医学
单克隆抗体
免疫学
红斑狼疮
皮肤病科
抗体
作者
Richard Furie,Victoria P. Werth,Joseph F. Merola,Lauren Stevenson,Taylor L. Reynolds,Himanshu Naik,Wenting Wang,Romy Christmann,Agnès Gardet,Alex Pellerin,Stefan Hamann,Pavan K. Auluck,Catherine Barbey,Parul Gulati,Dania Rabah,Nathalie Franchimont
摘要
BACKGROUND. Plasmacytoid DCs (pDC) produce large amounts of type I IFN (IFN-I), cytokines convincingly linked to systemic lupus erythematosus (SLE) pathogenesis. BIIB059 is a humanized mAb that binds blood DC antigen 2 (BDCA2), a pDC-specific receptor that inhibits the production of IFN-I and other inflammatory mediators when ligated. A first-in-human study was conducted to assess safety, tolerability, and pharmacokinetic (PK) and pharmacodynamic (PD) effects of single BIIB059 doses in healthy volunteers (HV) and patients with SLE with active cutaneous disease as well as proof of biological activity and preliminary clinical response in the SLE cohort.
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