Lynch D M, Howe S E
Br J Haematol. 1986 Jun;63(2):301-8. doi: 10.1111/j.1365-2141.1986.tb05553.x.
Serum platelet bindable immunoglobulin (SPBIg) was determined in a group of 23 idiopathic thrombocytopenic purpura (ITP) patients and compared to 20 normal, healthy controls. The mean SPBIg of the ITP group was 16.1 (+/- 17.9 SD) fg/platelet, while the normals were substantially lower, 4.0 (+/- 1.2) fg/platelet. Sera from patients of both groups were then incubated with platelet fractions immobilized on nitrocellulose membrane strips (Western Blotting) to detect platelet antigen specificity using a peroxidase labelled indicator antibody. The normal patient sera did not react with platelet fractions on the nitrocellulose strips. However, 21 of 23 ITP sera bound to one or more platelet fractions with large variations in the number and molecular weights of the platelet fractions identified by ITP antibody. These observations suggest the presence of multiple antigenic binding sites for platelet specific immunoglobulin in ITP sera. This variation may reflect heterogeneous antibodies binding to diverse antigens or homogeneous antibodies to a limited number of antigenic determinants shared by several discrete platelet molecules.
测定了23例特发性血小板减少性紫癜(ITP)患者血清中的血小板可结合免疫球蛋白(SPBIg),并与20名正常健康对照者进行比较。ITP组的平均SPBIg为16.1(±17.9标准差)fg/血小板,而正常对照者则显著较低,为4.0(±1.2)fg/血小板。然后将两组患者的血清与固定在硝酸纤维素膜条上的血小板组分一起孵育(蛋白质印迹法),使用过氧化物酶标记的指示抗体检测血小板抗原特异性。正常患者血清与硝酸纤维素条上的血小板组分无反应。然而,23例ITP血清中有21例与一个或多个血小板组分结合,ITP抗体识别出的血小板组分在数量和分子量上有很大差异。这些观察结果表明ITP血清中存在针对血小板特异性免疫球蛋白的多个抗原结合位点。这种差异可能反映了异质性抗体与多种抗原结合,或同质性抗体与几种离散血小板分子共有的有限数量抗原决定簇结合。