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CAR-T 细胞介导的骨髓炎症导致血液毒性并促进克隆性造血

英文原题:CAR T cell-mediated bone marrow inflammation causes hematotoxicity and favors clonal hematopoiesis.

查看英文原题

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

PubMed 2025/09/24(内容时间) Sci Transl Med Q1 · IF 15.6(JCR 2025)

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中文摘要

尽管嵌合抗原受体(CAR)T细胞治疗血液系统恶性肿瘤效果显著,但也会引起副作用。接受CAR-T 治疗的患者可能发生持续性血细胞减少或血液毒性。本研究采用免疫功能完整的小鼠模型重现血液毒性,并证明单独使用淋巴细胞清除方案不足以诱发血液毒性,必须同时注射CAR-T 细胞。对发生血液毒性患者的骨髓(BM)样本分析显示,骨髓CAR-T 细胞与血液毒性严重程度相关。CAR-T 细胞呈现活化状态,导致强烈炎症。此外,我们在患者队列中观察到较高比例的克隆性造血,并发现CAR-T 细胞注射后数月内出现不同的造血克隆。本研究为血液毒性的病理生理机制提供了见解,并强调需要开展长期随访研究,以确定这种强烈骨髓炎症对克隆选择的影响。

展开英文摘要原文

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.

论文信息

作者
Ben Khelil M、Arbab A、Srikanthan J、Marcos-Kovandzic L、Vergé V、Pagès A、Rengassamy J、Amine-Hneineh R
单位
Inserm U1015, Gustave Roussy Cancer Campus, Villejuif 94800, France.France
文献类型
非美国政府资助研究
期刊
Science translational medicine2025 Sep 24
原文标识
PubMed 40991725 · DOI 10.1126/scitranslmed.adu9790