达拉图穆马
医学
贝里穆马布
单克隆抗体
自身抗体
抗体依赖性细胞介导的细胞毒性
发病机制
等离子体电池
免疫抑制
抗体
单克隆
免疫学
B细胞激活因子
CD38
B细胞
川地34
生物
遗传学
干细胞
作者
Lennard Ostendorf,Marie E. Burns,Pawel Durek,Gitta Anne Heinz,Frederik Heinrich,Panagiotis Garantziotis,Philipp Enghard,Ulrich Richter,Robert Biesen,Udo Schneider,Fabian Knebel,Gerd R Burmester,Andreas Radbruch,Henrik E. Mei,Mir‐Farzin Mashreghi,Falk Hiepe,Tobias Alexander
标识
DOI:10.1056/nejmoa2023325
摘要
Daratumumab, a human monoclonal antibody that targets CD38, depletes plasma cells and is approved for the treatment of multiple myeloma. Long-lived plasma cells are implicated in the pathogenesis of systemic lupus erythematosus because they secrete autoantibodies, but they are unresponsive to standard immunosuppression. We describe the use of daratumumab that induced substantial clinical responses in two patients with life-threatening lupus, with the clinical responses sustained by maintenance therapy with belimumab, an antibody to B-cell activating factor. Significant depletion of long-lived plasma cells, reduction of interferon type I activity, and down-regulation of T-cell transcripts associated with chronic inflammation were documented. (Supported by the Deutsche Forschungsgemeinschaft and others.).
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