Wegert W, Harder S, Bassus S, Kirchmaier C M
Institute for Clinical Pharmacology, Pharmazentrum Frankfurt, University Hospital Frankfurt am Main, Germany.
Platelets. 2005 Feb;16(1):45-50. doi: 10.1080/09537100400008059.
Although the administration of recombinant coagulation factor VIIa (rFVIIa) is a well established treatment in haemophilia with inhibitory antibodies, monitoring the therapeutic efficacy is still a problem. This is because the complete haemostatic effect in vivo depends on negatively charged surfaces provided by exposed lipids from activated platelets which are not present in standard clinical assays using plasma. The thrombin generation assay, however, measures the endogenous thrombin potential (ETP) in platelet-rich plasma (PRP) and this assay might be useful for monitoring the haemostatic response to rFVIIa. We characterized the in vitro concentration-response relationship of rFVIIa and the thrombin generation parameters ETP, PEAK and TIME TO PEAK using platelet-rich plasma (PRP) and rFVIIa at concentrations between one and five times the therapeutic dose. We also studied the effect of inhibiting tissue-factor and the intrinsic coagulation pathway using excess TF-neutralizing antibodies and corn trypsin inhibitor (CTI), respectively. There was a sigmoid relationship between ETP and PEAK and the dose of rFVIIa. Increasing rFVIIa concentrations between 100 and 500 U/ml resulted in a progressive increase in ETP, whereas supratherapeutical concentrations led to a plateau phase. The plateau phase differed between patients, suggesting a biological variation in the maximum ETP. Neutralization of plasma TF with TF-Ab partially decreased FVIIa efficacy. The inhibitory effect of CTI on rFVIIa-induced thrombin generation via the intrinsic pathway was negligible. The thrombin generation assay using PRP is a useful test for determining the sufficient efficacy of rFVIIa in blood. Once a plateau level is reached, higher doses of rFVIIa have no additional effect on haemostatic efficacy. The variation in plateau levels between subjects indicates that there are inter-individual differences in the level of thrombin activity that can be generated. High doses of rFVIIa are effective even in the absence of TF.
尽管重组凝血因子VIIa(rFVIIa)的给药在伴有抑制性抗体的血友病治疗中已成为一种成熟的疗法,但监测其治疗效果仍是一个问题。这是因为体内完整的止血效应取决于活化血小板暴露的脂质提供的带负电荷表面,而这在使用血浆的标准临床检测中并不存在。然而,凝血酶生成检测可测量富血小板血浆(PRP)中的内源性凝血酶潜力(ETP),该检测可能有助于监测对rFVIIa的止血反应。我们使用富血小板血浆(PRP)和浓度为治疗剂量1至5倍的rFVIIa,对rFVIIa与凝血酶生成参数ETP、峰值和达到峰值时间之间的体外浓度-反应关系进行了表征。我们还分别使用过量的TF中和抗体和玉米胰蛋白酶抑制剂(CTI)研究了抑制组织因子和内源性凝血途径的效果。ETP、峰值与rFVIIa剂量之间呈S形关系。rFVIIa浓度在100至500 U/ml之间增加时,ETP逐渐升高,而超治疗浓度则导致平台期。不同患者的平台期有所不同,表明最大ETP存在生物学差异。用TF-Ab中和血浆TF可部分降低FVIIa疗效。CTI对rFVIIa通过内源性途径诱导的凝血酶生成的抑制作用可忽略不计。使用PRP进行的凝血酶生成检测是确定rFVIIa在血液中充分疗效的有用试验。一旦达到平台水平,更高剂量的rFVIIa对止血疗效没有额外影响。个体间平台水平的差异表明,可产生的凝血酶活性水平存在个体差异。即使在没有TF的情况下,高剂量的rFVIIa也有效。