Cardiovascular and Metabolic Disorders Program, Duke-National University of Singapore Medical School, 169857 Singapore, Singapore; email:
National Heart Research Institute Singapore, National Heart Centre Singapore, 169609 Singapore, Singapore.
Annu Rev Med. 2020 Jan 27;71:263-276. doi: 10.1146/annurev-med-041818-011649.
Interleukin (IL)-11 is upregulated in a wide variety of fibro-inflammatory diseases such as systemic sclerosis, rheumatoid arthritis, pulmonary fibrosis, inflammatory bowel disease, kidney disease, drug-induced liver injury, and nonalcoholic steatohepatitis. IL-11 is a member of the IL-6 cytokine family and has several distinct properties that define its unique and nonredundant roles in disease. The IL-11 receptor is highly expressed on stromal, epithelial and polarized cells, where noncanonical IL-11 signaling drives the three pathologies common to all fibro-inflammatory diseases-myofibroblast activation, parenchymal cell dysfunction, and inflammation-while also inhibiting tissue regeneration. This cytokine has been little studied, and publications on IL-11 peaked in the early 1990s, when it was largely misunderstood. Here we describe recent advances in our understanding of IL-11 biology, outline how misconceptions as to its function came about, and highlight the large potential of therapies targeting IL-11 signaling for treating human disease.
白细胞介素 (IL)-11 在多种纤维炎症性疾病中上调,如系统性硬化症、类风湿关节炎、肺纤维化、炎症性肠病、肾病、药物性肝损伤和非酒精性脂肪性肝炎。IL-11 是白细胞介素 6 细胞因子家族的一员,具有多种独特的特性,定义了其在疾病中的独特且不可或缺的作用。IL-11 受体在基质细胞、上皮细胞和极化细胞上高度表达,其中非典型的 IL-11 信号通路驱动所有纤维炎症性疾病共有的三种病理改变——肌成纤维细胞激活、实质细胞功能障碍和炎症——同时抑制组织再生。这种细胞因子研究甚少,关于 IL-11 的出版物在 20 世纪 90 年代达到顶峰,当时人们对其功能存在很大的误解。在这里,我们描述了我们对 IL-11 生物学的最新理解,概述了其功能的误解是如何产生的,并强调了靶向 IL-11 信号通路治疗人类疾病的巨大潜力。