医学
贝里穆马布
美罗华
羟基氯喹
系统性红斑狼疮
塞库金单抗
免疫学
疾病
红斑狼疮
皮肤病科
乌斯特基努马
重症监护医学
英夫利昔单抗
银屑病性关节炎
银屑病
内科学
淋巴瘤
传染病(医学专业)
B细胞
2019年冠状病毒病(COVID-19)
B细胞激活因子
抗体
作者
Hong Shi,Jóhann E. Guðjónsson,J. Michelle Kahlenberg
标识
DOI:10.1097/bor.0000000000000704
摘要
Purpose of review Cutaneous lupus erythematosus (CLE) is a highly heterogeneous autoimmune disease. No specific Federal Drug Administration-approved therapies for CLE-alone are available, and resistance to conventional treatments is common. This review will summarize current treatment approaches and pending treatment strategies. Recent findings Research into the pathogenesis of CLE is accelerating. A skewed type I interferon production and response contribute to CLE lesions. The pathophysiology of lesions may be similar among the lesional subtypes, and patients with a more TLR9-driven disease mechanism may have more benefit from hydroxychloroquine. Case reports continue to support the use of dapsone for CLE, especially bullous lupus erythematosus. Rituximab and Belimumab have efficacy in patients with systemic lupus erythematosus and severe active CLE. The significant role for type I interferons in CLE and encouraging clinical data suggest anifrolumab as a very promising agent for CLE. Dapirolizumab, BIIB059, Ustekinumab and Janus kinase inhibitors also have supportive early data as promising new strategies for CLE treatment. Summary Continued research to understand the mechanisms driving CLE will facilitate the development and approval of new targets. The pipeline for new treatments is rich.
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