CAR T cell–mediated bone marrow inflammation causes hematotoxicity and favors clonal hematopoiesis

  • Myriam Ben Khelil
  • , Ahmadreza Arbab
  • , Janesa Srikanthan
  • , Laura Marcos Kovandzic
  • , Véronique Vergé
  • , Arnaud Pagès
  • , Jessica Rengassamy
  • , Roula Amine-Hneineh
  • , Marine Aglave
  • , Rémy Jelin
  • , Vincent Ribrag
  • , Wassila Rahali
  • , Paul Auguste Goutebroze
  • , Stéphane de Botton
  • , Laurie Menger
  • , Ileana Antony-Debré
  • , Jean Baptiste Micol
  • , Christophe Marzac
  • , Cristina Castilla Llorente
  • , Camille Bigenwald

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Although chimeric antigen receptor (CAR) T cells have shown excellent results in treating hematological malignancies, they also cause side effects. Patients treated with CAR T cells experience persistent cytopenia or hematotox. Here, using a fully immunocompetent mouse model, we recapitulated hematotox and demonstrated that a lymphodepleting regimen alone was insufficient to induce hematotox and required CAR T cell injection. Analysis of bone marrow (BM) samples from patients experiencing hematotox revealed a correlation between BM CAR T cells and hematotox severity. CAR T cells exhibited an activated program, leading to intense inflammation. In addition, we observed a high rate of clonal hematopoiesis in our patient cohort and the emergence of distinct hematopoietic clones in the months after CAR T cell injection. Our study provides insights into the pathophysiology of hematotox and highlights the need for long-term follow-up studies to determine the relevance of this intense BM inflammation in clonal selection.

Original languageEnglish
Article numbereadu9790
JournalScience Translational Medicine
Volume17
Issue number817
DOIs
StatePublished - 24 Sep 2025
Externally publishedYes

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