免疫性血小板减少症
单克隆抗体
CD38
免疫学
抗体
医学
免疫系统
病毒学
生物
川地34
干细胞
遗传学
作者
Yunfei Chen,Yanmei Xu,Huiyuan Li,Ting Sun,Xuan Cao,Yuhua Wang,Feng Xue,Wei Liu,Xiaofan Liu,H. Dong,Rongfeng Fu,Xinyue Dai,Wentian Wang,Yueshen Ma,Zhen Song,Ying Chi,Mankai Ju,Wenjing Gu,Xiaolei Pei,Renchi Yang
标识
DOI:10.1056/nejmoa2400409
摘要
BACKGROUND: Immune thrombocytopenia (ITP) is an autoimmune disease characterized by autoantibody-mediated platelet destruction. Treatment with CM313, a novel anti-CD38 monoclonal antibody, can result in targeted clearance of CD38-positive cells, including plasma cells. METHODS: per liter within 8 weeks after the first dose of CM313. The status of peripheral-blood immune cells in patients and changes in the mononuclear phagocytic system in passive mouse models of ITP receiving anti-CD38 therapy were monitored. RESULTS: CD16+ natural killer cells, the expression of CD32b on monocytes in peripheral blood, and the number of macrophages in the spleen of the passive mouse models of ITP all decreased. CONCLUSIONS: In this study, anti-CD38 targeted therapy rapidly boosted platelet levels by inhibiting antibody-dependent cell-mediated cytotoxicity on platelets, maintained long-term efficacy by clearing plasma cells, and was associated with mainly low-grade toxic effects. (Funded by the Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences and others; ClinicalTrials.gov number, NCT05694767).
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