CD19 CAR T-Cell Therapy in Autoimmune Disease — A Case Series with Follow-up

Fabian Müller(Maine Farmland Trust), Jule Taubmann(Maine Farmland Trust), Laura Bucci(Maine Farmland Trust), Artur Wilhelm(Maine Farmland Trust), Christina Bergmann(Maine Farmland Trust), Simon Völkl(Maine Farmland Trust), Michael Aigner(Maine Farmland Trust), Tobias Rothe(Maine Farmland Trust), Ioanna Minopoulou(Maine Farmland Trust), Carlo Tur(Università Cattolica del Sacro Cuore), Johannes Knitza(Maine Farmland Trust), Soraya Kharboutli(Maine Farmland Trust), Sascha Kretschmann(Maine Farmland Trust), Ingrid Vášová(Maine Farmland Trust), Silvia Spoerl(Maine Farmland Trust), Hannah Reimann(Maine Farmland Trust), Luis E. Muñoz(Maine Farmland Trust), Roman G. Gerlach(Universitätsklinikum Erlangen), Simon Schäfer(Maine Farmland Trust), Ricardo Grieshaber‐Bouyer(Maine Farmland Trust), Anne‐Sophie Korganow(Maine Farmland Trust), Dominique Farge(Université Paris Cité), Dimitrios Mougiakakos(Maine Farmland Trust), Aline Bözec(Maine Farmland Trust), Thomas Winkler(Maine Farmland Trust), Gerhard Krönke(Maine Farmland Trust), Andréas Mackensen(Maine Farmland Trust), Georg Schett(Università Cattolica del Sacro Cuore)
New England Journal of Medicine
February 21, 2024
Cited by 897

Abstract

BACKGROUND: Treatment for autoimmune diseases such as systemic lupus erythematosus (SLE), idiopathic inflammatory myositis, and systemic sclerosis often involves long-term immune suppression. Resetting aberrant autoimmunity in these diseases through deep depletion of B cells is a potential strategy for achieving sustained drug-free remission. METHODS: We evaluated 15 patients with severe SLE (8 patients), idiopathic inflammatory myositis (3 patients), or systemic sclerosis (4 patients) who received a single infusion of CD19 chimeric antigen receptor (CAR) T cells after preconditioning with fludarabine and cyclophosphamide. Efficacy up to 2 years after CAR T-cell infusion was assessed by means of Definition of Remission in SLE (DORIS) remission criteria, American College of Rheumatology-European League against Rheumatism (ACR-EULAR) major clinical response, and the score on the European Scleroderma Trials and Research Group (EUSTAR) activity index (with higher scores indicating greater disease activity), among others. Safety variables, including cytokine release syndrome and infections, were recorded. RESULTS: The median follow-up was 15 months (range, 4 to 29). The mean (±SD) duration of B-cell aplasia was 112±47 days. All the patients with SLE had DORIS remission, all the patients with idiopathic inflammatory myositis had an ACR-EULAR major clinical response, and all the patients with systemic sclerosis had a decrease in the score on the EUSTAR activity index. Immunosuppressive therapy was completely stopped in all the patients. Grade 1 cytokine release syndrome occurred in 10 patients. One patient each had grade 2 cytokine release syndrome, grade 1 immune effector cell-associated neurotoxicity syndrome, and pneumonia that resulted in hospitalization. CONCLUSIONS: In this case series, CD19 CAR T-cell transfer appeared to be feasible, safe, and efficacious in three different autoimmune diseases, providing rationale for further controlled clinical trials. (Funded by Deutsche Forschungsgemeinschaft and others.).


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