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

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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Publication Details

Journal
Cell
Published
2025-10-15
DOI
https://doi.org/10.1016/j.cell.2025.09.020
Citations
13
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
13.59
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article

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

Song-Bai Cai, Chunrui Li, Luo‐Qi Zhou, Xiao‐Wei Pang et al.
13 citations
Cell
CAR-T cell therapy research
13.59
article

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

Song-Bai Cai, Chunrui Li, Luo‐Qi Zhou, Xiao‐Wei Pang, Ming‐Hao Dong, Yun‐Hui Chu, Chuan Qin, Bi-Tao Bu, Jun Xiao, Dai‐Shi Tian, Gerd Meyer zu Hörste, Ke Shang, Wei Wang, Di Wang, Jiayi He, Huan Ye, Li Zhu
article en
13 citations

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.

CellVol. 188(23)
University Hospital Münster (DE), Integrated BioTherapeutics (United States) (US), Tongji Hospital (CN), Huazhong University of Science and Technology (CN)
Openalex Percentile: Top 1%
CAR-T cell therapy research
13.59
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