CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
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.
A novel chimeric antigen receptor T-cell therapy targeting CD84 for the treatment of acute myeloid and T-cell lymphoblastic leukemias.
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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)。
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).
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