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首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Antiplatelet factor 4/heparin antibodies in patients with gram negative bacteremia
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Antiplatelet factor 4/heparin antibodies in patients with gram negative bacteremia

机译:革兰氏阴性菌血症患者的抗血小板因子4 /肝素抗体

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Heparin-induced thrombocytopenia (HIT) is an antibody-mediated syndrome of thrombocytopenia and prothrombotic state that follows exposure to heparin. However, spontaneous HIT has been described in the setting of infection, without evidence of previous heparin administration. Since PF4 binds to lipid A portion of lipopolysaccharide, we tested for the presence of antiPF4/heparin antibodies in patients with gram-negative bacteremia. Patients with bacteremia had higher titers of antiPF4/heparin antibodies compared to normal controls 26.3 ± SD 34 units, N = 32 versus 6.3 ± SD 2.38 units, N = 10, P = 0.001. FITC-labeled PF4 interacted with lipopolysaccharide in a concentration-dependent manner as determined by quenching of the emission spectrum following excitation at λ 488. In addition, immunoaffinity purified antiPF4/Heparin antibodies from 3 patients with HIT cross-reacted with PF4/heparin complex. These results show that PF4/LPS complex is immunogenic and can elicit cross-reacting antibodies against PF4/Heparin, providing an explanation for the presence of these antibodies in individuals, who were never been exposed to heparin before. These antibodies may also be at least partly responsible for the thrombocytopenia associated with infection.
机译:肝素诱导的血小板减少症(HIT)是抗体介导的血小板减少症和血栓形成前状态的综合症,其暴露于肝素后。但是,自发性HIT已被描述为感染的情况,没有先前给予肝素的证据。由于PF4与脂多糖的脂质A部分结合,因此我们测试了革兰氏阴性菌血症患者中抗PF4 /肝素抗体的存在。与正常对照组相比,菌血症患者具有更高的抗PF4 /肝素抗体效价,分别为26.3±SD 34单位,N = 32和6.3±SD 2.38单位,N = 10,P = 0.001。 FITC标记的PF4与脂多糖以浓度依赖性方式相互作用,这是通过在λ488激发后猝灭发射光谱来确定的。此外,免疫亲和纯化的3例HIT患者的抗PF4 /肝素抗体与PF4 /肝素复合物发生了交叉反应。这些结果表明,PF4 / LPS复合物具有免疫原性,可以引发针对PF4 /肝素的交叉反应抗体,这为这些抗体在以前从未接触过肝素的个体中的存在提供了解释。这些抗体也可能至少部分负责与感染相关的血小板减少症。

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