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

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

Research output: Contribution to journalArticlepeer-review

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.

Original languageEnglish
Article number1298598
JournalFrontiers in Immunology
Volume15
DOIs
StatePublished - 2024
Externally publishedYes

Keywords

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

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