Kelton J G, Smith J W, Warkentin T E, Hayward C P, Denomme G A, Horsewood P
Department of Medicine, McMaster University Medical Centre, Hamilton, Ontario, Canada.
Blood. 1994 Jun 1;83(11):3232-9.
Heparin-induced thrombocytopenia (HIT) is an important complication of heparin therapy. Although there is general agreement that platelet activation in vitro by the HIT IgG is mediated by the platelet Fc receptor, the interaction among the antibody, heparin, and platelet membrane components is uncertain and debated. In this report, we describe studies designed to address these interactions. We found, as others have noted, that a variety of other sulfated polysaccharides could substitute for heparin in the reaction. Using polysaccharides selected for both size and charge, we found that reactivity depended on two independent factors: a certain minimum degree of sulfation per saccharide unit and a certain minimum size. Hence, highly sulfated but small (< 1,000 daltons) polysaccharides were not reactive nor were large but poorly sulfated polysaccharides. The ability of HIT IgG to recognize heparin by itself was tested by Ouchterlony gel diffusion, ammonium sulfate and polyethylene glycol precipitation, and equilibrium dialysis. No technique demonstrated reactivity. However, when platelet releasate was added to heparin and HIT IgG, a 50-fold increase in binding of radio-labeled heparin to HIT IgG was observed. The releasate was then depleted of proteins capable of binding to heparin by immunoaffinity chromatography. Only platelet factor 4-immunodepleted releasate lost its reactivity with HIT IgG and heparin. Finally, to determine whether the reaction occurred on the surface of platelets or in the fluid phase, washed platelets were incubated with HIT IgG or heparin and after a wash step, heparin or HIT IgG was added, respectively. Reactivity was only noted when platelets were preincubated with heparin. Consistent with these observations was the demonstration of the presence of PF4 on platelets using flow cytometry. These studies indicate that heparin and other large, highly sulfated polysaccharides bind to PF4 to form a reactive antigen on the platelet surface. HIT IgG then binds to this complex with activation of platelets through the platelet Fc receptors.
肝素诱导的血小板减少症(HIT)是肝素治疗的一种重要并发症。尽管人们普遍认为,HIT IgG在体外对血小板的激活是由血小板Fc受体介导的,但抗体、肝素和血小板膜成分之间的相互作用尚不确定且存在争议。在本报告中,我们描述了旨在研究这些相互作用的实验。正如其他人所指出的,我们发现多种其他硫酸化多糖在该反应中可替代肝素。使用根据大小和电荷选择的多糖,我们发现反应活性取决于两个独立因素:每个糖单位一定的最小硫酸化程度和一定的最小大小。因此,高度硫酸化但小的(<1000道尔顿)多糖无反应性,大的但硫酸化程度低的多糖也无反应性。通过欧氏凝胶扩散、硫酸铵和聚乙二醇沉淀以及平衡透析测试了HIT IgG自身识别肝素的能力。没有技术显示出反应性。然而,当将血小板释放物添加到肝素和HIT IgG中时,观察到放射性标记的肝素与HIT IgG的结合增加了50倍。然后通过免疫亲和色谱法去除释放物中能够与肝素结合的蛋白质。只有血小板因子4免疫去除的释放物失去了与HIT IgG和肝素的反应性。最后,为了确定反应是发生在血小板表面还是液相中,将洗涤后的血小板与HIT IgG或肝素孵育,经过洗涤步骤后,分别添加肝素或HIT IgG。只有当血小板预先与肝素孵育时才观察到反应性。使用流式细胞术证明血小板上存在PF4与这些观察结果一致。这些研究表明,肝素和其他大的、高度硫酸化的多糖与PF4结合,在血小板表面形成一种反应性抗原。然后,HIT IgG通过血小板Fc受体与该复合物结合并激活血小板。