医学
贝里穆马布
临床试验
免疫学
系统性红斑狼疮
药品
促炎细胞因子
红斑狼疮
细胞因子
药理学
疾病
内科学
抗体
炎症
B细胞
B细胞激活因子
作者
Ankeet S. Bhatt,Pooja Gupta,Richard Furie,Himanshu Vashistha
标识
DOI:10.1080/13543784.2025.2473060
摘要
High levels of IFN-I (type 1 interferon) are present in most SLE patients, making this pathway an attractive target for drug development. Litifilimab downregulates IFN-I by targeting BDCA2, while dexadilimab targets ILT7 to recruit effector cells, reducing IFN-I production by killing PDCs. Anifrolumab binds to the IFN-I receptor, blocking the activity of all IFN-Is, and deucravacitinib reduces IFN-I by inhibiting TYK2, thereby interfering with downstream signaling. Therapies that target IFN-I represents a promising class of medications for SLE patients.
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