• 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

血液系统恶性肿瘤的分子靶向药物联合 CAR-T 细胞治疗的进展。

Advances in molecular targeted drugs in combination with CAR-T cell therapy for hematologic malignancies.

机构信息

Department of Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou 510282, Guangdong, China.

Department of Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou 510282, Guangdong, China.

出版信息

Drug Resist Updat. 2024 May;74:101082. doi: 10.1016/j.drup.2024.101082. Epub 2024 Mar 26.

DOI:10.1016/j.drup.2024.101082
PMID:38569225
Abstract

Molecular targeted drugs and chimeric antigen receptor (CAR) T cell therapy represent specific biological treatments that have significantly improved the efficacy of treating hematologic malignancies. However, they face challenges such as drug resistance and recurrence after treatment. Combining molecular targeted drugs and CAR-T cells could regulate immunity, improve tumor microenvironment (TME), promote cell apoptosis, and enhance sensitivity to tumor cell killing. This approach might provide a dual coordinated attack on cancer cells, effectively eliminating minimal residual disease and overcoming therapy resistance. Moreover, molecular targeted drugs can directly or indirectly enhance the anti-tumor effect of CAR-T cells by inducing tumor target antigen expression, reversing CAR-T cell exhaustion, and reducing CAR-T cell associated toxic side effects. Therefore, combining molecular targeted drugs with CAR-T cells is a promising and novel tactic for treating hematologic malignancies. In this review article, we focus on analyzing the mechanism of therapy resistance and its reversal of CAR-T cell therapy resistance, as well as the synergistic mechanism, safety, and future challenges in CAR-T cell therapy in combination with molecular targeted drugs. We aim to explore the benefits of this combination therapy for patients with hematologic malignancies and provide a rationale for subsequent clinical studies.

摘要

分子靶向药物和嵌合抗原受体(CAR)T 细胞疗法代表了特定的生物治疗方法,它们显著提高了治疗血液系统恶性肿瘤的疗效。然而,它们面临着诸如药物耐药性和治疗后复发等挑战。将分子靶向药物和 CAR-T 细胞联合使用可以调节免疫、改善肿瘤微环境(TME)、促进细胞凋亡,并增强对肿瘤细胞杀伤的敏感性。这种方法可能为癌细胞提供双重协同攻击,有效消除微小残留疾病并克服治疗耐药性。此外,分子靶向药物可以通过诱导肿瘤靶抗原表达、逆转 CAR-T 细胞衰竭以及减少 CAR-T 细胞相关毒性副作用,直接或间接地增强 CAR-T 细胞的抗肿瘤作用。因此,将分子靶向药物与 CAR-T 细胞联合使用是治疗血液系统恶性肿瘤的一种有前途和新颖的策略。在这篇综述文章中,我们重点分析了 CAR-T 细胞治疗耐药性及其逆转的机制,以及 CAR-T 细胞与分子靶向药物联合使用的协同机制、安全性和未来挑战。我们旨在探讨这种联合治疗对血液系统恶性肿瘤患者的益处,并为后续的临床研究提供依据。

相似文献

1
Advances in molecular targeted drugs in combination with CAR-T cell therapy for hematologic malignancies.血液系统恶性肿瘤的分子靶向药物联合 CAR-T 细胞治疗的进展。
Drug Resist Updat. 2024 May;74:101082. doi: 10.1016/j.drup.2024.101082. Epub 2024 Mar 26.
2
Immune Cell Hacking: Challenges and Clinical Approaches to Create Smarter Generations of Chimeric Antigen Receptor T Cells.免疫细胞改造:创造更智能嵌合抗原受体 T 细胞的挑战和临床方法。
Front Immunol. 2018 Jul 31;9:1717. doi: 10.3389/fimmu.2018.01717. eCollection 2018.
3
Advances in CAR-T-cell therapy in T-cell malignancies.嵌合抗原受体 T 细胞疗法在 T 细胞恶性肿瘤中的进展。
J Hematol Oncol. 2024 Jun 24;17(1):49. doi: 10.1186/s13045-024-01568-z.
4
Befriending the Hostile Tumor Microenvironment in CAR T-Cell Therapy.CAR T 细胞疗法中与肿瘤微环境友好相处。
Front Immunol. 2021 Feb 10;11:618387. doi: 10.3389/fimmu.2020.618387. eCollection 2020.
5
T Cell Exhaustion and CAR-T Immunotherapy in Hematological Malignancies.T 细胞耗竭与嵌合抗原受体 T 细胞免疫疗法在血液系统恶性肿瘤中的应用。
Biomed Res Int. 2021 Feb 25;2021:6616391. doi: 10.1155/2021/6616391. eCollection 2021.
6
Overcoming the challenges of primary resistance and relapse after CAR-T cell therapy.克服 CAR-T 细胞治疗后原发性耐药和复发的挑战。
Expert Rev Clin Immunol. 2024 Jul;20(7):745-763. doi: 10.1080/1744666X.2024.2349738. Epub 2024 May 14.
7
The role of bone marrow microenvironment on CAR-T efficacy in haematologic malignancies.骨髓微环境对血液系统恶性肿瘤 CAR-T 疗效的影响。
Scand J Immunol. 2023 Aug;98(2):e13273. doi: 10.1111/sji.13273. Epub 2023 May 6.
8
Advances in research on factors affecting chimeric antigen receptor T-cell efficacy.嵌合抗原受体 T 细胞疗效影响因素的研究进展。
Cancer Med. 2024 Jun;13(11):e7375. doi: 10.1002/cam4.7375.
9
CAR T-Cell Therapy in Hematological Malignancies.血液系统恶性肿瘤中的嵌合抗原受体T细胞疗法
Int J Mol Sci. 2021 Aug 20;22(16):8996. doi: 10.3390/ijms22168996.
10
Dual targeting chimeric antigen receptor cells enhance antitumour activity by overcoming T cell exhaustion in pancreatic cancer.双靶点嵌合抗原受体细胞通过克服胰腺癌中的 T 细胞耗竭增强抗肿瘤活性。
Br J Pharmacol. 2024 Nov;181(22):4628-4646. doi: 10.1111/bph.16505. Epub 2024 Aug 11.

引用本文的文献

1
Advances and Challenges in Targeted Therapy and Its Combination Strategies for Leukemia.白血病靶向治疗及其联合策略的进展与挑战
Biomedicines. 2025 Jul 7;13(7):1652. doi: 10.3390/biomedicines13071652.
2
Measles Virus-Based Genetic Modifications: Progress in Hematological Malignancy Treatment.基于麻疹病毒的基因改造:血液系统恶性肿瘤治疗的进展
Onco Targets Ther. 2025 Apr 25;18:605-615. doi: 10.2147/OTT.S518407. eCollection 2025.
3
A Comprehensive Review About the Use of Monoclonal Antibodies in Cancer Therapy.关于单克隆抗体在癌症治疗中应用的综合综述。
Antibodies (Basel). 2025 Apr 11;14(2):35. doi: 10.3390/antib14020035.
4
Advances in Cell and Immune Therapies for Melanoma.黑色素瘤的细胞与免疫疗法进展
Biomedicines. 2025 Jan 3;13(1):98. doi: 10.3390/biomedicines13010098.
5
Advancing Chimeric Antigen Receptor T-Cell Therapy for Acute Myeloid Leukemia: Current Limitations and Emerging Strategies.推进嵌合抗原受体T细胞疗法治疗急性髓系白血病:当前局限与新出现的策略
Pharmaceuticals (Basel). 2024 Dec 4;17(12):1629. doi: 10.3390/ph17121629.
6
Lapatinib: A Potential Therapeutic Agent for Colon Cancer Targeting Ferroptosis.拉帕替尼:一种靶向铁死亡的结肠癌潜在治疗药物。
Anticancer Agents Med Chem. 2025;25(2):114-123. doi: 10.2174/0118715206327756240830062531.
7
Reshaping the tumor immune microenvironment to improve CAR-T cell-based cancer immunotherapy.重塑肿瘤免疫微环境以改善基于 CAR-T 细胞的癌症免疫疗法。
Mol Cancer. 2024 Aug 26;23(1):175. doi: 10.1186/s12943-024-02079-8.