Lee A Y Y, Vlasuk G P
Department of Medicine, McMaster University, Hamilton, ON, Canada.
J Intern Med. 2003 Oct;254(4):313-21. doi: 10.1046/j.1365-2796.2003.01224.x.
Originally isolated from a haematophagous hookworm, recombinant nematode anticoagulant protein c2 (rNAPc2) is an 85-amino acid protein with potent anticoagulant properties. Unlike conventional anticoagulants that attenuate blood coagulation via inhibition of thrombin or activated factor X (FXa) at the downstream portion of the cascade, rNAPc2 is a potent inhibitor of the activated factor VII/tissue factor complex (FVIIa/TF), the key physiological initiator of blood coagulation. Its mechanism of action requires prerequisite binding to circulating FXa or zymogen factor X (FX) to form a binary complex prior to its interaction and inhibition of membrane-bound FVIIa/TF. The binding of rNAPc2 to FX results in an elimination half-life of longer than 50 h following either subcutaneous or intravenous administration. Recombinant NAPc2, like other inhibitors of FVIIa/TF including tissue factor pathway inhibitor (TFPI) and active site-blocked FVIIa (ASIS, FFR-rFVIIa or FVIIai), may have a promising role in the prevention and treatment of venous and arterial thrombosis, as well as potential efficacy in the management of disseminated intravascular coagulopathies because of their potent and selective inhibition of FVIIa/TF.
重组线虫抗凝血蛋白c2(rNAPc2)最初是从一种吸血钩虫中分离出来的,它是一种具有85个氨基酸的蛋白质,具有强大的抗凝血特性。与通过在凝血级联下游抑制凝血酶或活化因子X(FXa)来减弱血液凝固的传统抗凝血剂不同,rNAPc2是活化因子VII/组织因子复合物(FVIIa/TF)的强效抑制剂,而FVIIa/TF是血液凝固的关键生理启动因子。其作用机制要求在与膜结合的FVIIa/TF相互作用并抑制之前,先与循环中的FXa或X因子酶原(FX)结合形成二元复合物。皮下或静脉注射后,rNAPc2与FX的结合导致消除半衰期超过50小时。重组NAPc2与其他FVIIa/TF抑制剂一样,包括组织因子途径抑制剂(TFPI)和活性位点阻断的FVIIa(ASIS、FFR-rFVIIa或FVIIai),由于它们对FVIIa/TF具有强大而选择性的抑制作用,可能在预防和治疗静脉和动脉血栓形成方面发挥有前景的作用,以及在管理弥散性血管内凝血方面具有潜在疗效。