Department of Critical Care Medicine, Snyder Institute for Chronic Diseases, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Department of Pediatrics, Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Front Immunol. 2019 Oct 11;10:2400. doi: 10.3389/fimmu.2019.02400. eCollection 2019.
Despite their humble origins as anuclear fragments of megakaryocytes, platelets have emerged as versatile mediators of thrombosis and immunity. The diverse spectrum of platelet functions are on full display during the host response to severe infection and sepsis, with platelets taking center-stage in the intravascular immune response to blood-borne pathogens. Platelets are endowed with a comprehensive armamentarium of pathogen detection systems that enable them to function as sentinels in the bloodstream for rapid identification of microbial invasion. Through both autonomous anti-microbial effector functions and collaborations with other innate immune cells, platelets orchestrate a complex intravascular immune defense system that protects against bacterial dissemination. As with any powerful immune defense system, dysregulation of platelet-mediated intravascular immunity can lead to profound collateral damage to host cells and tissues, resulting in sepsis-associated organ dysfunction. In this article, the cellular and molecular contributions of platelets to intravascular immune defenses in sepsis will be reviewed, including the roles of platelets in surveillance of the microcirculation and elicitation of protective anti-bacterial responses. Mechanisms of platelet-mediated thromboinflammatory organ dysfunction will be explored, with linkages to clinical biomarkers of platelet homeostasis that aid in the diagnosis and prognostication of human sepsis. Lastly, we discuss novel therapeutic opportunities that take advantage of our evolving understanding of platelets and intravascular immunity in severe infection.
尽管血小板起源卑微,只是巨核细胞的核碎片,但它们已成为血栓形成和免疫的多功能介质。在宿主对严重感染和败血症的反应中,血小板的各种功能表现得淋漓尽致,在血液传播病原体的血管内免疫反应中,血小板成为主角。血小板拥有一套全面的病原体检测系统,使它们能够在血液中充当快速识别微生物入侵的哨兵。通过自主的抗菌效应功能以及与其他先天免疫细胞的合作,血小板协调了一个复杂的血管内免疫防御系统,以防止细菌传播。与任何强大的免疫防御系统一样,血小板介导的血管内免疫失调可能导致宿主细胞和组织的严重损伤,从而导致与败血症相关的器官功能障碍。在本文中,将回顾血小板在败血症中对血管内免疫防御的细胞和分子贡献,包括血小板在监测微循环和引发保护性抗细菌反应中的作用。还将探讨血小板介导的血栓炎症性器官功能障碍的机制,并与血小板稳态的临床生物标志物联系起来,以辅助人类败血症的诊断和预后。最后,我们讨论了利用我们对严重感染中血小板和血管内免疫的不断深入理解而产生的新的治疗机会。