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Brief research report: in-depth immunophenotyping reveals stability of CD19 CAR T-cells over time.
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.
  • Odak I; Institute of Immunology, Hannover Medical School, Hannover, Germany.
  • Bayir LM; Institute of Immunology, Hannover Medical School, Hannover, Germany.
  • Riemann L; Department of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
  • Sikora R; Institute of Immunology, Hannover Medical School, Hannover, Germany.
  • Schneider J; Department of Pediatric Pneumology, Allergology and Neonatology, Hannover Medical School, Hannover, Germany.
  • Xiao Y; Institute of Immunology, Hannover Medical School, Hannover, Germany.
  • Möhn N; Department of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
  • Skripuletz T; Institute of Immunology, Hannover Medical School, Hannover, Germany.
  • Beutel G; Department of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
  • Eder M; Institute of Immunology, Hannover Medical School, Hannover, Germany.
  • Ganser A; Department of Neurology, Hannover Medical School, Hannover, Germany.
  • Förster R; Department of Neurology, Hannover Medical School, Hannover, Germany.
  • Schultze-Florey CR; Department of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
  • Koenecke C; Department of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
Front Immunol ; 15: 1298598, 2024.
Article en En | MEDLINE | ID: mdl-38318174
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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Inmunofenotipificación / Proteínas Adaptadoras Transductoras de Señales Tipo de estudio: Observational_studies Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Inmunofenotipificación / Proteínas Adaptadoras Transductoras de Señales Tipo de estudio: Observational_studies Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article