嗜酸性粒细胞与慢性阻塞性肺病的相关性:炎症、微生物组和临床结果。

IF 3.6 3区 医学 Q3 CELL BIOLOGY
Andrew Higham, Augusta Beech, Dave Singh
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引用次数: 0

摘要

慢性阻塞性肺病(COPD)是由吸入香烟烟雾等有害微粒引起的。其病理生理学特征包括气道炎症、肺泡破坏和可逆性差的气流阻塞。慢性阻塞性肺病患者中有一个亚群的血液嗜酸性粒细胞计数(BEC)较高,这与吸入皮质类固醇的反应增加和肺部 2 型(T2)炎症的生物标志物增加有关。新的证据显示,肺嗜酸性粒细胞计数增加的慢性阻塞性肺病患者的气道微生物组发生了改变。较高的 BECs 也与肺功能衰退加剧有关,这表明 T2 型炎症与慢性阻塞性肺病的渐进病理生理学有关。我们对嗜酸性粒细胞和 T2 炎症在慢性阻塞性肺病病理生理学中的作用进行了叙述性综述,包括肺微生物组、针对慢性阻塞性肺病 T2 通路的药物治疗以及将 BEC 作为慢性阻塞性肺病生物标志物的临床应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The relevance of eosinophils in chronic obstructive pulmonary disease: inflammation, microbiome, and clinical outcomes.

Chronic obstructive pulmonary disease is caused by the inhalation of noxious particles such as cigarette smoke. The pathophysiological features include airway inflammation, alveolar destruction, and poorly reversible airflow obstruction. A subgroup of patients with chronic obstructive pulmonary disease has higher blood eosinophil counts, associated with an increased response to inhaled corticosteroids and increased biomarkers of pulmonary type 2 inflammation. Emerging evidence shows that patients with chronic obstructive pulmonary disease with increased pulmonary eosinophil counts have an altered airway microbiome. Higher blood eosinophil counts are also associated with increased lung function decline, implicating type 2 inflammation in progressive pathophysiology in chronic obstructive pulmonary disease. We provide a narrative review of the role of eosinophils and type 2 inflammation in the pathophysiology of chronic obstructive pulmonary disease, encompassing the lung microbiome, pharmacological targeting of type 2 pathways in chronic obstructive pulmonary disease, and the clinical use of blood eosinophil count as a chronic obstructive pulmonary disease biomarker.

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来源期刊
Journal of Leukocyte Biology
Journal of Leukocyte Biology 医学-免疫学
CiteScore
11.50
自引率
0.00%
发文量
358
审稿时长
2 months
期刊介绍: JLB is a peer-reviewed, academic journal published by the Society for Leukocyte Biology for its members and the community of immunobiologists. The journal publishes papers devoted to the exploration of the cellular and molecular biology of granulocytes, mononuclear phagocytes, lymphocytes, NK cells, and other cells involved in host physiology and defense/resistance against disease. Since all cells in the body can directly or indirectly contribute to the maintenance of the integrity of the organism and restoration of homeostasis through repair, JLB also considers articles involving epithelial, endothelial, fibroblastic, neural, and other somatic cell types participating in host defense. Studies covering pathophysiology, cell development, differentiation and trafficking; fundamental, translational and clinical immunology, inflammation, extracellular mediators and effector molecules; receptors, signal transduction and genes are considered relevant. Research articles and reviews that provide a novel understanding in any of these fields are given priority as well as technical advances related to leukocyte research methods.
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