Department of Respiratory Sciences, Institute for Lung Health, University of Leicester, Leicester, UK.
Department of Respiratory Diseases, Ghent University Hospital, Ghent, Belgium.
Allergy. 2020 Apr;75(4):761-768. doi: 10.1111/all.14001. Epub 2019 Aug 20.
Current research suggests that the prostaglandin D (PGD ) receptor 2 (DP ) is a principal regulator in the pathophysiology of asthma, because it stimulates and amplifies the inflammatory response in this condition. The DP receptor can be activated by both allergic and nonallergic stimuli, leading to several pro-inflammatory events, including eosinophil activation and migration, release of the type 2 cytokines interleukin (IL)-4, IL-5 and IL-13 from T helper 2 (Th2) cells and innate lymphoid cells type 2 (ILCs), and increased airway smooth muscle mass via recruitment of mesenchymal progenitors to the airway smooth muscle bundle. Activation of the DP receptor pathway has potential downstream effects on asthma pathophysiology, including on airway epithelial cells, mucus hypersecretion, and airway remodelling, and consequently might impact asthma symptoms and exacerbations. Given the broad distribution of DP receptors on immune and structural cells involved in asthma, this receptor is being explored as a novel therapeutic target.
目前的研究表明,前列腺素 D(PGD)受体 2(DP)是哮喘病理生理学的主要调节因子,因为它在这种情况下刺激和放大炎症反应。DP 受体可被过敏和非过敏刺激激活,导致几种促炎事件,包括嗜酸性粒细胞激活和迁移、2 型辅助性 T 细胞(Th2)和固有淋巴细胞 2 型(ILC2)释放 2 型细胞因子白细胞介素(IL)-4、IL-5 和 IL-13,以及通过募集间充质祖细胞到气道平滑肌束来增加气道平滑肌质量。DP 受体途径的激活对哮喘病理生理学具有潜在的下游影响,包括对气道上皮细胞、黏液高分泌和气道重塑的影响,因此可能会影响哮喘症状和加重。鉴于 DP 受体在参与哮喘的免疫和结构细胞中的广泛分布,该受体被作为一种新的治疗靶点进行探索。