Office of Science and Technology, National Institute of Arthritis Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Curr Opin Rheumatol. 2014 Mar;26(2):237-43. doi: 10.1097/BOR.0000000000000023.
Kinases inhibitors are now used for the treatment of autoimmune diseases. Here, the most recent findings related to their mechanism of action and some of the newest molecules and targets which are being investigated for autoimmune and inflammatory disorders are reviewed.
Similarly to p38 inhibitors, current spleen tyrosine kinase inhibitors have not fulfilled the expectations of researchers and clinicians, and will likely not be used therapeutically in autoimmunity. Bruton's tyrosine kinase inhibitors remain in the preclinical phase. Studies on the mechanism of action of successful Janus kinase (Jak) inhibitors have revealed that, apart from T and B cells, bone cells such as osteoclasts and innate immunity cells such as dendritic cells are positively affected. More specific, novel Jak inhibitors are now in clinical trials and newer Jak inhibitors are being developed. Other kinases are emerging from basic studies as potentially druggable and will surely be investigated.
First-generation pan-Jak inhibitors can be useful for a wide variety of diseases. They act on adaptive as well as innate immune cells and can promote tolerance. More specific inhibitors will soon be available and these may be used in a disease-specific manner.
激酶抑制剂现被用于治疗自身免疫性疾病。本文综述了作用机制的最新发现,以及正在研究用于自身免疫和炎症性疾病的最新分子和靶点。
与 p38 抑制剂类似,目前的脾酪氨酸激酶抑制剂并未达到研究人员和临床医生的预期,不太可能在自身免疫中进行治疗。布鲁顿酪氨酸激酶抑制剂仍处于临床前阶段。对成功的 Janus 激酶 (Jak) 抑制剂作用机制的研究表明,除了 T 和 B 细胞外,破骨细胞等骨细胞和树突状细胞等固有免疫细胞也受到了积极影响。更具特异性的新型 Jak 抑制剂现已进入临床试验,新型 Jak 抑制剂正在开发中。其他激酶也从基础研究中崭露头角,具有潜在的可成药性,肯定会得到进一步研究。
第一代泛 Jak 抑制剂可用于多种疾病。它们作用于适应性和固有免疫细胞,并可促进耐受。更具特异性的抑制剂即将面世,这些抑制剂可能会以特定疾病的方式使用。