Brief research report: in-depth immunophenotyping reveals stability of CD19 CAR T-cells over time

Ivan Odak,Lale M. Bayir, Lennart Riemann, Ruth Sikora, Jessica Schneider,Yankai Xiao,Nora Moehn,Thomas Skripuletz, Gernot Beutel, Matthias Eder, Arnold Ganser,Reinhold Foerster,Christian R. Schultze-Florey,Christian Koenecke

FRONTIERS IN IMMUNOLOGY(2024)

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摘要
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.
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关键词
CAR T-cell,DLBCL diffuse large B-cell lymphoma,ALL acute lymphoblastic leukemia,tisagenlecleucel tisa-cel,spectral flow cytometry,immunophenotyping,CRS cytokine release syndrome,ICANS immune effector cell associated neurotoxicity syndrome
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