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靶向 CD84 的新型 CAR-T 细胞疗法治疗急性髓系和 T 细胞淋巴母细胞白血病

英文原题:A novel chimeric antigen receptor T-cell therapy targeting CD84 for the treatment of acute myeloid and T-cell lymphoblastic leukemias.

查看英文原题

A novel chimeric antigen receptor T-cell therapy targeting CD84 for the treatment of acute myeloid and T-cell lymphoblastic leukemias.

PubMed 2025/08/06(内容时间) Leukemia Q1 · IF 8.8(JCR 2025)

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中文摘要

尽管嵌合抗原受体(CAR)T细胞疗法在治疗B细胞恶性肿瘤和多发性骨髓瘤方面取得了显著临床成功,但在其他适应症中尚未取得类似结果。对于复发/难治性(R/R)急性髓系白血病(AML)或T细胞急性淋巴细胞白血病(T-ALL)患者,治疗选择有限,而CAR-T 细胞疗法为解决这一未满足需求提供了巨大潜力。

在此,我们介绍一种首创的靶向CD84的CAR-T 细胞疗法,CD84是一种新型抗原,用于治疗R/R AML和T-ALL。CD84在白血病原始细胞上高表达,在造血干祖细胞(HSPC)上表达有限,并且在健康人体组织中基本缺失。

我们靶向CD84的第二代CAR-T(CAR-T84)在体外以及患者来源异种移植(PDX)模型的体内均显示出对AML和T-ALL细胞的有效细胞毒性。

此外,CAR-T84清除了原代白血病原始细胞,同时在体外和体内人源化小鼠模型中对CD34+ HSPC表现出低细胞毒性,提示骨髓毒性风险较低。这些结果支持CD84作为AML和T-ALL的有前景靶点,并为我们即将开展的首次人体I/II期临床试验奠定了基础,该试验使用CD84导向的CAR-T 细胞疗法治疗R/R AML和T-ALL患者(EudraCT 2024-519966-31-00)。

展开英文摘要原文

Despite the remarkable clinical successes of chimeric antigen receptor (CAR) T-cell therapies in treating B-cell malignancies and multiple myeloma, similar outcomes have not been achieved in other indications. For patients with relapsed or refractory (R/R) acute myeloid leukemia (AML) or T-cell acute lymphoblastic leukemia (T-ALL), treatment options are limited, yet CART-cell therapies offer significant potential to address this unmet need.

Here, we introduce a first-in-class CART-cell therapy targeting CD84, a novel antigen, for the treatment of R/R AML and T-ALL. CD84 is highly expressed on leukemic blasts, with limited expression on hematopoietic stem progenitor cells (HSPC), and is largely absent in healthy human tissues.

Our second-generation CARTs targeting CD84 (CART84) demonstrate potent cytotoxicity against AML and T-ALL cells both in vitro and in vivo in patient-derived xenograft (PDX) models.

Furthermore, CART84 eliminated primary leukemic blasts while exhibiting low cytotoxicity against CD34+ HSPC in vitro and in humanized mouse models in vivo, suggesting a low risk of myelotoxicity. These results support CD84 as a promising target for AML and T-ALL and provide the foundation for our upcoming first-in-human phase I/II clinical trial using CD84-directed CAR T cell therapy for patients with R/R AML and T-ALL (EudraCT 2024-519966-31-00).

论文信息

作者
Pérez-Amill L、Armand-Ugón M、Val-Casals M、Martín-Herreros B、Álamo JR、Peña S、Frigola G、Altuna A
第一作者单位
Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.Spain
通讯作者单位
Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain. Klein@recerca.clinic.cat.Spain
文献类型
非美国政府资助研究
期刊
Leukemia2025 Oct
原文标识
PubMed 40770072 · DOI 10.1038/s41375-025-02705-4