Pérez-Amill Lorena, Armand-Ugón Mercedes, Val-Casals Maria, Martín-Herreros Beatriz, Álamo José R, Peña Sergio, Frigola Gerard, Altuna Ane, Santos Claudio, Guijarro Francesca, Minguela Alfredo, Bataller Àlex, Casanovas-Albertí Berta, Uribe-Herranz Mireia, Navarro Irene, Guerreiro Manuel, Sánchez-Martínez Diego, Tirado Néstor, Velasco-Hernandez Talía, Menéndez Pablo, Martínez Antonio, Rovira Montse, Colomer Dolors, González-Navarro E Azucena, Esteve Jordi, Urbano-Ispizua Álvaro, Montesinos Pau, Delgado Julio, Juan Manel, Klein-González Nela
Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Gyala Therapeutics S.L., Barcelona, Spain.
Leukemia. 2025 Aug 6. doi: 10.1038/s41375-025-02705-4.
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).
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的临床成功,但在其他适应症中尚未取得类似的成果。对于复发或难治性(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细胞疗法为满足这一未满足的需求提供了巨大潜力。在此,我们介绍一种针对新型抗原CD84的一流CAR T细胞疗法,用于治疗R/R AML和T-ALL。CD84在白血病原始细胞上高度表达,在造血干祖细胞(HSPC)上表达有限,在健康人体组织中基本不存在。我们针对CD84的第二代CAR(CART84)在患者来源的异种移植(PDX)模型中,在体外和体内均对AML和T-ALL细胞表现出强大的细胞毒性。此外,CART84在体外和体内人源化小鼠模型中消除了原发性白血病原始细胞,同时对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的一个有前景的靶点,并为我们即将开展的针对R/R AML和T-ALL患者使用CD84导向的CAR T细胞疗法的首次人体I/II期临床试验(EudraCT 2024-519966-31-00)奠定了基础。