(RA)、系统性红斑狼疮(SLE)和干燥综合征(SS)患者的氧化应激状态进行调查时,大多数受试者处于过度氧化应激或抗氧化潜力缺陷状态。这些患者外周血中的硫氧还蛋白(TRX)水平明显高于健康受试者。与健康受试者相比,这些患者尿中8-羟基鸟苷的排泄也显著增加。我们已经证明,氧化应激以及紫外线照射可诱导角质形成细胞表面SS-A/Ro52自身抗原的表达。氧化应激不仅会损伤细胞成分,还会诱导包括细胞凋亡和基因激活在内的细胞反应。我们还确定GSTM1无效基因型是SS易感性的候选基因,并与SS-A/Ro自身抗体的产生有关。在RA患者的滑液中,大量检测到TRX,并且它在滑膜组织的衬里层中产生,这表明TRX可能保护滑膜组织免受氧化应激。感染、紫外线照射、寒冷和情绪应激在临床上一直被认为是自身免疫性疾病的发生和加重因素。这些环境因素与氧化应激密切相关。开发可靠的检测方法来检测氧化应激和抗氧化剂的状态非常重要。