细胞减少
骨髓
造血
炎症
嵌合抗原受体
免疫学
癌症研究
T细胞
抗原
生物
医学
免疫分型
病理生理学
受体
川地34
临床意义
克隆(Java方法)
髓外造血
癌症的体细胞进化
白血病
细胞
单克隆抗体
B细胞
T淋巴细胞
T细胞受体
作者
Myriam Ben Khelil,Ahmadreza Arbab,Janesa Srikanthan,Laura Marcos Kovandzic,Véronique Vergé,Arnaud Pagès,Jessica Rengassamy,Roula Amine-Hneineh,Marine Aglave,Rémy Jélin,Vincent Ribrag,Wassila Rahali,Paul-Auguste Goutebroze,Stéphane de Botton,Laurie Menger,Iléana Antony‐Debré,Jean-Baptiste Micol,Christophe Marzac,Cristina Castilla Llorente,Camille Bigenwald
标识
DOI:10.1126/scitranslmed.adu9790
摘要
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.
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