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治疗急性髓系白血病的异基因双阴性 T 细胞疗法

英文原题:Allogeneic double-negative T-cell therapy for acute myeloid leukemia.

查看英文原题

Allogeneic double-negative T-cell therapy for acute myeloid leukemia.

PubMed 2025/05/10(内容时间) Curr Opin Pharmacol Q1 · IF 5.5(JCR 2025)

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中文摘要

CD3⁺CD4⁻CD8⁻双阴性T细胞(DNT)是具有独特特征的T淋巴细胞亚群,对急性髓系白血病(AML)具有强效细胞毒性。重要的是,异体DNT不会引起移植物抗宿主病,并具备适合现货型细胞治疗的特性;早期临床试验已显示出有前景的疗效。DNT治疗可与传统AML疗法协同作用,也可通过嵌合抗原受体(CAR)进行转导。值得注意的是,在获得长期缓解的患者中,持续存在的CAR⁺ T细胞主要呈DNT表型。异体DNT独特且多样的治疗特性,使其成为AML过继细胞治疗的有力候选方案。

展开英文摘要原文

CD3 + CD4 - CD8 - double-negative T cells (DNTs) represent a unique subset of T lymphocytes with potent cytotoxicity against acute myeloid leukemia (AML).

Importantly, allogeneic DNTs do not induce graft-versus-host disease and have demonstrated characteristics suitable for off-the-shelf cellular therapy with promising efficacy in early-stage clinical trials. DNT therapy can synergize with conventional AML treatments and can be transduced with chimeric antigen receptors (CARs).

Notably, persistent CAR + T cells in patients, who achieved long-term remission, predominantly have a DNT phenotype. The unique and versatile therapeutic properties of allogeneic DNTs position them as a strong candidate among adoptive cellular therapies for AML.

论文信息

作者
Tin E、Lee J、Zhang L
第一作者单位
Toronto General Hospital Research Institute, University Health Network, Toronto, Ontario, Canada; Department of Immunology, University of Toronto, Toronto, Ontario, Canada.Canada
通讯作者单位
Toronto General Hospital Research Institute, University Health Network, Toronto, Ontario, Canada; Department of Immunology, University of Toronto, Toronto, Ontario, Canada; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada. Electronic address: li.zhang@uhnresearch.ca.Canada
文献类型
综述
期刊
Current opinion in pharmacology2025 Aug
原文标识
PubMed 40441065 · DOI 10.1016/j.coph.2025.102537