Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
Semin Hematol. 2013 Jul;50(3):e1-4. doi: 10.1053/j.seminhematol.2013.06.011.
Immune thrombocytopenia (ITP) is an autoimmune disorder characterized by increased platelet destruction or decreased platelet production. The mechanism of the disease has been extensively studied so that we now have a much improved understanding of the pathophysiology; however, the trigger of the autoimmunity remains unclear. More recently, oxidative stress was identified to be involved in the pathogenesis of ITP and provides a new hypothesis for the initiation of autoimmunity in patients with ITP. In this review, oxidative stress and its impact on autoimmunity, particularly ITP, will be covered.
免疫性血小板减少症 (ITP) 是一种自身免疫性疾病,其特征是血小板破坏增加或血小板生成减少。该疾病的发病机制已得到广泛研究,因此我们现在对其病理生理学有了更好的理解;然而,自身免疫的触发因素仍不清楚。最近,氧化应激被确定与 ITP 的发病机制有关,并为 ITP 患者自身免疫的发生提供了一个新的假说。在这篇综述中,将讨论氧化应激及其对自身免疫,特别是 ITP 的影响。