Recchiuti Antonio, Mattoscio Domenico, Isopi Elisa
Department of Medical, Oral and Biotechnological Science, Università "G. d'Annunzio" Chieti-Pescara, Chieti, Italy.
Centro di Scienze dell'Invecchiamento e Medicina Traslazionale (CeSI-MeT), Università "G. d'Annunzio" Chieti-Pescara, Chieti, Italy.
Front Pharmacol. 2019 Apr 2;10:252. doi: 10.3389/fphar.2019.00252. eCollection 2019.
Non-resolving inflammation is the main mechanism of morbidity and mortality among patients suffering from cystic fibrosis (CF), the most common life-threatening human genetic disease. Resolution of inflammation is an active process timely controlled by endogenous specialized pro-resolving lipid mediators (SPMs) produced locally in inflammatory loci to restrain this innate response, prevent further damages to the host, and permit return to homeostasis. Lipoxins, resolvins, protectins, and maresins are SPM derived from polyunsaturated fatty acids that limit excessive leukocyte infiltration and pro-inflammatory signals, stimulate innate microbial killing, and enhance resolution. Their unique chemical structures, receptors, and bioactions are being elucidated. Accruing data indicate that SPMs carry protective functions against unrelenting inflammation and infections in preclinical models and human CF systems. Here, we reviewed their roles and actions in controlling resolution of inflammation, evidence for their impairment in CF, and proofs of principle for their exploitation as innovative, non-immunosuppressive drugs to address inflammation and infections in CF.
炎症持续不消是囊性纤维化(CF)患者发病和死亡的主要机制,CF是人类最常见的危及生命的遗传性疾病。炎症消退是一个由内源性特异性促消退脂质介质(SPM)及时控制的主动过程,这些介质在炎症部位局部产生,以抑制这种固有反应,防止对宿主造成进一步损害,并使机体恢复到内环境稳态。脂氧素、消退素、保护素和maresin是源自多不饱和脂肪酸的SPM,它们可限制白细胞过度浸润和促炎信号,刺激先天性微生物杀伤,并促进炎症消退。它们独特的化学结构、受体和生物活性正在被阐明。越来越多的数据表明,在临床前模型和人类CF系统中,SPM对持续的炎症和感染具有保护作用。在此,我们综述了它们在控制炎症消退中的作用和作用机制,CF中它们功能受损的证据,以及将它们开发为创新的、非免疫抑制药物以解决CF中的炎症和感染的原理证明。