Tomiyama Yoshiaki, Kosugi Satoru
Department of Hematology and Oncology, Graduate School of Medicine C9, Osaka University, Suita, Japan.
Int J Hematol. 2005 Feb;81(2):100-5. doi: 10.1532/ijh97.04193.
Chronic immune thrombocytopenic purpura (ITP) is an autoimmune disorder characterized by early platelet destruction mediated by antiplatelet autoantibodies. Platelet membrane glycoproteins (GP), especially GPIIb-IIIa and GPIb-IX, contain major autoantigenic determinants in chronic ITP. Recent advances in the localization of autoantigens as well as in the detection of GP-specific antibodies have improved our understanding of the pathophysiology of the disease. The N-terminal globular head of GPIIb-IIIa, particularly the beta-propeller domain in GPIIb, seems to play an important role as a hot spot for autoantigenic epitopes in chronic ITP.
慢性免疫性血小板减少性紫癜(ITP)是一种自身免疫性疾病,其特征是由抗血小板自身抗体介导的早期血小板破坏。血小板膜糖蛋白(GP),尤其是GPIIb-IIIa和GPIb-IX,是慢性ITP中的主要自身抗原决定簇。自身抗原定位以及GP特异性抗体检测方面的最新进展,增进了我们对该疾病病理生理学的理解。GPIIb-IIIa的N端球状头部,特别是GPIIb中的β-螺旋桨结构域,似乎作为慢性ITP中自身抗原表位的热点发挥着重要作用。