BCMA-directed mRNA CAR-T cell therapy for myasthenia gravis: exploratory biomarker analysis of a placebo-controlled phase 2b trial
Summary
Chimeric antigen receptor (CAR)-T cell therapies have the potential to transform treatment of autoimmune disease by resetting the immune system. However, adoption of cell therapies in the autoimmune space is limited by hurdles such as inpatient administration, lymphodepletion and safety concerns around cytokine release syndrome and non-specific immunosuppression. RNA-based cell therapy has potential to address these limitations. Here we report prespecified exploratory analyses from a succe
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# BCMA-directed mRNA CAR-T cell therapy for myasthenia gravis: exploratory biomarker analysis of a placebo-controlled phase 2b trial
*Published: 2026 Mar*
Chimeric antigen receptor (CAR)-T cell therapies have the potential to transform
treatment of autoimmune disease by resetting the immune system. However,
adoption of cell therapies in the autoimmune space is limited by hurdles such as
inpatient administration, lymphodepletion and safety concerns around cytokine
release syndrome and non-specific immunosuppression. RNA-based cell therapy has
potential to address these limitations. Here we report prespecified exploratory
analyses from a successful placebo-controlled, double-blind, randomized phase 2b
trial in patients with generalized myasthenia gravis who received Descartes-08,
an autologous, RNA-encoded anti-B cell maturation antigen (BCMA) CAR-T cell
therapy. In 66.7% of patients (n = 10/15), transient targeting of BCMA with
Descartes-08 administered in an outpatient setting without lymphodepletion
resulted in durable clinical efficacy. Comparison of Descartes-08-treated
(n ≤ 19) and placebo (n ≤ 15) cohorts by flow cytometry, serum profiling,
multiplexing cytokine analysis and bulk/single-cell transcriptional analysis
reveals a precision retuning of self-reactivity demonstrated by increased
pro-immune function, decreased activity of BCMA+ plasma cells and plasmacytoid
dendritic cells and reductions in disease-associated cytokines, such as IL-6.
Furthermore, antibody and T cell receptor analysis revealed altered circulating
repertoires of self-reactive antibodies and T cell clones among Descartes-08
participants. These effects occurred without immune suppression, indicated by
the lack of decline in vaccine-specific antibodies or hypogammaglobulinemia. Our
findings unveil a new type of immune reset and support the development of
BCMA-targeted RNA cell therapies as a more accessible therapy for autoimmune
diseases. ClinicalTrials.gov identifier: NCT04146051 .
DOI: 10.1038/s41591-025-04170-z