Thrombosis and Hemostasis Program, Division of Hematology and Oncology, Department of Medicine, University of North Carolina McAllister Heart Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Blood. 2014 Apr 24;123(17):2605-13. doi: 10.1182/blood-2013-09-526277. Epub 2014 Mar 14.
The coagulation cascade is activated during viral infections. This response may be part of the host defense system to limit spread of the pathogen. However, excessive activation of the coagulation cascade can be deleterious. In fact, inhibition of the tissue factor/factor VIIa complex reduced mortality in a monkey model of Ebola hemorrhagic fever. Other studies showed that incorporation of tissue factor into the envelope of herpes simplex virus increases infection of endothelial cells and mice. Furthermore, binding of factor X to adenovirus serotype 5 enhances infection of hepatocytes but also increases the activation of the innate immune response to the virus. Coagulation proteases activate protease-activated receptors (PARs). Interestingly, we and others found that PAR1 and PAR2 modulate the immune response to viral infection. For instance, PAR1 positively regulates TLR3-dependent expression of the antiviral protein interferon β, whereas PAR2 negatively regulates expression during coxsackievirus group B infection. These studies indicate that the coagulation cascade plays multiple roles during viral infections.
在病毒感染期间,凝血级联被激活。这种反应可能是宿主防御系统的一部分,以限制病原体的传播。然而,凝血级联的过度激活可能是有害的。事实上,在埃博拉出血热的猴子模型中,组织因子/因子 VIIa 复合物的抑制降低了死亡率。其他研究表明,将组织因子纳入单纯疱疹病毒包膜中会增加内皮细胞和小鼠的感染。此外,因子 X 与腺病毒血清型 5 的结合增强了肝细胞的感染,但也增加了对病毒的固有免疫反应的激活。凝血蛋白酶激活蛋白酶激活受体(PARs)。有趣的是,我们和其他人发现 PAR1 和 PAR2 调节病毒感染的免疫反应。例如,PAR1 正向调节 TLR3 依赖性抗病毒蛋白干扰素 β 的表达,而 PAR2 在柯萨奇病毒 B 感染期间负调节表达。这些研究表明,凝血级联在病毒感染过程中发挥多种作用。