Hedner U, Erhardtsen E
Wallenberg Laboratory, University Hospital Malmö, University of Lund, Sweden.
Ann Med. 2000 Dec;32 Suppl 1:68-72.
Following vessel wall injury, tissue factor (TF) is being exposed and forms complexes with the already activated FVII (FVIIa) present in the circulating blood, providing a limited amount of thrombin molecules that activate a number of coagulation proteins as well as the platelets. As a result of activation with thrombin the platelet surface exposes negatively charged phospholipids to which activated coagulation proteins bind tightly, and full thrombin generation occurs, resulting in the conversion of fibrinogen into fibrin. After the first FXa is formed, the tissue factor pathway inhibitor (TFPI) forms a complex with FXa. In the next step a quaternary complex is being formed, TF/FVIIa/FXa/TFPI, which inhibits the first step of the haemostatic pathway. Recombinant FVIIa (rFVIIa) has been developed for use as a haemostatic agent (NovoNordisk A/S, Denmark). Inactivated rFVIIa (rFVIIai) has also been prepared, and it has similar binding capacity to TF as rFVIIa but it blocks the catalytic activity of the TF complex. In various animal models rFVIIai has been demonstrated to prevent or diminish immediate thrombus formation at the site of vessel wall injury (athroplasty or other forms of mechanical injury) as well as the development of long-term intima thickening. Also, topical application of rFVIIai was found to block the formation of a thrombus. rFVIIai was shown to have an anti-inflammatory effect in lipopolysaccharide (LPS)-induced sepsis, and postischaemic reperfusion injury was found to be reduced by the administration of rFVIIai. In a limited number of patients undergoing percutaneous transluminal coronary angioplasty (PTCA), rFVIIai was observed to allow PTCA to be performed at lower doses of heparin than what has been reported previously. Recombinant TFPI has been shown to attenuate the lethal inflammatory and coagulopathic response. Furthermore, topical application of rFVIIai has been found to increase the patency rate in a model of graft surgery.
血管壁损伤后,组织因子(TF)暴露,并与循环血液中已激活的FVII(FVIIa)形成复合物,产生少量凝血酶分子,这些分子可激活多种凝血蛋白以及血小板。由于凝血酶的激活,血小板表面暴露出带负电荷的磷脂,激活的凝血蛋白与之紧密结合,从而产生足量的凝血酶,导致纤维蛋白原转化为纤维蛋白。首个FXa形成后,组织因子途径抑制剂(TFPI)与FXa形成复合物。接下来形成四元复合物TF/FVIIa/FXa/TFPI,它会抑制止血途径的第一步。重组FVIIa(rFVIIa)已被开发用作止血剂(丹麦诺和诺德公司)。也制备了灭活的rFVIIa(rFVIIai),它与rFVIIa具有相似的与TF结合的能力,但会阻断TF复合物的催化活性。在各种动物模型中,已证明rFVIIai可预防或减少血管壁损伤部位(血管成形术或其他形式的机械损伤)的即时血栓形成以及长期内膜增厚的发展。此外,发现局部应用rFVIIai可阻断血栓形成。rFVIIai在脂多糖(LPS)诱导的脓毒症中显示出抗炎作用,并且发现给予rFVIIai可减轻缺血后再灌注损伤。在少数接受经皮冠状动脉腔内血管成形术(PTCA)的患者中,观察到rFVIIai可使PTCA在比先前报道的更低剂量的肝素下进行。重组TFPI已显示可减轻致命的炎症和凝血病反应。此外,发现在移植手术模型中局部应用rFVIIai可提高通畅率。