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Biology and Pathogenesis of Thrombosis and Procoagulant Activity in Invasive Infections Caused by Group A Streptococci and Clostridium perfringens

机译:A组链球菌和产气荚膜梭菌引起的侵袭性感染的血栓形成和促凝血活性的生物学和发病机理

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摘要

Group A streptococcal necrotizing fasciitis/myonecrosis and Clostridium perfringens gas gangrene are two of the most fulminant gram-positive infections in humans. Tissue destruction associated with these infections progresses rapidly to involve an entire extremity. Multiple-organ failure is common, and morbidity and mortality remain high. Systemic activation of coagulation and dysregulation of the anticoagulation pathways contribute to the pathogenesis of many diverse disease entities of infectious etiology, and it has been our hypothesis that microvascular thrombosis contributes to reduced tissue perfusion, hypoxia, and subsequent regional tissue necrosis and organ failure in these invasive gram-positive infections. This article reviews the coagulation, anticoagulation, and fibrinolytic systems from cellular players to cytokines to novel antithrombotic therapies and discusses the mechanisms contributing to occlusive microvascular thrombosis and tissue destruction in invasive group A streptococcal and C. perfringens infections. A thorough understanding of these mechanisms may suggest novel therapeutic targets for patients with these devastating infections.
机译:A组链球菌坏死性筋膜炎/肌坏死和产气荚膜梭状芽胞杆菌坏疽是人类中最暴发的革兰氏阳性感染。与这些感染相关的组织破坏迅速发展,涉及整个肢体。多器官功能衰竭很常见,发病率和死亡率仍然很高。凝血的系统性激活和抗凝血途径的失调导致了多种传染病学病因的发病机理,并且我们的假设是微血管血栓形成有助于减少这些组织的灌注,缺氧以及随后的局部组织坏死和器官衰竭侵袭性革兰氏阳性感染。本文回顾了从细胞因子到细胞因子的凝血,抗凝和纤溶系统,再到新型抗血栓形成疗法,并讨论了侵入性A组链球菌和产气荚膜梭菌感染的闭塞性微血管血栓形成和组织破坏的机制。对这些机制的透彻了解可能为患有这些破坏性感染的患者提出了新的治疗靶标。

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