Human Lung Mast Cells: Therapeutic Implications in Asthma

免疫学 免疫系统 哮喘 肥大细胞 白细胞介素33 医学 免疫球蛋白E 炎症 单克隆抗体 先天免疫系统 获得性免疫系统 生物 抗体 白细胞介素 细胞因子 内科学
作者
Remo Poto,Gjada Criscuolo,Gianni Marone,Christopher Brightling,Gilda Varricchi
出处
期刊:International Journal of Molecular Sciences [MDPI AG]
卷期号:23 (22): 14466-14466 被引量:11
标识
DOI:10.3390/ijms232214466
摘要

Mast cells are strategically located in different compartments of the lung in asthmatic patients. These cells are widely recognized as central effectors and immunomodulators in different asthma phenotypes. Mast cell mediators activate a wide spectrum of cells of the innate and adaptive immune system during airway inflammation. Moreover, these cells modulate the activities of several structural cells (i.e., fibroblasts, airway smooth muscle cells, bronchial epithelial and goblet cells, and endothelial cells) in the human lung. These findings indicate that lung mast cells and their mediators significantly contribute to the immune induction of airway remodeling in severe asthma. Therapies targeting mast cell mediators and/or their receptors, including monoclonal antibodies targeting IgE, IL-4/IL-13, IL-5/IL-5Rα, IL-4Rα, TSLP, and IL-33, have been found safe and effective in the treatment of different phenotypes of asthma. Moreover, agonists of inhibitory receptors expressed by human mast cells (Siglec-8, Siglec-6) are under investigation for asthma treatment. Increasing evidence suggests that different approaches to depleting mast cells show promising results in severe asthma treatment. Novel treatments targeting mast cells can presumably change the course of the disease and induce drug-free remission in bronchial asthma. Here, we provide an overview of current and promising treatments for asthma that directly or indirectly target lung mast cells.
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