UBC James Hogg Research Centre Heart + Lung Institute, St Pauls Hospital, Vancouver, BC, V6Z 1Y6, Canada.
Curr Opin Immunol. 2012 Dec;24(6):740-6. doi: 10.1016/j.coi.2012.08.012. Epub 2012 Oct 19.
The innate immunity function of the human airway epithelium is responsible for orchestrating defence against inhaled viruses, bacteria, fungi, allergens, pollution, and other environmental insults. Epithelial cells present a mechanically tight, pseudostratified, multi-cell barrier that secretes mucus, surfactants, and anti-microbial peptides to manage minor insults. Secondary to the mechanical impedances, cell surface and cytoplasmic pattern recognition receptors await detection of more aggressive insults. The differentiation state of the airway epithelium contributes to innate immunity by compartmentalizing receptors and mediator production. Activation of innate immune receptors triggers production of interferons, cytokines, and chemokines, which influence adaptive immune responses. Mounting evidence suggests that these responses are aberrant in asthma and may contribute to disease progression and exacerbations. In this review, we discuss the recent evidence supporting these statements, focusing primarily on data generated from using human samples.
人体气道上皮的先天免疫功能负责协调防御吸入的病毒、细菌、真菌、过敏原、污染和其他环境损伤。上皮细胞呈现出机械紧密的假复层多细胞屏障,分泌黏液、表面活性剂和抗菌肽来应对较小的损伤。由于机械阻抗的存在,细胞表面和细胞质模式识别受体等待检测更具侵袭性的损伤。气道上皮的分化状态通过分隔受体和介质产生来促进先天免疫。先天免疫受体的激活触发干扰素、细胞因子和趋化因子的产生,从而影响适应性免疫反应。越来越多的证据表明,这些反应在哮喘中是异常的,可能导致疾病进展和加重。在这篇综述中,我们讨论了支持这些观点的最新证据,主要集中在使用人类样本获得的数据上。