TY - JOUR
T1 - Brief research report
T2 - in-depth immunophenotyping reveals stability of CD19 CAR T-cells over time
AU - Odak, Ivan
AU - Bayir, Lâle M.
AU - Riemann, Lennart
AU - Sikora, Ruth
AU - Schneider, Jessica
AU - Xiao, Yankai
AU - Möhn, Nora
AU - Skripuletz, Thomas
AU - Beutel, Gernot
AU - Eder, Matthias
AU - Ganser, Arnold
AU - Förster, Reinhold
AU - Schultze-Florey, Christian R.
AU - Koenecke, Christian
N1 - Publisher Copyright:
Copyright © 2024 Odak, Bayir, Riemann, Sikora, Schneider, Xiao, Möhn, Skripuletz, Beutel, Eder, Ganser, Förster, Schultze-Florey and Koenecke.
PY - 2024
Y1 - 2024
N2 - 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.
AB - 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.
KW - ALL acute lymphoblastic leukemia
KW - CAR T-cell
KW - CRS cytokine release syndrome
KW - DLBCL diffuse large B-cell lymphoma
KW - ICANS immune effector cell associated neurotoxicity syndrome
KW - immunophenotyping
KW - spectral flow cytometry
KW - tisagenlecleucel tisa-cel
UR - http://www.scopus.com/inward/record.url?scp=85184154360&partnerID=8YFLogxK
U2 - 10.3389/fimmu.2024.1298598
DO - 10.3389/fimmu.2024.1298598
M3 - Article
C2 - 38318174
AN - SCOPUS:85184154360
SN - 1664-3224
VL - 15
JO - Frontiers in Immunology
JF - Frontiers in Immunology
M1 - 1298598
ER -