• 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

基于TCR的肝细胞癌细胞免疫疗法:进展、挑战与前景

TCR-based cellular immunotherapy for hepatocellular carcinoma: advances, challenges, and prospects.

作者信息

Zeng Wanting, Zhu Wei, Yuan Guosheng, Chen Jinzhang, Wang Zhanhui, Hou Jinlin, Jiang De-Ke

机构信息

State Key Laboratory of Organ Failure Research, Key Laboratory of Infectious Diseases Research in South China, Ministry of Education; Guangdong Provincial Key Laboratory for Prevention and Control of Major Liver Diseases, Guangdong Provincial Clinical Research Center for Viral Hepatitis, Guangdong Institute of Hepatology, Guangdong Provincial Research Center for Liver Fibrosis Engineering and Technology, Department of Infectious Diseases and Hepatology Unit, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.

The Key Laboratory of Molecular Pathology (Hepatic Diseases) of Guangxi, Department of Pathology, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, China.

出版信息

Cancer Immunol Immunother. 2025 Jul 1;74(8):257. doi: 10.1007/s00262-025-04122-z.

DOI:10.1007/s00262-025-04122-z
PMID:40590989
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12214192/
Abstract

Hepatocellular carcinoma (HCC) ranks among the most prevalent malignant tumors globally. However, current frontline treatment modalities fail to achieve satisfactory therapeutic outcomes. In recent years, T-cell receptor (TCR)-T therapy has garnered increasing attention as a promising therapeutic approach. This review provides an overview of the epidemiology of HCC, evaluates the efficacy of current first-line treatment options, and introduces adoptive cellular therapies (ACTs), with a specific focus on TCR-T therapy. Notably, we categorize existing TCR-T research targeting different antigens for the treatment of HCC, covering both published literature and registered clinical trials. Furthermore, we discuss the limitations of current TCR-T research and applications, while offering insights into future research directions and development prospects. In summary, this review comprehensively examines the research progress on TCR-T therapy for HCC from the perspective of antigen targeting. Although several challenges remain to be addressed, we believe that TCR-T therapy represents a promising approach for the treatment of HCC.

摘要

肝细胞癌(HCC)是全球最常见的恶性肿瘤之一。然而,目前的一线治疗方式未能取得令人满意的治疗效果。近年来,T细胞受体(TCR)-T疗法作为一种有前景的治疗方法受到越来越多的关注。本综述概述了HCC的流行病学,评估了当前一线治疗方案的疗效,并介绍了过继性细胞疗法(ACTs),特别关注TCR-T疗法。值得注意的是,我们对现有的针对不同抗原治疗HCC的TCR-T研究进行了分类,涵盖已发表的文献和注册的临床试验。此外,我们讨论了当前TCR-T研究和应用的局限性,同时对未来的研究方向和发展前景提供了见解。总之,本综述从抗原靶向的角度全面审视了TCR-T疗法治疗HCC的研究进展。尽管仍有一些挑战有待解决,但我们相信TCR-T疗法是治疗HCC的一种有前景的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3643/12214192/660a2ec92ee2/262_2025_4122_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3643/12214192/967c59a579af/262_2025_4122_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3643/12214192/660a2ec92ee2/262_2025_4122_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3643/12214192/967c59a579af/262_2025_4122_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3643/12214192/660a2ec92ee2/262_2025_4122_Fig2_HTML.jpg

相似文献

1
TCR-based cellular immunotherapy for hepatocellular carcinoma: advances, challenges, and prospects.基于TCR的肝细胞癌细胞免疫疗法:进展、挑战与前景
Cancer Immunol Immunother. 2025 Jul 1;74(8):257. doi: 10.1007/s00262-025-04122-z.
2
Human T cells engineered with an HLA-A2-restricted murine T-cell receptor targeting glypican 3 effectively control human hepatocellular carcinoma in mice.经工程改造后携带靶向磷脂酰肌醇蛋白聚糖3的HLA - A2限制性小鼠T细胞受体的人T细胞可有效控制小鼠体内的人肝细胞癌。
Hepatology. 2024 Nov 26. doi: 10.1097/HEP.0000000000001175.
3
Advancing liver cancer treatment with dual-targeting CAR-T therapy.采用双靶点嵌合抗原受体T细胞(CAR-T)疗法推进肝癌治疗
J Nanobiotechnology. 2025 Jun 24;23(1):462. doi: 10.1186/s12951-025-03512-w.
4
Ablative and non-surgical therapies for early and very early hepatocellular carcinoma: a systematic review and network meta-analysis.早期和极早期肝细胞癌的消融和非手术治疗:系统评价和网络荟萃分析。
Health Technol Assess. 2023 Dec;27(29):1-172. doi: 10.3310/GK5221.
5
Integrated system for screening tumor-specific TCRs, epitopes, and HLA subtypes using single-cell sequencing data.利用单细胞测序数据筛选肿瘤特异性TCR、表位和HLA亚型的集成系统。
J Immunother Cancer. 2025 Jul 31;13(7):e012029. doi: 10.1136/jitc-2025-012029.
6
Serotonin receptor 5-HT as a potential target for HCC immunotherapy.血清素受体5-HT作为肝癌免疫治疗的潜在靶点。
J Immunother Cancer. 2025 Jun 23;13(6):e011088. doi: 10.1136/jitc-2024-011088.
7
Emerging Trends in Neoadjuvant Immunotherapy for Hepatocellular Carcinoma: A Focus on Liver Transplant Candidates.肝细胞癌新辅助免疫治疗的新趋势:聚焦肝移植候选者
Cancer Rep (Hoboken). 2025 Jul;8(7):e70244. doi: 10.1002/cnr2.70244.
8
Surveillance of cirrhosis for hepatocellular carcinoma: systematic review and economic analysis.肝细胞癌肝硬化监测:系统评价与经济分析
Health Technol Assess. 2007 Sep;11(34):1-206. doi: 10.3310/hta11340.
9
Obecabtagene autoleucel, a novel CD19-directed CAR T-cell therapy for relapsed/refractory B-cell acute lymphoblastic leukemia: the future for reducing toxicity and T-cell exhaustion?奥贝卡他基因自体白细胞介素,一种用于复发/难治性B细胞急性淋巴细胞白血病的新型CD19导向嵌合抗原受体T细胞疗法:降低毒性和T细胞耗竭的未来希望?
Expert Rev Hematol. 2025 Jun 23. doi: 10.1080/17474086.2025.2523551.
10
CAR-T Cells Therapy in Glioblastoma: A Systematic Review on Molecular Targets and Treatment Strategies.嵌合抗原受体 T 细胞疗法治疗胶质母细胞瘤:分子靶点和治疗策略的系统评价。
Int J Mol Sci. 2024 Jun 29;25(13):7174. doi: 10.3390/ijms25137174.

本文引用的文献

1
Nivolumab plus ipilimumab combination therapy in patients with advanced hepatocellular carcinoma previously treated with sorafenib: 5-year results from CheckMate 040.纳武利尤单抗联合伊匹单抗治疗索拉非尼治疗后晚期肝细胞癌患者:CheckMate 040 的 5 年结果。
Ann Oncol. 2024 Jun;35(6):537-548. doi: 10.1016/j.annonc.2024.03.005. Epub 2024 May 22.
2
Identification of an HLA-A*11:01-restricted neoepitope of mutant PIK3CA and its specific T cell receptors for cancer immunotherapy targeting hotspot driver mutations.鉴定突变 PIK3CA 的 HLA-A*11:01 限制性新表位及其用于针对热点驱动突变的癌症免疫治疗的特异性 T 细胞受体。
Cancer Immunol Immunother. 2024 Jun 4;73(8):150. doi: 10.1007/s00262-024-03729-y.
3
The construction of modular universal chimeric antigen receptor T (MU-CAR-T) cells by covalent linkage of allogeneic T cells and various antibody fragments.
通过同种异体T细胞与各种抗体片段的共价连接构建模块化通用嵌合抗原受体T(MU-CAR-T)细胞。
Mol Cancer. 2024 Mar 11;23(1):53. doi: 10.1186/s12943-024-01938-8.
4
Adjuvant and neoadjuvant immunotherapies in hepatocellular carcinoma.辅助和新辅助免疫疗法在肝细胞癌中的应用。
Nat Rev Clin Oncol. 2024 Apr;21(4):294-311. doi: 10.1038/s41571-024-00868-0. Epub 2024 Feb 29.
5
Four-year overall survival update from the phase III HIMALAYA study of tremelimumab plus durvalumab in unresectable hepatocellular carcinoma.III期HIMALAYA研究中,替西木单抗联合度伐利尤单抗治疗不可切除肝细胞癌的4年总生存更新情况。
Ann Oncol. 2024 May;35(5):448-457. doi: 10.1016/j.annonc.2024.02.005. Epub 2024 Feb 19.
6
Atovaquone enhances antitumor efficacy of TCR-T therapy by augmentation of ROS-induced ferroptosis in hepatocellular carcinoma.阿托伐醌通过增强 ROS 诱导的肝癌铁死亡增强 TCR-T 治疗的抗肿瘤疗效。
Cancer Immunol Immunother. 2024 Feb 13;73(3):49. doi: 10.1007/s00262-024-03628-2.
7
Cancer statistics, 2024.2024年癌症统计数据。
CA Cancer J Clin. 2024 Jan-Feb;74(1):12-49. doi: 10.3322/caac.21820. Epub 2024 Jan 17.
8
Non-invasive CT imaging biomarker to predict immunotherapy response in gastric cancer: a multicenter study.非侵入性 CT 成像生物标志物预测胃癌免疫治疗反应:一项多中心研究。
J Immunother Cancer. 2023 Nov 21;11(11):e007807. doi: 10.1136/jitc-2023-007807.
9
TScan-II: A genome-scale platform for the de novo identification of CD4 T cell epitopes.TScan-II:从头鉴定 CD4 T 细胞表位的全基因组平台。
Cell. 2023 Dec 7;186(25):5569-5586.e21. doi: 10.1016/j.cell.2023.10.024. Epub 2023 Nov 27.
10
T cell receptor therapeutics: immunological targeting of the intracellular cancer proteome.T 细胞受体疗法:细胞内癌症蛋白质组的免疫靶向治疗。
Nat Rev Drug Discov. 2023 Dec;22(12):996-1017. doi: 10.1038/s41573-023-00809-z. Epub 2023 Oct 27.