Mertz Philippe, Hentgen Véronique, Boursier Guilaine, Elhani Ines, Calas Laure, Delon Jerome, Georgin-Lavialle Sophie
Sorbonne université, hôpital Tenon, DMU3ID, APHP, ERN RITA, Paris, France; Centre de référence des maladies auto-inflammatoires et de l'amylose inflammatoire (CEREMAIA), Paris, France; Centre hospitalier de Versailles, 78150 le Chesnay, France; Institut Cochin, Inserm, CNRS, université Paris Cité, F-75014 Paris, France.
Centre de référence des maladies auto-inflammatoires et de l'amylose inflammatoire (CEREMAIA), Paris, France; Centre hospitalier de Versailles, 78150 le Chesnay, France.
Rev Med Interne. 2025 Mar;46(3):155-163. doi: 10.1016/j.revmed.2024.08.003. Epub 2024 Aug 17.
Autoinflammatory diseases (AIDs) are conditions characterized by dysfunction of innate immunity, causing systemic inflammation and various clinical symptoms. The field of AIDs has expanded due to improved comprehension of pathophysiological mechanisms and advancements in genomics techniques. A new emerging category of AIDs is characterized by a significant increase in interleukin 18 (IL-18), a pro-inflammatory cytokine synthesized in macrophages and activated by caspase 1 via various inflammasomes. IL-18 plays a role in the regulation of innate and adaptive immunity. IL-18 is involved in various functions, such as the proliferation, survival, and differentiation of immune cells, tissue infiltration of immune cells, polarization of immune responses, and production of other pro-inflammatory cytokines. This review analyzes the literature on IL-18 regarding its functions and its implications in the diagnosis and treatment of AIDs. IL-18-associated AIDs comprise Still's disease and diseases associated with mutations in NLRC4, XIAP, CDC42, and PSTPIP1, as well as IL-18BP deficiencies. With the exception of PSTPIP1-associated diseases, these conditions all carry a risk of macrophagic activation syndrome. Measuring IL-18 levels in serum can aid in the diagnosis, prognosis, and monitoring of these diseases. Therapies targeting IL-18 and its signaling pathways are currently under investigation.
自身炎症性疾病(AIDs)是一类以固有免疫功能障碍为特征的疾病,可导致全身炎症和各种临床症状。由于对病理生理机制的理解有所提高以及基因组学技术的进步,自身炎症性疾病领域不断扩展。一类新出现的自身炎症性疾病的特征是白细胞介素18(IL-18)显著增加,IL-18是一种在巨噬细胞中合成并通过各种炎性小体被半胱天冬酶1激活的促炎细胞因子。IL-18在固有免疫和适应性免疫的调节中发挥作用。IL-18参与多种功能,如免疫细胞的增殖、存活和分化、免疫细胞的组织浸润、免疫反应的极化以及其他促炎细胞因子的产生。本综述分析了关于IL-18的功能及其在自身炎症性疾病诊断和治疗中的意义的文献。与IL-18相关的自身炎症性疾病包括斯蒂尔病以及与NLRC4、XIAP、CDC42和PSTPIP1突变相关的疾病,还有IL-18BP缺陷。除了与PSTPIP1相关的疾病外,这些病症都有巨噬细胞活化综合征的风险。检测血清中的IL-18水平有助于这些疾病的诊断、预后评估和监测。目前正在研究针对IL-18及其信号通路的疗法。