Department of Microbiology and Immunology, State University of New York (SUNY) Upstate Medical University, Syracuse, NY, United States.
Front Cell Infect Microbiol. 2020 Nov 3;10:574417. doi: 10.3389/fcimb.2020.574417. eCollection 2020.
Dengue virus is an important human pathogen, infecting an estimated 400 million individuals per year and causing symptomatic disease in a subset of approximately 100 million. Much of the effort to date describing the host response to dengue has focused on the adaptive immune response, in part because of the well-established roles of antibody-dependent enhancement and T cell original sin as drivers of severe dengue upon heterotypic secondary infection. However, the innate immune system is a crucial factor in the host response to dengue, as it both governs the fate and vigor of the adaptive immune response, and mediates the acute inflammatory response in tissues. In this review, we discuss the innate inflammatory response to dengue infection, focusing on the role of evolutionarily conserved innate immune cells, their effector functions, and clinical course.
登革病毒是一种重要的人类病原体,估计每年感染 4 亿人,其中约有 1 亿人出现症状性疾病。迄今为止,描述宿主对登革热的反应的大部分工作都集中在适应性免疫反应上,部分原因是抗体依赖性增强和 T 细胞原始性作为异型二次感染导致重症登革热的驱动因素已得到充分证实。然而,先天免疫系统是宿主对登革热反应的关键因素,因为它既控制着适应性免疫反应的命运和活力,也调节组织中的急性炎症反应。在这篇综述中,我们讨论了登革热感染的先天炎症反应,重点讨论了进化上保守的先天免疫细胞及其效应功能和临床病程。