Author:
Odak Ivan,Bayir Lâle M.,Riemann Lennart,Sikora Ruth,Schneider Jessica,Xiao Yankai,Möhn Nora,Skripuletz Thomas,Beutel Gernot,Eder Matthias,Ganser Arnold,Förster Reinhold,Schultze-Florey Christian R.,Koenecke Christian
Abstract
Variability or stability might have an impact on treatment success and toxicity of CD19 CAR T-cells. We conducted a prospective observational study of 12 patients treated with Tisagenlecleucel for CD19+ B-cell malignancies. Using a 31-color spectral flow cytometry panel, we analyzed differentiation stages and exhaustion markers of CAR T-cell subsets prior to CAR T-cell infusion and longitudinally during 6 months of follow-up. The majority of activation markers on CAR T-cells showed stable expression patterns over time and were not associated with response to therapy or toxicity. Unsupervised cluster analysis revealed an immune signature of CAR T-cell products associated with the development of immune cell-associated neurotoxicity syndrome. Warranting validation in an independent patient cohort, in-depth phenotyping of CAR T-cell products as well as longitudinal monitoring post cell transfer might become a valuable tool to increase efficacy and safety of CAR T-cell therapy.
Funder
Deutsche Forschungsgemeinschaft
Bundesministerium für Bildung und Forschung
Cited by
1 articles.
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