Frontiers in Immunology (Mar 2022)

Monitoring of Circulating CAR T Cells: Validation of a Flow Cytometric Assay, Cellular Kinetics, and Phenotype Analysis Following Tisagenlecleucel

  • Andreas Peinelt,
  • Andreas Peinelt,
  • Melanie Bremm,
  • Melanie Bremm,
  • Hermann Kreyenberg,
  • Hermann Kreyenberg,
  • Claudia Cappel,
  • Claudia Cappel,
  • Julia Banisharif-Dehkordi,
  • Julia Banisharif-Dehkordi,
  • Stephanie Erben,
  • Stephanie Erben,
  • Eva Rettinger,
  • Eva Rettinger,
  • Andrea Jarisch,
  • Andrea Jarisch,
  • Roland Meisel,
  • Paul-Gerhardt Schlegel,
  • Olaf Beck,
  • Gesine Bug,
  • Jan-Henning Klusmann,
  • Thomas Klingebiel,
  • Sabine Huenecke,
  • Sabine Huenecke,
  • Peter Bader,
  • Peter Bader

DOI
https://doi.org/10.3389/fimmu.2022.830773
Journal volume & issue
Vol. 13

Abstract

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Chimeric antigen receptor (CAR) T cell therapy is a potent new treatment option for relapsed or refractory hematologic malignancies. As the monitoring of CAR T cell kinetics can provide insights into the activity of the therapy, appropriate CAR T cell detection methods are essential. Here, we report on the comprehensive validation of a flow cytometric assay for peripheral blood CD19 CAR T cell detection. Further, a retrospective analysis (n = 30) of CAR T cell and B cell levels over time has been performed, and CAR T cell phenotypes have been characterized. Serial dilution experiments demonstrated precise and linear quantification down to 0.05% of T cells or 22 CAR T cell events. The calculated detection limit at 13 events was confirmed with CAR T cell negative control samples. Inter-method comparison with real-time PCR showed appreciable correlation. Stability testing revealed diminished CAR T cell values already one day after sample collection. While we found long-term CAR T cell detectability and B cell aplasia in most patients (12/17), some patients (5/17) experienced B cell recovery. In three of these patients the coexistence of CAR T cells and regenerating B cells was observed. Repeat CAR T cell infusions led to detectable but limited re-expansions. Comparison of CAR T cell subsets with their counterparts among all T cells showed a significantly higher percentage of effector memory T cells and a significantly lower percentage of naïve T cells and T EMRA cells among CAR T cells. In conclusion, flow cytometric CAR T cell detection is a reliable method to monitor CAR T cells if measurements start without delay and sufficient T cell counts are given.

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