细胞因子释放综合征
生物
嵌合抗原受体
T细胞
耐火材料(行星科学)
免疫系统
细胞因子
免疫学
癌症研究
免疫疗法
细胞
受体
B细胞
不利影响
自身免疫性疾病
血小板
抗原
骨髓
T细胞受体
抗原处理
抗原提呈细胞
外围设备
Cd4 t细胞
细胞疗法
疾病
血小板活化
作者
Mengyan Wang,Tingting Liu,Qihua Dai,Jialin Teng,Yaping Wu,Jinchao Jia,Jianfen Meng,Yuning Ma,Hui Shi,Xiaobing Cheng,Honglei Liu,Yutong Su,Junna Ye,Huihui Chi,Zhuochao Zhou,Yue Sun,Yan Wu,Jia Chen,Wei Yin,Peng Gao
出处
期刊:Cell
[Cell Press]
日期:2026-09-01
标识
DOI:10.1016/j.cell.2026.08.039
摘要
While T cell engagers (TCEs) and chimeric antigen receptor (CAR)-T cell therapy show clinical promise for B cell depletion, challenges regarding safety, efficacy, and durability persist. ABO2203 is a lipid nanoparticle-formulated messenger RNA (mRNA) encoding a CD19-targeting TCE. In transgenic mice, ABO2203 induced complete B cell depletion with attenuated cytokine release compared with TCE protein. In a first-in-human study involving three patients with refractory secondary immune thrombocytopenia, ABO2203 achieved rapid and complete peripheral B cell depletion, with sustained depletion in bone marrow. Patients exhibited durable platelet recovery, improved serology, and reduced disease activity through 6 months of follow-up. ABO2203 was well tolerated, presenting only grade 1 and 2 adverse events without cytokine release syndrome. B cell reconstitution was observed with predominant transitional and naive B cells. These findings establish mRNA-encoded TCEs as a potent and safer therapeutic modality for B cell-mediated autoimmune diseases.
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