Division of Cardiovascular & Diabetes Research, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM), University of Leeds, Leeds LS2 9JT, UK.
Int J Mol Sci. 2021 Nov 21;22(22):12537. doi: 10.3390/ijms222212537.
Thrombus formation remains a major cause of morbidity and mortality worldwide. Current antiplatelet and anticoagulant therapies have been effective at reducing vascular events, but at the expense of increased bleeding risk. Targeting proteins that interact with fibrinogen and which are involved in hypofibrinolysis represents a more specific approach for the development of effective and safe therapeutic agents. The antifibrinolytic proteins alpha-2 antiplasmin (α2AP), thrombin activatable fibrinolysis inhibitor (TAFI), complement C3 and plasminogen activator inhibitor-2 (PAI-2), can be incorporated into the fibrin clot by FXIIIa and affect fibrinolysis by different mechanisms. Therefore, these antifibrinolytic proteins are attractive targets for the development of novel therapeutics, both for the modulation of thrombosis risk, but also for potentially improving clot instability in bleeding disorders. This review summarises the main properties of fibrinogen-bound antifibrinolytic proteins, their effect on clot lysis and association with thrombotic or bleeding conditions. The role of these proteins in therapeutic strategies targeting the fibrinolytic system for thrombotic diseases or bleeding disorders is also discussed.
血栓形成仍然是全世界发病率和死亡率的主要原因。目前的抗血小板和抗凝治疗在降低血管事件方面是有效的,但代价是出血风险增加。针对与纤维蛋白原相互作用并参与低纤维蛋白溶解的蛋白质,代表了开发有效和安全治疗药物的更具体方法。纤维蛋白结合的抗纤维蛋白溶酶蛋白 α2 抗纤溶酶 (α2AP)、凝血酶激活的纤维蛋白溶解抑制剂 (TAFI)、补体 C3 和纤溶酶原激活物抑制剂-2 (PAI-2),可以通过 FXIIIa 掺入纤维蛋白凝块,并通过不同的机制影响纤维蛋白溶解。因此,这些抗纤维蛋白溶酶蛋白是开发新型治疗药物的有吸引力的靶点,既可以调节血栓形成风险,也可以潜在改善出血性疾病中的凝块不稳定性。本文综述了纤维蛋白原结合的抗纤维蛋白溶酶蛋白的主要特性、它们对血凝块溶解的影响以及与血栓形成或出血性疾病的关系。还讨论了这些蛋白质在针对纤维蛋白溶解系统的治疗策略中的作用,以治疗血栓形成性疾病或出血性疾病。