Centre of Drug Discovery, State Key Laboratory of Bioactive Natural Products and Function, China.
Immunology. 2012 Feb;135(2):112-24. doi: 10.1111/j.1365-2567.2011.03522.x.
Interleukin-23 (IL-23) is a member of the IL-12 family of cytokines with pro-inflammatory properties. Its ability to potently enhance the expansion of T helper type 17 (Th17) cells indicates the responsibility for many of the inflammatory autoimmune responses. Emerging data demonstrate that IL-23 is a key participant in central regulation of the cellular mechanisms involved in inflammation. Both IL-23 and IL-17 form a new axis through Th17 cells, which has evolved in response to human diseases associated with immunoactivation and immunopathogeny, including bacterial or viral infections and chronic inflammation. Targeting of IL-23 or the IL-23 receptor or IL-23 axis is a potential therapeutic approach for autoimmune diseases including psoriasis, inflammatory bowel disease, rheumatoid arthritis and multiple sclerosis. The current review focuses on the immunobiology of IL-23 and summarizes the most recent findings on the role of IL-23 in the pre-clinical and ongoing clinical studies.
白细胞介素-23 (IL-23) 是白细胞介素 12 家族细胞因子的成员,具有促炎特性。它能够有力地增强辅助性 T 细胞 17(Th17)细胞的扩增,表明其对许多炎症性自身免疫反应负有责任。新出现的数据表明,IL-23 是参与炎症相关细胞机制的中央调控的关键参与者。IL-23 和 IL-17 通过 Th17 细胞形成一个新的轴,这是为了应对与免疫激活和免疫发病机制相关的人类疾病而进化的,包括细菌或病毒感染和慢性炎症。针对 IL-23 或 IL-23 受体或 IL-23 轴是治疗包括银屑病、炎症性肠病、类风湿关节炎和多发性硬化症在内的自身免疫性疾病的潜在方法。本综述重点介绍了 IL-23 的免疫生物学,并总结了最近关于 IL-23 在临床前和正在进行的临床研究中的作用的发现。