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A longitudinal single-cell atlas to predict outcome and toxicity after BCMA-directed CAR T cell therapy in multiple myeloma

  • Michael Rade
  • , David Fandrei
  • , Markus Kreuz
  • , Sabine Seiffert
  • , Anja Grahnert
  • , Maik Friedrich
  • , Thomas Wiemers
  • , Patrick Born
  • , Luise Fischer
  • , Heike Weidner
  • , Lorenz C. Hofbauer
  • , Ronny Baber
  • , Song Yau Wang
  • , Enrica Bach
  • , Sandra Hoffmann
  • , Jonathan Scolnick
  • , Mirco Friedrich
  • , Farid Keramati
  • , Peter Brazda
  • , Zsolt Sebestyen
  • Jürgen Kuball, Miriam Alb, Lukas Scheller, Michael Hudecek, Hermann Einsele, Klaus H. Metzeler, Marco Herling, Carmen Diana Herling, Madlen Jentzsch, Georg Nikolaus Franke, Andreas Boldt, Ulrike Köhl, Uwe Platzbecker, Vladan Vucinic, Kristin Reiche, Maximilian Merz

Onderzoeksoutput: Bijdrage aan tijdschriftArtikelpeer review

11 Citaten (Scopus)

Samenvatting

Chimeric antigen receptor (CAR) T cell therapies targeting B cell maturation antigen (BCMA) are transforming treatment for relapsed or refractory multiple myeloma (RRMM). We analyze 61 RRMM patients receiving idecabtagene vicleucel (Ide-cel; n = 34) or ciltacabtagene autoleucel (Cilta-cel; n = 27) and find that Cilta-cel achieves higher complete response (CR) rates (78% vs. 38%) and longer progression-free survival. Using a longitudinal single-cell multi-omics atlas of 135 blood samples, we show that Cilta-cel induces expansion of CD4+ cytotoxic T cells associated with CR and immune-related toxicities, whereas non-CR CD8+ T cells display impaired effector programs. Among non-B cells, plasmacytoid dendritic cells (pDCs) show the highest BCMA expression and BCMA-targeted agents eradicate a blastic plasmacytoid dendritic cell neoplasm line, suggesting a novel therapeutic avenue for this disease. Greater reductions in soluble BCMA correlate with enhanced CAR T expansion and systemic inflammation. These findings reveal cellular mechanisms driving differential efficacy and toxicity of BCMA-directed immunotherapy.

Originele taal-2Engels
Pagina's (van-tot)586-603.e9
TijdschriftCancer Cell
Volume44
Nummer van het tijdschrift3
DOI's
StatusGepubliceerd - 9 mrt 2026

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