Institute for Research in Molecular Medicine (INFORMM), Universiti Sains Malaysia, 11800, Minden, Penang, Malaysia.
Inflamm Res. 2020 May;69(5):463-480. doi: 10.1007/s00011-020-01339-9. Epub 2020 Mar 25.
IL-23 is a central proinflammatory cytokine with a wide range of influence over immune response. It is implicated in several autoimmune diseases due to the infinite inflammatory loops it can create through the positive feedbacks of both IL-17 and IL-22 arms. This made IL-23 a key target of autoimmune disorders therapy, which indeed was proven to inhibit inflammation and ameliorate diseases. Current autoimmune treatments targeting IL-23 are either by preventing IL-23 ligation to its receptor (IL-23R) via antibodies or inhibiting IL-23 signaling by signaling downstream mediators' inhibitors, with each approach having its own pros and cons.
Literature review was done to further understand the biology of IL-23 and current therapies.
In this review, we discuss the biological features of IL-23 and its role in the pathogenesis of autoimmune diseases including psoriasis, rheumatoid arthritis and inflammatory bowel diseases. Advantages, limitations and side effects of each concept will be reviewed, suggesting several advanced IL-23-based bio-techniques to generate new and possible future therapies to overcome current treatments problems.
IL-23 是一种重要的促炎细胞因子,对免疫反应有广泛的影响。由于它可以通过 IL-17 和 IL-22 臂的正反馈产生无限的炎症循环,因此它与多种自身免疫性疾病有关。这使得 IL-23 成为自身免疫性疾病治疗的一个关键靶点,事实证明它可以抑制炎症并改善疾病。目前针对 IL-23 的自身免疫治疗方法要么是通过抗体阻止 IL-23 与其受体(IL-23R)结合,要么是通过抑制信号下游介质的抑制剂来抑制 IL-23 信号,每种方法都有其自身的优缺点。
通过文献回顾进一步了解 IL-23 的生物学特性及其在包括银屑病、类风湿关节炎和炎症性肠病在内的自身免疫性疾病发病机制中的作用。将讨论每种方法的优点、局限性和副作用,提出几种基于 IL-23 的先进生物技术,以产生新的和可能的未来疗法,克服当前治疗方法的问题。