• 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

嵌合抗原受体 T 细胞疗法治疗 B 细胞血液系统恶性肿瘤后的复发机制及治疗策略。

Relapse Mechanism and Treatment Strategy After Chimeric Antigen Receptor T-Cell Therapy in Treating B-Cell Hematological Malignancies.

机构信息

The First Central Clinical College of Tianjin Medical University, Tianjin, China.

Department of Hematology, 66571Tianjin First Central Hospital, Tianjin, China.

出版信息

Technol Cancer Res Treat. 2022 Jan-Dec;21:15330338221118413. doi: 10.1177/15330338221118413.

DOI:10.1177/15330338221118413
PMID:35989682
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9403467/
Abstract

Over the past few decades, immunotherapy has revolutionized the modern medical oncology field. Chimeric antigen receptor (CAR)-T cell therapy has a promising curative effect in the treatment of hematological malignancies. Anti-CD19 CAR-T cells are the most mature CAR-T cells recently studied and in recent years it has achieved a complete remission rate of approximately 90% in the treatment of B-cell acute lymphoblastic leukemia (B-ALL). Although CAR-T cell therapy has greatly alleviated the disease in patients with leukemia or lymphoma, some of them still relapse after treatment. Therefore, in this article, we discuss the factors that may contribute to disease relapse following CAR-T cell therapy and summarize potential strategies to overcome these obstacles, thus providing the possibility of improving standard treatment regimens.

摘要

在过去的几十年中,免疫疗法彻底改变了现代医学肿瘤学领域。嵌合抗原受体 (CAR)-T 细胞疗法在治疗血液系统恶性肿瘤方面具有有前景的疗效。抗 CD19 CAR-T 细胞是最近研究的最成熟的 CAR-T 细胞,近年来在治疗 B 细胞急性淋巴细胞白血病 (B-ALL) 方面已达到约 90%的完全缓解率。尽管 CAR-T 细胞疗法极大地缓解了白血病或淋巴瘤患者的疾病,但其中一些患者在治疗后仍会复发。因此,在本文中,我们讨论了可能导致 CAR-T 细胞治疗后疾病复发的因素,并总结了克服这些障碍的潜在策略,从而为改善标准治疗方案提供了可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95c/9403467/1b9da1f20fe4/10.1177_15330338221118413-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95c/9403467/a16246a2db05/10.1177_15330338221118413-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95c/9403467/342b6bf9251b/10.1177_15330338221118413-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95c/9403467/1b9da1f20fe4/10.1177_15330338221118413-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95c/9403467/a16246a2db05/10.1177_15330338221118413-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95c/9403467/342b6bf9251b/10.1177_15330338221118413-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95c/9403467/1b9da1f20fe4/10.1177_15330338221118413-fig3.jpg

相似文献

1
Relapse Mechanism and Treatment Strategy After Chimeric Antigen Receptor T-Cell Therapy in Treating B-Cell Hematological Malignancies.嵌合抗原受体 T 细胞疗法治疗 B 细胞血液系统恶性肿瘤后的复发机制及治疗策略。
Technol Cancer Res Treat. 2022 Jan-Dec;21:15330338221118413. doi: 10.1177/15330338221118413.
2
Clinical development of chimeric antigen receptor-T cell therapy for hematological malignancies.嵌合抗原受体-T 细胞疗法治疗血液系统恶性肿瘤的临床进展。
Chin Med J (Engl). 2023 Oct 5;136(19):2285-2296. doi: 10.1097/CM9.0000000000002549.
3
CAR-T cell therapy in hematological malignancies: Where are we now and where are we heading for?嵌合抗原受体 T 细胞疗法在血液系统恶性肿瘤中的应用:我们现在在哪里,我们的目标在哪里?
Eur J Haematol. 2024 Jan;112(1):6-18. doi: 10.1111/ejh.14076. Epub 2023 Aug 7.
4
Clinical determinants of relapse following CAR-T therapy for hematologic malignancies: Coupling active strategies to overcome therapeutic limitations.血液系统恶性肿瘤 CAR-T 治疗后复发的临床决定因素:将主动策略与克服治疗限制相结合。
Curr Res Transl Med. 2022 Jan;70(1):103320. doi: 10.1016/j.retram.2021.103320. Epub 2021 Nov 9.
5
Recent findings on chimeric antigen receptor (CAR)-engineered immune cell therapy in solid tumors and hematological malignancies.近期关于嵌合抗原受体(CAR)修饰免疫细胞治疗实体瘤和血液恶性肿瘤的研究进展。
Stem Cell Res Ther. 2022 Sep 24;13(1):482. doi: 10.1186/s13287-022-03163-w.
6
Chimeric Antigen Receptor T Cell Exhaustion during Treatment for Hematological Malignancies.嵌合抗原受体 T 细胞耗竭在血液系统恶性肿瘤治疗期间。
Biomed Res Int. 2020 Oct 23;2020:8765028. doi: 10.1155/2020/8765028. eCollection 2020.
7
Strategies to optimize chimeric antigen receptor T-cell therapy in hematologic malignancies: Chinese experience.优化血液系统恶性肿瘤嵌合抗原受体 T 细胞治疗的策略:中国经验。
Haematologica. 2023 Aug 1;108(8):2011-2028. doi: 10.3324/haematol.2022.282316.
8
Genetic Mechanism of Leukemia Relapse Following CD19 Chimeric Antigen Receptor T Cell Therapy.CD19 嵌合抗原受体 T 细胞治疗后白血病复发的遗传机制。
Cancer Biother Radiopharm. 2022 Jun;37(5):335-341. doi: 10.1089/cbr.2020.4630. Epub 2021 Mar 18.
9
Chimeric Antigen Receptor T Cell Therapy for Pediatric B-ALL: Narrowing the Gap Between Early and Long-Term Outcomes.嵌合抗原受体 T 细胞疗法治疗小儿 B-ALL:缩小早期和长期结局之间的差距。
Front Immunol. 2020 Aug 11;11:1985. doi: 10.3389/fimmu.2020.01985. eCollection 2020.
10
Progress on CAR-T cell therapy for hematological malignancies.嵌合抗原受体 T 细胞疗法治疗血液系统恶性肿瘤的研究进展。
Zhejiang Da Xue Xue Bao Yi Xue Ban. 2022 Apr 25;51(2):192-203. doi: 10.3724/zdxbyxb-2022-0055.

引用本文的文献

1
Unveiling the potential of CLL-1: a promising target for AML therapy.揭示CLL-1的潜力:急性髓系白血病治疗的一个有前景的靶点。
Biomark Res. 2025 Feb 12;13(1):28. doi: 10.1186/s40364-025-00738-6.
2
Combination of CAR‑T cell therapy and radiotherapy: Opportunities and challenges in solid tumors (Review).嵌合抗原受体T细胞疗法与放射疗法的联合:实体瘤治疗中的机遇与挑战(综述)
Oncol Lett. 2023 May 16;26(1):281. doi: 10.3892/ol.2023.13867. eCollection 2023 Jul.
3
Bicistronic CAR-T cells targeting CD123 and CLL1 for AML to reduce the risk of antigen escape.

本文引用的文献

1
Optimization of metabolism to improve efficacy during CAR-T cell manufacturing.优化代谢以提高 CAR-T 细胞生产中的疗效。
J Transl Med. 2021 Dec 7;19(1):499. doi: 10.1186/s12967-021-03165-x.
2
Corrigendum to <Does lineage plasticity enable escape from CAR-T cell therapy? Lessons from MLL-r leukemia'>: <[Experimental Hematology 2021; 100: 1-11]>.《<谱系可塑性是否能使肿瘤细胞逃避嵌合抗原受体T细胞疗法?来自MLL-r白血病的教训>》勘误:[《实验血液学》2021年;第100卷:第1 - 11页]
Exp Hematol. 2021 Nov;103:73-74. doi: 10.1016/j.exphem.2021.09.002. Epub 2021 Sep 21.
3
PD-1/PD-L1 Checkpoint Inhibitors in Tumor Immunotherapy.
用于急性髓系白血病的靶向CD123和CLL1的双顺反子嵌合抗原受体T细胞,以降低抗原逃逸风险。
Transl Oncol. 2023 Aug;34:101695. doi: 10.1016/j.tranon.2023.101695. Epub 2023 May 22.
肿瘤免疫治疗中的PD-1/PD-L1检查点抑制剂
Front Pharmacol. 2021 Sep 1;12:731798. doi: 10.3389/fphar.2021.731798. eCollection 2021.
4
Hypermethylation of CD19 promoter enables antigen-negative escape to CART-19 in vivo and in vitro.CD19 启动子的超甲基化使得 CART-19 在体内和体外逃避抗原阴性。
J Immunother Cancer. 2021 Aug;9(8). doi: 10.1136/jitc-2021-002352.
5
Early-phenotype CAR-T cells for the treatment of pediatric cancers.用于治疗儿科癌症的早期表型 CAR-T 细胞。
Ann Oncol. 2021 Nov;32(11):1366-1380. doi: 10.1016/j.annonc.2021.07.018. Epub 2021 Aug 8.
6
CD19/CD22 Dual-Targeted CAR T-cell Therapy for Relapsed/Refractory Aggressive B-cell Lymphoma: A Safety and Efficacy Study.CD19/CD22 双靶点 CAR T 细胞治疗复发/难治性侵袭性 B 细胞淋巴瘤:一项安全性和有效性研究。
Cancer Immunol Res. 2021 Sep;9(9):1061-1070. doi: 10.1158/2326-6066.CIR-20-0675. Epub 2021 Jul 21.
7
Immune checkpoint inhibitors in lymphoma: challenges and opportunities.淋巴瘤中的免疫检查点抑制剂:挑战与机遇
Ann Transl Med. 2021 Jun;9(12):1037. doi: 10.21037/atm-20-6833.
8
Anti-CD22 CAR-T Cell Therapy as a Salvage Treatment in B Cell Malignancies Refractory or Relapsed After Anti-CD19 CAR-T therapy.抗CD22嵌合抗原受体T细胞疗法作为抗CD19嵌合抗原受体T细胞疗法难治或复发的B细胞恶性肿瘤的挽救治疗方法。
Onco Targets Ther. 2021 Jul 2;14:4023-4037. doi: 10.2147/OTT.S312904. eCollection 2021.
9
Ciltacabtagene autoleucel, a B-cell maturation antigen-directed chimeric antigen receptor T-cell therapy in patients with relapsed or refractory multiple myeloma (CARTITUDE-1): a phase 1b/2 open-label study.西达基奥仑赛,一种针对 B 细胞成熟抗原的嵌合抗原受体 T 细胞疗法,用于治疗复发或难治性多发性骨髓瘤患者(CARTITUDE-1):一项 1b/2 期开放标签研究。
Lancet. 2021 Jul 24;398(10297):314-324. doi: 10.1016/S0140-6736(21)00933-8. Epub 2021 Jun 24.
10
Taking a BiTE out of the CAR T space race.从 CAR T 空间竞赛中取出 BiTE。
Br J Haematol. 2021 Dec;195(5):689-697. doi: 10.1111/bjh.17622. Epub 2021 Jun 15.