Kjalke M, Johannessen M, Hedner U
Haemostasis Biology, Novo Nordisk A/S, Måløv, Denmark.
Semin Hematol. 2001 Oct;38(4 Suppl 12):15-20. doi: 10.1016/s0037-1963(01)90142-8.
Recombinant factor VIIa (rFVIIa; NovoSeven, Novo Nordisk, Copenhagen, Denmark) may help to promote hemostasis in patients with thrombocytopenia. We used two in vitro models of thrombin generation to evaluate this effect. The reconstituted model contained tissue factor (TF)-expressing monocytes, unactivated platelets, isolated plasma coagulation proteins, and calcium. Platelet activation and thrombin generation were measured in timed aliquots. In the plasma-based model, thrombin generation was measured continuously after the addition of lipidated TF and calcium to platelet-rich plasma using a slowly cleaved fluorescent substrate. Thrombocytopenic conditions were mimicked by decreasing the platelet density. In both systems, a platelet density-dependent lowering of the thrombin-generation peak was observed. Addition of rFVIIa to samples with low platelet density (6700 to 10000/microL) increased the initial thrombin generation in both systems without normalizing thrombin-generation curves. The magnitude of the rFVIIa effect was most pronounced in the plasma-based model. Platelet activation was not significantly delayed at low platelet density in the reconstituted model. Addition of rFVIIa to samples with low platelet density caused faster platelet activation, most likely as a consequence of the increased initial thrombin generation. The data suggest that rFVIIa may help to achieve hemostasis at low platelet densities by increasing the initial thrombin generation, thereby compensating for low platelet number.
重组凝血因子VIIa(rFVIIa;诺其,诺和诺德公司,丹麦哥本哈根)可能有助于促进血小板减少症患者的止血。我们使用了两种凝血酶生成的体外模型来评估这种作用。重组模型包含表达组织因子(TF)的单核细胞、未激活的血小板、分离的血浆凝血蛋白和钙。在定时取出的样品中测量血小板激活和凝血酶生成。在基于血浆的模型中,向富含血小板的血浆中加入脂化TF和钙后,使用缓慢裂解的荧光底物连续测量凝血酶生成。通过降低血小板密度模拟血小板减少的情况。在两个系统中,均观察到凝血酶生成峰值随血小板密度降低。向血小板密度低(6700至10000/微升)的样品中添加rFVIIa可增加两个系统中的初始凝血酶生成,但未使凝血酶生成曲线正常化。rFVIIa作用的幅度在基于血浆的模型中最为明显。在重组模型中,低血小板密度时血小板激活没有明显延迟。向低血小板密度的样品中添加rFVIIa导致血小板激活更快,这很可能是初始凝血酶生成增加的结果。数据表明,rFVIIa可能通过增加初始凝血酶生成来帮助在低血小板密度时实现止血,从而弥补血小板数量不足。