Tomiyama Y, Take H, Kosugi S, Kashiwagi H, Kanayama Y, Kurata Y, Matsuzawa Y
Second Department of Internal Medicine, Osaka University Medical School.
Rinsho Ketsueki. 1993 Jan;34(1):21-7.
This study was designed to investigate the pathogenic relevance of platelet-associated autoantibodies in chronic ITP, since the titer of platelet-associated autoantibodies does not appear to correlate with the severity of the disease. Employing a direct immunoprecipitation procedure, we examined platelets from three ITP patients with platelet-associated autoantibodies against GPIIb-IIIa and an unidentified 56 kD protein before and after splenectomy. In two patients, platelet-associated autoantibodies disappeared after splenectomy, and these two patients attained complete remission. In one patient, however, the amount of platelet-associated autoantibodies did not decrease after splenectomy. Although this patient's platelet count transiently increased to 500 x 10(3)/microliters after splenectomy, it decreased to 55 x 10(3)/microliters within a short time. These findings suggest that platelet-associated autoantibodies play a key role in platelet destruction in chronic ITP.
本研究旨在探讨血小板相关自身抗体在慢性免疫性血小板减少性紫癜(ITP)中的致病相关性,因为血小板相关自身抗体的滴度似乎与疾病的严重程度无关。采用直接免疫沉淀法,我们检测了3例ITP患者脾切除前后针对糖蛋白IIb-IIIa和一种未鉴定的56kD蛋白的血小板相关自身抗体。2例患者脾切除后血小板相关自身抗体消失,这2例患者获得完全缓解。然而,1例患者脾切除后血小板相关自身抗体量未减少。尽管该患者脾切除后血小板计数短暂升至500×10³/微升,但短时间内又降至55×10³/微升。这些发现提示血小板相关自身抗体在慢性ITP的血小板破坏中起关键作用。