Miedema Jelle, Cinetto Francesco, Smed-Sörensen Anna, Spagnolo Paolo
Department of Pulmonary Medicine, Center of Expertise for Interstitial Lung Disease, Erasmus University Medical Center, Rotterdam, the Netherlands.
Rare Diseases Referral Center, Internal Medicine 1, Ca' Foncello Hospital, AULSS2 Marca Trevigiana, Italy; Department of Medicine - DIMED, University of Padova, Padova, Italy.
J Autoimmun. 2024 Dec;149:103247. doi: 10.1016/j.jaut.2024.103247. Epub 2024 May 10.
Sarcoidosis is a granulomatous multiorgan disease, thought to result from exposure to yet unidentified antigens in genetically susceptible individuals. The exaggerated inflammatory response that leads to granuloma formation is highly complex and involves the innate and adaptive immune system. Consecutive immunological studies using advanced technology have increased our understanding of aberrantly activated immune cells, mediators and pathways that influence the formation, maintenance and resolution of granulomas. Over the years, it has become increasingly clear that disease immunopathogenesis can only be understood if the clinical heterogeneity of sarcoidosis is taken into consideration, along with the distribution of immune cells in peripheral blood and involved organs. Most studies offer an immunological snapshot during disease course, while the cellular composition of both the circulation and tissue microenvironment may change over time. Despite these challenges, novel insights on the role of the immune system are continuously published, thus bringing the field forward. This review highlights current knowledge on the innate and adaptive immune responses involved in sarcoidosis pathogenesis, as well as the pathways involved in non-resolving disease and fibrosis development. Additionally, we describe proposed immunological mechanisms responsible for drug-induced sarcoid like reactions. Although many aspects of disease immunopathogenesis remain to be unraveled, the identification of crucial immune reactions in sarcoidosis may help identify new treatment targets. We therefore also discuss potential therapies and future strategies based on the latest immunological findings.
结节病是一种肉芽肿性多器官疾病,被认为是由于基因易感个体接触了尚未明确的抗原所致。导致肉芽肿形成的过度炎症反应非常复杂,涉及固有免疫系统和适应性免疫系统。使用先进技术进行的一系列免疫学研究增进了我们对异常激活的免疫细胞、介质和影响肉芽肿形成、维持及消散的信号通路的理解。多年来,越来越清楚的是,只有考虑到结节病的临床异质性以及外周血和受累器官中免疫细胞的分布,才能理解疾病的免疫发病机制。大多数研究提供的是疾病过程中的免疫学快照,而循环系统和组织微环境中的细胞组成可能随时间而变化。尽管存在这些挑战,但关于免疫系统作用的新见解仍在不断发表,从而推动了该领域的发展。本综述重点介绍了目前关于结节病发病机制中固有免疫和适应性免疫反应的知识,以及与疾病不缓解和纤维化发展相关的信号通路。此外,我们还描述了药物诱导的类结节病反应的免疫机制。尽管疾病免疫发病机制的许多方面仍有待阐明,但确定结节病中的关键免疫反应可能有助于确定新的治疗靶点。因此,我们还将根据最新的免疫学发现讨论潜在的治疗方法和未来策略。