医学
泛发性脓疱性银屑病
银屑病
发病机制
单克隆抗体
受体
敌手
受体拮抗剂
单克隆
抗体
免疫学
皮肤病科
内科学
标识
DOI:10.1016/j.jaad.2024.01.034
摘要
The IL-36 signaling pathway dermatology revolution is underway. This pathway is key in the pathogenesis of generalized pustular psoriasis (GPP). The IL-36 receptor (IL-36R) antagonist spesolimab effectively manages GPP, rapidly controlling GPP flares and preventing their recurrence. A phase II trial of imsidolimab, a humanized IgG4 monoclonal antibody specifically binding IL-36R, demonstrated a rapid resolution of pustular eruptions in GPP patients.1
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