Anti-BCMA CAR-T therapy in patients with progressive multiple sclerosis

Chuan Qin(Huazhong University of Science and Technology), Ming‐Hao Dong(Huazhong University of Science and Technology), Luo‐Qi Zhou(Huazhong University of Science and Technology), Yun‐Hui Chu(Huazhong University of Science and Technology), Xiao‐Wei Pang(Huazhong University of Science and Technology), Jiayi He(Huazhong University of Science and Technology), Ke Shang(Huazhong University of Science and Technology), Jun Xiao(Huazhong University of Science and Technology), Li Zhu(Tongji Hospital), Huan Ye(Integrated BioTherapeutics (United States)), Song-Bai Cai(Integrated BioTherapeutics (United States)), Di Wang(Tongji Hospital), Bi-Tao Bu(Huazhong University of Science and Technology), Gerd Meyer zu Hörste(University Hospital Münster), Chunrui Li(Tongji Hospital), Dai‐Shi Tian(Huazhong University of Science and Technology), Wei Wang(Huazhong University of Science and Technology)
Cell
October 15, 2025
Cited by 23Open Access
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Abstract

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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