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

2 Scopus citations

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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