• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

利用T细胞受体靶向髓系恶性肿瘤的根源。

Targeting the roots of myeloid malignancies with T cell receptors.

作者信息

Foldvari Zsofia, Brennan Margs S, Titov Aleksei, Jacobsen Sten Eirik W, Olweus Johanna

机构信息

Department of Cancer Immunology, Oslo University Hospital Radiumhospitalet, Oslo, Norway.

Precision Immunotherapy Alliance, University of Oslo, Oslo, Norway.

出版信息

Nat Rev Cancer. 2025 Aug 21. doi: 10.1038/s41568-025-00857-0.

DOI:10.1038/s41568-025-00857-0
PMID:40841587
Abstract

Myeloid malignancies are clonal diseases of haematopoietic stem cell or haematopoietic progenitor cell origin, for which allogeneic haematopoietic stem cell transplantation remains the only curative treatment for most patients. However, the severe side effects and high relapse rates underscore the need for novel therapies. The success of adoptive transfer of chimeric antigen receptor (CAR) T cells targeting B cell-specific cell surface molecules in B cell cancers has not been replicated in myeloid malignancies. T cells engineered to express cancer-directed T cell receptors (TCRs) could provide an alternative, enabling targeting also of the intracellular proteome. In this Perspective, we have collated and reviewed available data from clinical trials exploiting TCR-engineered T cells for the treatment of haematological malignancies and discuss specific characteristics that make myeloid malignancies attractive candidates for TCR-based therapies. We also highlight the need to efficiently target the rare and notoriously therapy-resistant leukaemic stem cells, which represent the roots of myeloid malignancies, to achieve cures. This will require identification of novel targets and TCRs, and we discuss different target categories and strategies that can be applied towards this goal. We also highlight the importance of standardized preclinical testing and publicly available data to enable rapid identification and clinical advancement of promising TCRs towards clinical application.

摘要

髓系恶性肿瘤是起源于造血干细胞或造血祖细胞的克隆性疾病,对于大多数患者而言,异基因造血干细胞移植仍然是唯一的治愈性治疗方法。然而,严重的副作用和高复发率凸显了新型疗法的必要性。嵌合抗原受体(CAR)T细胞靶向B细胞特异性细胞表面分子用于B细胞癌症的过继性转移取得了成功,但在髓系恶性肿瘤中尚未得到复制。经过工程改造以表达癌症导向性T细胞受体(TCR)的T细胞可能提供一种替代方案,还能够靶向细胞内蛋白质组。在这篇观点文章中,我们整理并回顾了利用TCR工程改造的T细胞治疗血液系统恶性肿瘤的临床试验现有数据,并讨论了使髓系恶性肿瘤成为基于TCR疗法有吸引力候选对象的具体特征。我们还强调了有效靶向罕见且 notoriously 难治的白血病干细胞的必要性,这些干细胞是髓系恶性肿瘤的根源,以实现治愈。这将需要鉴定新型靶点和TCR,我们讨论了可用于实现这一目标的不同靶点类别和策略。我们还强调了标准化临床前测试和公开可用数据对于快速鉴定有前景的TCR并将其推进至临床应用的重要性。 (注:notoriously 这个词在原文语境中不太明确其准确含义,这里保留英文未翻译,因为仅根据现有信息无法准确给出合适的中文表述)

相似文献

1
Targeting the roots of myeloid malignancies with T cell receptors.利用T细胞受体靶向髓系恶性肿瘤的根源。
Nat Rev Cancer. 2025 Aug 21. doi: 10.1038/s41568-025-00857-0.
2
Prescription of Controlled Substances: Benefits and Risks管制药品的处方:益处与风险
3
Restrictive versus liberal red blood cell transfusion strategies for people with haematological malignancies treated with intensive chemotherapy or radiotherapy, or both, with or without haematopoietic stem cell support.对于接受强化化疗或放疗或两者联合治疗、有或没有造血干细胞支持的血液系统恶性肿瘤患者,采用限制性与宽松性红细胞输血策略的比较。
Cochrane Database Syst Rev. 2017 Jan 27;1(1):CD011305. doi: 10.1002/14651858.CD011305.pub2.
4
Bone marrow versus peripheral blood allogeneic haematopoietic stem cell transplantation for haematological malignancies in adults.成人血液系统恶性肿瘤的骨髓与外周血异基因造血干细胞移植。
Cochrane Database Syst Rev. 2024 Nov 7;11(11):CD010189. doi: 10.1002/14651858.CD010189.pub3.
5
Chimeric antigen receptor (CAR) T-cell therapy for people with relapsed or refractory diffuse large B-cell lymphoma.嵌合抗原受体 (CAR) T 细胞疗法治疗复发或难治性弥漫性大 B 细胞淋巴瘤患者。
Cochrane Database Syst Rev. 2021 Sep 13;9(9):CD013365. doi: 10.1002/14651858.CD013365.pub2.
6
Bone marrow versus peripheral blood allogeneic haematopoietic stem cell transplantation for haematological malignancies in adults.成人血液系统恶性肿瘤的骨髓与外周血异基因造血干细胞移植
Cochrane Database Syst Rev. 2014 Apr 20;2014(4):CD010189. doi: 10.1002/14651858.CD010189.pub2.
7
The Black Book of Psychotropic Dosing and Monitoring.《精神药物剂量与监测黑皮书》
Psychopharmacol Bull. 2024 Jul 8;54(3):8-59.
8
A systematic overview of chemotherapy effects in acute myeloid leukaemia.急性髓系白血病化疗效果的系统综述。
Acta Oncol. 2001;40(2-3):231-52. doi: 10.1080/02841860151116321.
9
Metabolic reprogramming via an engineered PGC-1α improves human chimeric antigen receptor T-cell therapy against solid tumors.通过工程化 PGC-1α 进行代谢重编程可改善针对实体瘤的人嵌合抗原受体 T 细胞疗法。
J Immunother Cancer. 2023 Mar;11(3). doi: 10.1136/jitc-2022-006522.
10
Alternatives, and adjuncts, to prophylactic platelet transfusion for people with haematological malignancies undergoing intensive chemotherapy or stem cell transplantation.对于接受强化化疗或干细胞移植的血液系统恶性肿瘤患者,预防性血小板输注的替代方法和辅助措施。
Cochrane Database Syst Rev. 2016 Aug 22;2016(8):CD010982. doi: 10.1002/14651858.CD010982.pub2.

本文引用的文献

1
Bronze Age Yersinia pestis genome from sheep sheds light on hosts and evolution of a prehistoric plague lineage.来自羊舍的青铜时代鼠疫耶尔森菌基因组揭示了史前鼠疫谱系的宿主及进化情况。
Cell. 2025 Aug 7. doi: 10.1016/j.cell.2025.07.029.
2
Tumour-wide RNA splicing aberrations generate actionable public neoantigens.肿瘤全基因组RNA剪接异常产生可靶向的公共新抗原。
Nature. 2025 Mar;639(8054):463-473. doi: 10.1038/s41586-024-08552-0. Epub 2025 Feb 19.
3
Adoptive T cell therapy targeting an inducible and broadly shared product of aberrant mRNA translation.
靶向异常mRNA翻译的一种可诱导且广泛共享产物的过继性T细胞疗法。
Immunity. 2025 Jan 14;58(1):247-262.e9. doi: 10.1016/j.immuni.2024.12.004. Epub 2025 Jan 3.
4
Characterization of the Bone Marrow Lymphoid Microenvironment and Discovery of Prognostic Immune-Related Factors in Acute Myeloid Leukemia.急性髓系白血病中骨髓淋巴微环境的特征及预后免疫相关因子的发现
Int J Mol Sci. 2024 Dec 4;25(23):13039. doi: 10.3390/ijms252313039.
5
T-Switch: A specificity-based engineering platform for developing safe and effective T cell therapeutics.T转换开关:一个用于开发安全有效的T细胞疗法的基于特异性的工程平台。
Immunity. 2024 Dec 10;57(12):2945-2958.e5. doi: 10.1016/j.immuni.2024.11.009. Epub 2024 Dec 3.
6
A comprehensive proteogenomic pipeline for neoantigen discovery to advance personalized cancer immunotherapy.一种用于新抗原发现的综合蛋白质基因组学流程,以推进个性化癌症免疫治疗。
Nat Biotechnol. 2024 Oct 11. doi: 10.1038/s41587-024-02420-y.
7
Advancing CAR T-cell therapies: Preclinical insights and clinical translation for hematological malignancies.推进嵌合抗原受体 T 细胞疗法:血液系统恶性肿瘤的临床前见解与临床转化。
Blood Rev. 2024 Nov;68:101241. doi: 10.1016/j.blre.2024.101241. Epub 2024 Sep 12.
8
Enhancing cellular immunotherapies in cancer by engineering selective therapeutic resistance.通过工程化选择性治疗抵抗增强癌症的细胞免疫疗法。
Nat Rev Cancer. 2024 Sep;24(9):614-628. doi: 10.1038/s41568-024-00723-5. Epub 2024 Jul 24.
9
Molecular taxonomy of myelodysplastic syndromes and its clinical implications.骨髓增生异常综合征的分子分类及其临床意义。
Blood. 2024 Oct 10;144(15):1617-1632. doi: 10.1182/blood.2023023727.
10
Risk of Second Tumors and T-Cell Lymphoma after CAR T-Cell Therapy.CAR T 细胞治疗后第二肿瘤和 T 细胞淋巴瘤的风险。
N Engl J Med. 2024 Jun 13;390(22):2047-2060. doi: 10.1056/NEJMoa2401361.