Department of Pediatrics, Division of Hematology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Blood. 2011 Jan 6;117(1):290-8. doi: 10.1182/blood-2010-08-300756. Epub 2010 Sep 23.
Inhibitory antibodies to factors VIII or IX represent a serious complication for hemophilia patients. Treatment involves products that bypass the intrinsic pathway and promote thrombin generation. Direct infusion of factor Xa should also restore hemostasis; however, it has a short half-life in plasma and could activate systemic coagulation in an uncontrolled fashion. Here we show that factor Xa mutants with zymogen-like properties (FXa(I16L) and FXa(V17A)) circumvent these limitations. In the absence of factor Va, the FXa variants are poor enzymes for a range of physiological ligands and are resistant to inactivation by antithrombin III and tissue factor pathway inhibitor. Notably, assembly of FXa(I16L) and FXa(V17A) on activated platelets with factor Va to form prothrombinase completely restores biologic activity. In hemophilic plasma, FXa(I16L) and FXa(V17A) have prolonged half-lives compared with wild-type factor Xa (approximately 60 minutes vs approximately 1 minute) and promote robust thrombin generation that bypasses the intrinsic pathway. The variants require factor Va generated in situ for procoagulant function, and cofactor inactivation by the protein C pathway regulates their activity. The efficacy, extended half-life, and mechanism of action suggest that novel zymogen-like forms of factor Xa might prove useful as new therapeutic procoagulants to treat deficiencies upstream of the common pathway.
抑制物抗体对因子 VIII 或 IX 的影响是血友病患者的严重并发症。治疗方法涉及绕过固有途径并促进凝血酶生成的产品。直接输注因子 Xa 也应该恢复止血;然而,它在血浆中的半衰期很短,并且可能以不受控制的方式激活全身凝血。在这里,我们展示了具有酶原样特性的因子 Xa 突变体(FXa(I16L) 和 FXa(V17A))克服了这些限制。在没有因子 Va 的情况下,这些 FXa 变体对于一系列生理配体来说是低效的酶,并且对抗凝血酶 III 和组织因子途径抑制剂的失活具有抗性。值得注意的是,FXa(I16L) 和 FXa(V17A) 与活化血小板上的因子 Va 组装形成凝血酶原酶完全恢复了生物学活性。在血友病血浆中,与野生型因子 Xa 相比,FXa(I16L) 和 FXa(V17A) 的半衰期延长(约 60 分钟与约 1 分钟),并促进绕过固有途径的强烈凝血酶生成。这些变体需要原位生成的因子 Va 发挥促凝功能,并且蛋白 C 途径的辅因子失活调节其活性。功效、延长的半衰期和作用机制表明,新型酶原样形式的因子 Xa 可能作为新的治疗性促凝血剂用于治疗共同途径上游的缺乏症。