TY - JOUR
T1 - CAR T cell–mediated bone marrow inflammation causes hematotoxicity and favors clonal hematopoiesis
AU - Khelil, Myriam Ben
AU - Arbab, Ahmadreza
AU - Srikanthan, Janesa
AU - Kovandzic, Laura Marcos
AU - Vergé, Véronique
AU - Pagès, Arnaud
AU - Rengassamy, Jessica
AU - Amine-Hneineh, Roula
AU - Aglave, Marine
AU - Jelin, Rémy
AU - Ribrag, Vincent
AU - Rahali, Wassila
AU - Goutebroze, Paul Auguste
AU - de Botton, Stéphane
AU - Menger, Laurie
AU - Antony-Debré, Ileana
AU - Micol, Jean Baptiste
AU - Marzac, Christophe
AU - Llorente, Cristina Castilla
AU - Bigenwald, Camille
N1 - Publisher Copyright:
Copyright © 2025 The Authors, some rights reserved.
PY - 2025/9/24
Y1 - 2025/9/24
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/105016909585
U2 - 10.1126/scitranslmed.adu9790
DO - 10.1126/scitranslmed.adu9790
M3 - Article
C2 - 40991725
AN - SCOPUS:105016909585
SN - 1946-6234
VL - 17
JO - Science Translational Medicine
JF - Science Translational Medicine
IS - 817
M1 - eadu9790
ER -