Department of Chest Disease, Strasbourg University Hospital, Strasbourg, France.
Equipe d'accueil 3072, University of Strasbourg, Strasbourg, France.
Front Immunol. 2019 Jul 23;10:1699. doi: 10.3389/fimmu.2019.01699. eCollection 2019.
Formerly considered as a passive process, the resolution of acute inflammation is now recognized as an active host response, with a cascade of coordinated cellular and molecular events that promotes termination of the inflammatory response and initiates tissue repair and healing. In a state of immune fitness, the resolution of inflammation is contained in time and space enabling the restoration of tissue homeostasis. There is increasing evidence that poor and/or inappropriate resolution of inflammation participates in the pathogenesis of chronic inflammatory diseases, extending in time the actions of pro-inflammatory mechanisms, and responsible in the long run for excessive tissue damage and pathology. In this review, we will focus on how resolution can be the target for therapy in "Th1/Th17 cell-driven" immune diseases and "Th2 cell-driven" immune diseases, with inflammatory bowel diseases (IBD) and asthma, as relevant examples. We describe the main cells and mediators stimulating the resolution of inflammation and discuss how pharmacological and dietary interventions but also life style factors, physical and psychological conditions, might influence the resolution phase. A better understanding of the impact of endogenous and exogenous factors on the resolution of inflammation might open a whole area in the development of personalized therapies in non-resolving chronic inflammatory diseases.
先前被认为是一个被动过程,急性炎症的消退现在被认为是宿主的主动反应,伴随着一系列协调的细胞和分子事件,促进炎症反应的终止,并启动组织修复和愈合。在免疫适应的状态下,炎症的消退是在时间和空间上受到控制的,从而使组织的内稳态得以恢复。越来越多的证据表明,炎症的消退不良和/或不适当参与了慢性炎症性疾病的发病机制,使促炎机制的作用时间延长,并最终导致过度的组织损伤和病理学。在这篇综述中,我们将重点讨论如何将消退作为“Th1/Th17 细胞驱动”免疫性疾病和“Th2 细胞驱动”免疫性疾病(如炎症性肠病(IBD)和哮喘)的治疗靶点。我们描述了刺激炎症消退的主要细胞和介质,并讨论了药理学和饮食干预以及生活方式因素、身体和心理状况如何影响消退阶段。更好地了解内源性和外源性因素对炎症消退的影响可能会为非消退性慢性炎症性疾病的个体化治疗开辟一个全新的领域。