McMillan R, Martin M, Bakich M J, Morrison J
Immunopharmacology. 1979 Mar;1(2):83-7. doi: 10.1016/0162-3109(79)90045-6.
A new approach to the study of antiplatelet antibodies is described. Purified IgG from sera or from the culture of splenic ells was radiolabeled with 125I. Incubation of radiolabeled splenic IgG from ITP patients showed significantly greater binding to target platelets when compared to control IgG samples; conversely, the binding to target platelets of 125I-labeled serum IgG from ITP patients did not differ from controls. In each of the six instances when the binding of splenic and serum IgG from the same ITP patients was compared, the splenic samples contained a much higher concentration of platelet-specific IgG. This suggests that intrasplenic platelets in ITP patients are exposed in vivo to high concentrations of antiplatelet antibody and may explain, in part, the importance of the spleen in platelet destruction in this disease. This assay should prove useful in the further study of immune thrombocytopenia.
本文描述了一种研究抗血小板抗体的新方法。从血清或脾细胞培养物中纯化的IgG用125I进行放射性标记。与对照IgG样本相比,ITP患者放射性标记的脾IgG与靶血小板的结合明显更强;相反,ITP患者125I标记的血清IgG与靶血小板的结合与对照无差异。在比较同一ITP患者脾IgG和血清IgG结合的六个实例中,脾样本中血小板特异性IgG的浓度要高得多。这表明ITP患者脾内的血小板在体内暴露于高浓度的抗血小板抗体,这可能部分解释了脾脏在该疾病血小板破坏中的重要性。该检测方法在免疫性血小板减少症的进一步研究中应会被证明有用。