CD19-targeted chimeric antigen receptor T cell therapy in two patients with multiple sclerosis

Felix Fischbach(University Medical Center Hamburg-Eppendorf), Johanna Richter(Universität Hamburg), Lena Kristina Pfeffer(Universität Hamburg), Boris Fehse(Universität Hamburg), Susanna Carolina Berger(Universität Hamburg), Stefanie Reinhardt(Universität Hamburg), Jens Kühle(University of Basel), Anita Badbaran(University Medical Center Hamburg-Eppendorf), Kristin Rathje(Universität Hamburg), Nico Gagelmann(Universität Hamburg), Dominic Borie, Johan Seibel(University Medical Center Hamburg-Eppendorf), Francis Ayuk(Universität Hamburg), Manuel A. Friese(University Medical Center Hamburg-Eppendorf), Christoph Heesen(University Medical Center Hamburg-Eppendorf), Nicolaus Kröger(University Medical Center Hamburg-Eppendorf)
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Abstract

BACKGROUND: Progressive multiple sclerosis (MS) is characterized by compartmentalized smoldering neuroinflammation caused by the proliferation of immune cells residing in the central nervous system (CNS), including B cells. Although inflammatory activity can be prevented by immunomodulatory therapies during early disease, such therapies typically fail to halt disease progression. CD19 chimeric antigen receptor (CAR)-T cell therapies have revolutionized the field of hematologic malignancies. Although generally considered efficacious, serious adverse events associated with CAR-T cell therapies such as immune effector cell-associated neurotoxicity syndrome (ICANS) have been observed. Successful use of CD19 CAR-T cells in rheumatic diseases like systemic lupus erythematosus and neuroimmunological diseases like myasthenia gravis have recently been observed, suggesting possible application in other autoimmune diseases. METHODS: Here, we report the first individual treatment with a fully human CD19 CAR-T cell therapy (KYV-101) in two patients with progressive MS. FINDINGS: CD19 CAR-T cell administration resulted in acceptable safety profiles for both patients. No ICANS was observed despite detection of CD19 CAR-T cells in the cerebrospinal fluid. In case 1, intrathecal antibody production in the cerebrospinal fluid decreased notably after CAR-T cell infusion and was sustained through day 64. CONCLUSIONS: target cells in the CNS. Larger clinical studies assessing CD19 CAR-T cells in MS are warranted. FUNDING: Both individual treatments as well the generated data were not based on external funding.


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