Infectious Diseases Susceptibility Unit, Laboratory of Host Defenses, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 10 Center Drive, Building 10, CRC 6W-3750, Bethesda, MD 20892-1456, USA.
Curr Allergy Asthma Rep. 2011 Oct;11(5):369-77. doi: 10.1007/s11882-011-0212-9.
Primary immunodeficiencies are a heterogeneous group of genetically inherited diseases affecting the innate and adaptive immune systems that confer susceptibility to infection, autoimmunity, and cancer. Innate immunity includes neutrophils, macrophages, dendritic cells, natural killer cells, and natural killer T cells in conjunction with natural barriers (mostly skin and gastrointestinal and respiratory mucosa), as well as antimicrobial agents, opsonins (e.g., complement), and cytokines. Although somewhat primitive, innate immune cells can orchestrate discrete immune responses through the recognition of diverse pathogens by different pattern-recognition receptors. In this review, we discuss the most recent discoveries as well as the already established pathophysiologic mechanisms underlying innate immunity defects associated with primary immunodeficiencies.
原发性免疫缺陷是一组异质性的遗传性疾病,影响先天和适应性免疫系统,使机体易感染、发生自身免疫和癌症。先天免疫系统包括中性粒细胞、巨噬细胞、树突状细胞、自然杀伤细胞和自然杀伤 T 细胞,以及天然屏障(主要是皮肤、胃肠道和呼吸道黏膜),还有抗菌剂、调理素(如补体)和细胞因子。尽管先天免疫细胞有些原始,但它们可以通过不同的模式识别受体识别各种病原体,从而协调离散的免疫反应。在这篇综述中,我们讨论了与原发性免疫缺陷相关的先天免疫缺陷的最新发现以及已确立的病理生理机制。