Genome Research Center for Allergy and Respiratory Disease, Division of Allergy and Respiratory Medicine, Soonchunhyang University Bucheon Hospital, Bucheon, Korea.
Allergy Asthma Immunol Res. 2010 Jul;2(3):188-94. doi: 10.4168/aair.2010.2.3.188. Epub 2010 May 17.
While much has indeed been learned about the biology and role of eosinophils, the paradigm of eosinophils has the pros and cons in development of asthma. To answer the questions in the black box, this review firstly discusses the biological and morphological differences between asthma and eosinophilic bronchitis (EB). EB is an interesting clinical manifestation of eosinophilic airway disease that does not involve airway hyperresponsiveness (AHR), demonstrating that airway eosinophilia alone is insufficient to merit a diagnosis of asthma. Secondly, I will describe and discuss the effect(s) of single-nucleotide polymorphisms (SNPs) in the genes CCR3, IL-5 RECEPTOR ALPHA (IL5RA), and IL1RL1, and finally the in vitro and in vivo effects of Notch inhibition on both eosinophil differentiation and experimental asthma. Eosinophilic airway inflammation is not as important in the pathogenesis and maintenance of asthma as had previously been thought. However, the role of eosinophils in other asthma subphenotypes, including refractory or severely remodeled asthma, needs to be evaluated further. High-throughput methodologies such as genomics will facilitate the discovery of new markers of inflammation; these, in turn, will aid in the evaluation of the role of eosinophils in asthma and its various subphenotypes.
虽然人们确实已经了解了嗜酸性粒细胞的生物学和作用,但嗜酸性粒细胞在哮喘发展中的范例既有优点也有缺点。为了回答黑盒中的问题,本综述首先讨论了哮喘和嗜酸性粒细胞性支气管炎(EB)之间的生物学和形态学差异。EB 是一种有趣的嗜酸性气道疾病的临床表现,不涉及气道高反应性(AHR),表明气道嗜酸性粒细胞增多本身不足以诊断为哮喘。其次,我将描述和讨论 CCR3、IL-5 受体 α(IL5RA)和 IL1RL1 基因中的单核苷酸多态性(SNPs)的作用,最后将描述和讨论 Notch 抑制对嗜酸性粒细胞分化和实验性哮喘的体外和体内作用。嗜酸性粒细胞性气道炎症在哮喘的发病机制和维持中的重要性不如以前认为的那么重要。然而,嗜酸性粒细胞在其他哮喘亚表型中的作用,包括难治性或严重重塑的哮喘,需要进一步评估。高通量方法,如基因组学,将有助于发现新的炎症标志物;这些反过来又将有助于评估嗜酸性粒细胞在哮喘及其各种亚表型中的作用。