Hymes K, Schur P H, Karpatkin S
Blood. 1980 Jul;56(1):84-7.
The gamma heavy-chain subclass of bound antiplatelet antibody was examined in six patients with autoimmune thrombocytopenic purpura (ATP) by a solid-phase radioimmunoassay. Monospecific antisera for gamma G1, gamma G2, gamma G3, and gamma G4 subclasses were employed in a "sandwich" technique, utilizing the binding of 126I-staphylococcal protein A. We have previously reported that serum antiplatelet antibody was restricted to be gamma G3 subclass in ATP. In contrast, all 4 IgG subclasses were found bound to platelets of ATP patients in the same distribution as that present in normal serum. It is suggested that the differences noted between serum antiplatelet IgG and platelet-bound IgG may represent different mechanisms of platelet injury.
通过固相放射免疫测定法检测了6例自身免疫性血小板减少性紫癜(ATP)患者体内结合抗血小板抗体的γ重链亚类。采用γG1、γG2、γG3和γG4亚类的单特异性抗血清,利用126I-葡萄球菌蛋白A的结合,以“夹心”技术进行检测。我们之前曾报道,ATP患者血清抗血小板抗体局限于γG3亚类。相比之下,在ATP患者的血小板上发现所有4种IgG亚类均有结合,其分布与正常血清中的相同。提示血清抗血小板IgG与血小板结合IgG之间的差异可能代表血小板损伤的不同机制。