Reilly M P, Taylor S M, Franklin C, Sachais B S, Cines D B, Williams K J, McKenzie S E
Cardeza Foundation for Hematologic Research, Thomas Jefferson University, Philadelphia, PA 19107, USA.
J Thromb Haemost. 2006 Dec;4(12):2687-94. doi: 10.1111/j.1538-7836.2006.02201.x. Epub 2006 Sep 8.
Heparin-induced thrombocytopenia/thrombosis (HIT/T) is a common cause of life- and limb-threatening thrombosis. The development of antibodies that react with complexes of heparin and platelet factor 4 (PF4) is fundamental to the development of the disease. However, anti-PF4/heparin antibodies are far more common than is HIT/T and there is less understanding of the factors that contribute to thrombosis in only a subset of patients.
Both qualitative and quantitative differences in multiple factors (e.g. antibodies, heparin and platelets) may influence the clinical course of patients who develop anti-PF4/heparin antibodies. We examined the hypothesis that host-specific factors, such as comorbid prothrombotic conditions, would exacerbate the pathologic effects of anti-PF4/heparin antibodies.
A mouse model transgenic for human Fcgamma RIIa and PF4 and null for mouse PF4 was used to study the influence of prothrombotic conditions on the effects of anti-PF4/heparin antibodies in vivo. To simulate a prothrombotic milieu, mice were fed a hypercholesterolemic diet (HD). HD-fed mice had elevated plasma cholesterol, increased platelet reactivity and increased endothelial activation relative to mice fed a standard diet (SD). Age- and sex-matched mice from each diet group were treated with an anti-PF4/heparin antibody and heparin. HD-fed mice developed more severe thrombocytopenia than similarly treated SD-fed mice. Mice with moderate to severe thrombocytopenia had elevated plasma levels of thrombin-antithrombin complexes, indicative of increased thrombin generation in vivo. Platelet-fibrin thrombi were observed in multiple organs of HD-fed mice that developed severe thrombocytopenia.
Host-specific factors, such as prothrombotic changes in platelet reactivity and/or endothelial activation, may influence the development of thrombosis in a subset of patients who develop anti-PF4/heparin antibodies.
肝素诱导的血小板减少症/血栓形成(HIT/T)是危及生命和肢体的血栓形成的常见原因。与肝素和血小板因子4(PF4)复合物发生反应的抗体的产生是该疾病发生的基础。然而,抗PF4/肝素抗体远比HIT/T常见,对于仅在一部分患者中导致血栓形成的因素了解较少。
多种因素(如抗体、肝素和血小板)在质量和数量上的差异可能会影响产生抗PF4/肝素抗体患者的临床病程。我们检验了如下假设:宿主特异性因素,如合并的血栓前状态,会加剧抗PF4/肝素抗体的病理作用。
利用一种转基因小鼠模型来研究血栓前状态对体内抗PF4/肝素抗体作用的影响,该模型中人FcγRIIa和PF4呈转基因状态,而小鼠PF4呈无效状态。为模拟血栓前环境,给小鼠喂食高胆固醇饮食(HD)。与喂食标准饮食(SD)的小鼠相比,喂食HD的小鼠血浆胆固醇升高、血小板反应性增加且内皮激活增强。每个饮食组中年龄和性别匹配的小鼠用抗PF4/肝素抗体和肝素进行治疗。与同样处理的喂食SD的小鼠相比,喂食HD的小鼠发生了更严重的血小板减少症。中度至重度血小板减少症的小鼠血浆凝血酶-抗凝血酶复合物水平升高,表明体内凝血酶生成增加。在发生严重血小板减少症的喂食HD的小鼠的多个器官中观察到血小板-纤维蛋白血栓。
宿主特异性因素,如血小板反应性和/或内皮激活方面的血栓前变化,可能会影响一部分产生抗PF4/肝素抗体患者的血栓形成发展。