生物
多发性硬化
CD20
细胞因子释放综合征
中枢神经系统
嵌合抗原受体
抗原
脑脊液
单克隆抗体
细胞因子
细胞疗法
临床试验
细胞
炎症
单克隆
内科学
T细胞
单克隆抗体治疗
进行性疾病
受体
疾病
脱髓鞘病
免疫疗法
CD52型
免疫学
B细胞
遗传增强
临床孤立综合征
白细胞介素17
肿瘤坏死因子α
作者
Chuan Qin,Ming‐Hao Dong,Luo‐Qi Zhou,Yun‐Hui Chu,Xiao‐Wei Pang,Jiayi He,Ke Shang,Jun Xiao,Li Zhu,Huan Ye,Song-Bai Cai,Di Wang,Bi-Tao Bu,Gerd Meyer zu Hörste,Chunrui Li,Dai‐Shi Tian,Wei Wang
出处
期刊:Cell
[Cell Press]
日期:2025-10-15
卷期号:188 (23): 6414-6423.e11
被引量:10
标识
DOI:10.1016/j.cell.2025.09.020
摘要
Progressive multiple sclerosis (PMS), which is characterized by relentless disease progression, lacks effective treatment. While recent studies have highlighted the importance of B cells in driving compartmentalized central nervous system (CNS) inflammation in PMS pathogenesis, current B cell depletion therapies, such as CD20 monoclonal antibodies, face challenges in targeting plasma cells within the CNS. Here, we treated five patients with PMS (one primary PMS and four secondary PMS) with anti-B cell maturation antigen (BCMA) chimeric antigen receptor T (CAR-T) cell therapy in an ongoing phase 1 clinical trial (ClinicalTrials.gov: NCT04561557). Only grade 1 cytokine release syndrome was observed, and all grade ≥3 cytopenias occurred within 40 days post-infusion in all five patients. Meanwhile, we detected plasma cell depletion in CNS compartments, prolonged expansion and relieved exhaustion of CAR-T cells in the cerebrospinal fluid, and attenuation of microglial activation. These findings provided insights into the potential application of anti-BCMA CAR-T therapy for advancing clinical management of PMS.
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