Divisions of Cardiology and Rheumatology, Department of Medicine, University of Florida, Gainesville, Florida, USA.
Antimicrob Agents Chemother. 2013 Sep;57(9):4114-27. doi: 10.1128/AAC.02594-12. Epub 2013 Jun 17.
Lethal viral infections produce widespread inflammation with vascular leak, clotting, and bleeding (disseminated intravascular coagulation [DIC]), organ failure, and high mortality. Serine proteases in clot-forming (thrombotic) and clot-dissolving (thrombolytic) cascades are activated by an inflammatory cytokine storm and also can induce systemic inflammation with loss of normal serine protease inhibitor (serpin) regulation. Myxomavirus secretes a potent anti-inflammatory serpin, Serp-1, that inhibits clotting factor X (fX) and thrombolytic tissue- and urokinase-type plasminogen activators (tPA and uPA) with anti-inflammatory activity in multiple animal models. Purified serpin significantly improved survival in a murine gammaherpesvirus 68 (MHV68) infection in gamma interferon receptor (IFN-γR) knockout mice, a model for lethal inflammatory vasculitis. Treatment of MHV68-infected mice with neuroserpin, a mammalian serpin that inhibits only tPA and uPA, was ineffective. Serp-1 reduced virus load, lung hemorrhage, and aortic, lung, and colon inflammation in MHV68-infected mice and also reduced virus load. Neuroserpin suppressed a wide range of immune spleen cell responses after MHV68 infection, while Serp-1 selectively increased CD11c(+) splenocytes (macrophage and dendritic cells) and reduced CD11b(+) tissue macrophages. Serp-1 altered gene expression for coagulation and inflammatory responses, whereas neuroserpin did not. Serp-1 treatment was assessed in a second viral infection, mouse-adapted Zaire ebolavirus in wild-type BALB/c mice, with improved survival and reduced tissue necrosis. In summary, treatment with this unique myxomavirus-derived serpin suppresses systemic serine protease and innate immune responses caused by unrelated lethal viral infections (both RNA and DNA viruses), providing a potential new therapeutic approach for treatment of lethal viral sepsis.
致命性病毒感染会引发广泛的炎症反应,包括血管渗漏、凝血、出血(弥散性血管内凝血 [DIC])、器官衰竭和高死亡率。血栓形成(血栓形成)和血栓溶解(溶栓)级联中的丝氨酸蛋白酶被炎症细胞因子风暴激活,也可以诱导全身炎症,导致正常丝氨酸蛋白酶抑制剂(丝氨酸蛋白酶抑制剂)失去调节。粘液瘤病毒分泌一种强效的抗炎丝氨酸蛋白酶抑制剂 Serp-1,它可以抑制凝血因子 X (fX) 和溶栓组织型和尿激酶型纤溶酶原激活剂 (tPA 和 uPA),并在多种动物模型中具有抗炎活性。纯化的丝氨酸蛋白酶抑制剂在γ干扰素受体 (IFN-γR) 敲除小鼠的γ疱疹病毒 68 (MHV68) 感染模型中显著提高了生存率,该模型是致命性炎症性血管炎。用神经丝氨酸蛋白酶抑制剂(一种仅抑制 tPA 和 uPA 的哺乳动物丝氨酸蛋白酶抑制剂)治疗 MHV68 感染的小鼠无效。Serp-1 降低了 MHV68 感染小鼠的病毒载量、肺出血以及主动脉、肺和结肠的炎症,并降低了病毒载量。神经丝氨酸蛋白酶抑制剂抑制了 MHV68 感染后广泛的免疫脾细胞反应,而 Serp-1 则选择性地增加了 CD11c(+) 脾细胞(巨噬细胞和树突状细胞)并减少了 CD11b(+) 组织巨噬细胞。Serp-1 改变了凝血和炎症反应的基因表达,而神经丝氨酸蛋白酶抑制剂则没有。Serp-1 治疗在第二种病毒感染,即野生型 BALB/c 小鼠中的适应小鼠的扎伊尔埃博拉病毒中进行了评估,结果显示生存率提高,组织坏死减少。总之,用这种独特的粘液瘤病毒衍生的丝氨酸蛋白酶抑制剂治疗与无关的致命性病毒感染(包括 RNA 和 DNA 病毒)引起的全身性丝氨酸蛋白酶和固有免疫反应,可以为治疗致命性病毒败血症提供一种新的潜在治疗方法。