Department of Pathology and Laboratory Medicine, Centre for Blood Research, Life Science Institute, University of British Columbia, Vancouver, British Columbia, Canada.
Department of Biological Chemistry, University of Michigan Medical School, Ann Arbor, Michigan.
Semin Thromb Hemost. 2024 Oct;50(7):970-977. doi: 10.1055/s-0043-1768936. Epub 2023 May 16.
The contact pathway of blood clotting has received intense interest in recent years as studies have linked it to thrombosis, inflammation, and innate immunity. Because the contact pathway plays little to no role in normal hemostasis, it has emerged as a potential target for safer thromboprotection, relative to currently approved antithrombotic drugs which all target the final common pathway of blood clotting. Research since the mid-2000s has identified polyphosphate, DNA, and RNA as important triggers of the contact pathway with roles in thrombosis, although these molecules also modulate blood clotting and inflammation via mechanisms other than the contact pathway of the clotting cascade. The most significant source of extracellular DNA in many disease settings is in the form of neutrophil extracellular traps (NETs), which have been shown to contribute to incidence and severity of thrombosis. This review summarizes known roles of extracellular polyphosphate and nucleic acids in thrombosis, with an emphasis on novel agents under current development that target the prothrombotic activities of polyphosphate and NETs.
近年来,由于研究表明凝血接触途径与血栓形成、炎症和先天免疫有关,因此该途径受到了极大关注。由于凝血接触途径在正常止血中几乎不起作用,因此它已成为一种相对目前批准的抗血栓药物更安全的抗血栓保护的潜在靶点,这些药物都针对凝血级联的最终共同途径。自 21 世纪中期以来的研究已经确定多聚磷酸盐、DNA 和 RNA 是凝血接触途径的重要触发因素,在血栓形成中发挥作用,尽管这些分子也通过凝血级联的接触途径以外的机制调节凝血和炎症。在许多疾病情况下,细胞外 DNA 的最重要来源是以中性粒细胞胞外诱捕网(NETs)的形式存在,已经表明 NETs 有助于血栓形成的发生率和严重程度。本综述总结了细胞外多聚磷酸盐和核酸在血栓形成中的已知作用,重点介绍了目前正在开发的针对多聚磷酸盐和 NETs 促血栓形成活性的新型药物。