贾纳斯激酶
类风湿性关节炎
哮喘
Janus激酶3
托法替尼
免疫学
医学
药理学
细胞因子
化学
免疫系统
T细胞
抗原提呈细胞
作者
Mark Zak,Hart S. Dengler,Naomi S. Rajapaksa
标识
DOI:10.1016/j.bmcl.2019.126658
摘要
Multiple asthma-relevant cytokines including IL-4, IL-5, IL-13, and TSLP depend upon JAKs for signaling. JAK inhibition may, therefore, offer a novel intervention strategy for patients with disease refractory to current standards of care. Multiple systemically delivered JAK inhibitors have been approved for human use or are under clinical evaluation in autoimmune diseases such as rheumatoid arthritis. However, the on-target side effect profiles of these agents are likely not tolerable for many asthmatic patients. Limiting JAK inhibition to the lung is expected to improve therapeutic index relative to systemic inhibition. Thus, inhaled JAK inhibitors with lung-restricted exposure are of high interest as potential treatments for asthma.
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