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急性 T 细胞淋巴细胞白血病:嵌合抗原受体技术可能带来新希望。

Acute T-cell lymphoblastic leukemia: chimeric antigen receptor technology may offer a new hope.

机构信息

Department of Clinical Medicine, Hangzhou City University School of Medicine, Hangzhou, China.

Department of Pediatrics, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.

出版信息

Front Immunol. 2024 Aug 13;15:1410519. doi: 10.3389/fimmu.2024.1410519. eCollection 2024.

DOI:10.3389/fimmu.2024.1410519
PMID:39192970
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11347323/
Abstract

Acute lymphoblastic leukemia (ALL) is a prevalent malignancy affecting the hematopoietic system, encompassing both B-cell ALL (B-ALL) and T-cell ALL (T-ALL). T-ALL, characterized by the proliferation of T-cell progenitors in the bone marrow, presents significant treatment challenges, with patients often experiencing high relapse rates and poor long-term survival despite advances in chemotherapy and hematopoietic stem cell transplantation (HSCT). This review explores the pathogenesis and traditional treatment strategies of T-ALL, emphasizing the promising potential of chimeric antigen receptor (CAR) technology in overcoming current therapeutic limitations. CAR therapy, leveraging genetically modified immune cells to target leukemia-specific antigens, offers a novel and precise approach to T-ALL treatment. The review critically analyzes recent developments in CAR-T and CAR-NK cell therapies, their common targets, optimization strategies, clinical outcomes, and the associated challenges, providing a comprehensive overview of their clinical prospects in T-ALL treatment.

摘要

急性淋巴细胞白血病(ALL)是一种常见的影响造血系统的恶性肿瘤,包括 B 细胞 ALL(B-ALL)和 T 细胞 ALL(T-ALL)。T-ALL 的特征是骨髓中 T 细胞前体的增殖,尽管化疗和造血干细胞移植(HSCT)取得了进展,但患者仍经常经历高复发率和较差的长期生存。本综述探讨了 T-ALL 的发病机制和传统治疗策略,强调嵌合抗原受体(CAR)技术在克服当前治疗局限性方面的广阔前景。CAR 疗法利用基因修饰的免疫细胞靶向白血病特异性抗原,为 T-ALL 治疗提供了一种新颖而精确的方法。该综述批判性地分析了 CAR-T 和 CAR-NK 细胞疗法的最新进展、它们的常见靶点、优化策略、临床结果以及相关挑战,全面概述了它们在 T-ALL 治疗中的临床前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecb1/11347323/f77a731f2dae/fimmu-15-1410519-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecb1/11347323/4a415ff62336/fimmu-15-1410519-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecb1/11347323/0e7859127909/fimmu-15-1410519-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecb1/11347323/f77a731f2dae/fimmu-15-1410519-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecb1/11347323/4a415ff62336/fimmu-15-1410519-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecb1/11347323/0e7859127909/fimmu-15-1410519-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecb1/11347323/f77a731f2dae/fimmu-15-1410519-g003.jpg

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An Anti-CD7 Antibody-Drug Conjugate Target Showing Potent Antitumor Activity for T-Lymphoblastic Leukemia (T-ALL).一种针对 T 淋巴细胞白血病(T-ALL)的靶向 CD7 的抗体药物偶联物,具有强大的抗肿瘤活性。
Biomolecules. 2024 Jan 15;14(1):106. doi: 10.3390/biom14010106.
2
Chimeric Antigen Cytotoxic Receptors for In Vivo Engineering of Tumor-Targeting NK Cells.嵌合抗原细胞毒性受体用于体内工程化肿瘤靶向 NK 细胞。
Immunohorizons. 2024 Jan 1;8(1):97-105. doi: 10.4049/immunohorizons.2300099.
3
A Review of Acute Lymphocytic Leukemia (ALL) in the Pediatric Population: Evaluating Current Trends and Changes in Guidelines in the Past Decade.
儿科急性淋巴细胞白血病(ALL)综述:评估过去十年的当前趋势和指南变化
Cureus. 2023 Dec 4;15(12):e49930. doi: 10.7759/cureus.49930. eCollection 2023 Dec.
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Antitumor efficacy and safety of unedited autologous CD5.CAR T cells in relapsed/refractory mature T-cell lymphomas.未经编辑的自体 CD5.CAR T 细胞治疗复发/难治性成熟 T 细胞淋巴瘤的抗肿瘤疗效和安全性。
Blood. 2024 Mar 28;143(13):1231-1241. doi: 10.1182/blood.2023022204.
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Int Immunopharmacol. 2023 Nov;124(Pt A):110904. doi: 10.1016/j.intimp.2023.110904. Epub 2023 Sep 12.
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