Center for Advanced Studies and Technology, Department of Medical, Oral and Biotechnology Science, "G. d'Annunzio" University of Chieti - Pescara, Chieti, Italy.
Center for Advanced Studies and Technology, Department of Medicine and Aging Sciences, "G. d'Annunzio" University of Chieti - Pescara, Chieti, Italy.
Front Immunol. 2020 Apr 28;11:581. doi: 10.3389/fimmu.2020.00581. eCollection 2020.
Non-resolving lung inflammation and infections are the underlying cause of morbidity and mortality in cystic fibrosis (CF). The endogenous lipid mediator resolvin (Rv) D1 is a potent regulator of resolution, and its roles, actions, and therapeutic potential in CF are of interest. Here, we investigated actions and efficacy of RvD1 in preclinical models of cystic fibrosis. knockout mice with chronic lung infection were treated with RvD1 to assess differences in lung bacterial load, inflammation, and tissue damage. Cells from volunteers with CF were treated with RvD1 during infection with , and effects on phagocytosis and inflammatory signaling were determined. In CF mice, RvD1 reduced bacterial burden, neutrophil infiltration, and histological signs of lung pathology, improving clinical scores of diseases. Mechanistically, RvD1 increased macrophage-mediated bacterial and leukocyte clearance . The clinical significance of these findings is supported by actions in primary leukocytes and epithelial cells from volunteers with CF where RvD1 enhanced phagocytosis and reduced genes and proteins associated to NF-κB activation and leukocyte infiltration. Concentration of RvD1 in sputum from patients with CF was also inversely correlated to those of cytokines and chemokines involved in CF lung pathology. These findings demonstrate efficacy of RvD1 in enhancing resolution of lung inflammation and infections and provide proof of concept for its potential as a prototypic novel pro-resolutive therapeutic approach for CF.
未解决的肺部炎症和感染是囊性纤维化(CF)发病和死亡的根本原因。内源性脂质介质消退素(Rv)D1 是解决问题的有效调节剂,其在 CF 中的作用、作用和治疗潜力引起了人们的兴趣。在这里,我们研究了 RvD1 在 CF 临床前模型中的作用和疗效。用 RvD1 治疗慢性肺部感染的 CF 基因敲除小鼠,以评估肺部细菌负荷、炎症和组织损伤的差异。用 RvD1 处理 CF 患者的细胞感染 ,并确定对吞噬作用和炎症信号的影响。在 CF 小鼠中,RvD1 降低了细菌负荷、中性粒细胞浸润和肺部病理的组织学迹象,改善了疾病的临床评分。在机制上,RvD1 增加了巨噬细胞介导的细菌和白细胞清除作用。CF 患者痰液中 RvD1 的浓度与 CF 肺部病理相关的细胞因子和趋化因子呈负相关,这一发现支持了这些发现的临床意义。这些发现表明 RvD1 在增强肺部炎症和感染的消退方面具有疗效,并为其作为 CF 新型促消退治疗方法的潜在应用提供了概念验证。