• 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

双特异性和三特异性T细胞衔接器武装的溶瘤病毒:新一代癌症免疫疗法

Bi- and Tri-Specific T Cell Engager-Armed Oncolytic Viruses: Next-Generation Cancer Immunotherapy.

作者信息

Guo Zong Sheng, Lotze Michael T, Zhu Zhi, Storkus Walter J, Song Xiao-Tong

机构信息

UPMC Hillman Cancer Center, Pittsburgh, PA 15213, USA.

Department of Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.

出版信息

Biomedicines. 2020 Jul 10;8(7):204. doi: 10.3390/biomedicines8070204.

DOI:10.3390/biomedicines8070204
PMID:32664210
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7400484/
Abstract

Oncolytic viruses (OVs) are potent anti-cancer biologics with a bright future, having substantial evidence of efficacy in patients with cancer. Bi- and tri-specific antibodies targeting tumor antigens and capable of activating T cell receptor signaling have also shown great promise in cancer immunotherapy. In a cutting-edge strategy, investigators have incorporated the two independent anti-cancer modalities, transforming them into bi- or tri-specific T cell engager (BiTE or TriTE)-armed OVs for targeted immunotherapy. Since 2014, multiple research teams have studied this combinatorial strategy, and it showed substantial efficacy in various tumor models. Here, we first provide a brief overview of the current status of oncolytic virotherapy and the use of multi-specific antibodies for cancer immunotherapy. We then summarize progress on BiTE and TriTE antibodies as a novel class of cancer therapeutics in preclinical and clinical studies, followed by a discussion of BiTE- or TriTE-armed OVs for cancer therapy in translational models. In addition, T cell receptor mimics (TCRm) have been developed into BiTEs and are expected to greatly expand the application of BiTEs and BiTE-armed OVs for the effective targeting of intracellular tumor antigens. Future applications of such innovative combination strategies are emerging as precision cancer immunotherapies.

摘要

溶瘤病毒(OVs)是一种具有光明前景的强效抗癌生物制剂,在癌症患者中具有大量疗效证据。靶向肿瘤抗原并能够激活T细胞受体信号传导的双特异性和三特异性抗体在癌症免疫治疗中也显示出巨大潜力。在一项前沿策略中,研究人员将这两种独立的抗癌模式结合起来,将它们转化为用于靶向免疫治疗的双特异性或三特异性T细胞衔接器(BiTE或TriTE)武装的溶瘤病毒。自2014年以来,多个研究团队对这种联合策略进行了研究,并且它在各种肿瘤模型中显示出显著疗效。在这里,我们首先简要概述溶瘤病毒疗法的现状以及多特异性抗体在癌症免疫治疗中的应用。然后,我们总结了BiTE和TriTE抗体作为一类新型癌症治疗药物在临床前和临床研究中的进展,接着讨论了在转化模型中用于癌症治疗的BiTE或TriTE武装的溶瘤病毒。此外,T细胞受体模拟物(TCRm)已被开发成BiTEs,并有望极大地扩展BiTEs和BiTE武装的溶瘤病毒对细胞内肿瘤抗原进行有效靶向的应用。这种创新联合策略的未来应用正作为精准癌症免疫疗法而出现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfa2/7400484/958f40d62208/biomedicines-08-00204-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfa2/7400484/e3b88a8079a1/biomedicines-08-00204-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfa2/7400484/1de82edb1fa1/biomedicines-08-00204-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfa2/7400484/958f40d62208/biomedicines-08-00204-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfa2/7400484/e3b88a8079a1/biomedicines-08-00204-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfa2/7400484/1de82edb1fa1/biomedicines-08-00204-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfa2/7400484/958f40d62208/biomedicines-08-00204-g003.jpg

相似文献

1
Bi- and Tri-Specific T Cell Engager-Armed Oncolytic Viruses: Next-Generation Cancer Immunotherapy.双特异性和三特异性T细胞衔接器武装的溶瘤病毒:新一代癌症免疫疗法
Biomedicines. 2020 Jul 10;8(7):204. doi: 10.3390/biomedicines8070204.
2
Revolutionizing cancer treatment: the power of bi- and tri-specific T-cell engagers in oncolytic virotherapy.革新癌症治疗:双特异性和三特异性T细胞衔接器在溶瘤病毒疗法中的力量
Front Immunol. 2024 Feb 22;15:1343378. doi: 10.3389/fimmu.2024.1343378. eCollection 2024.
3
Solid Tumor Immunotherapy with T Cell Engager-Armed Oncolytic Viruses.肿瘤免疫治疗:嵌合抗原受体 T 细胞与溶瘤病毒
Macromol Biosci. 2018 Jan;18(1). doi: 10.1002/mabi.201700187. Epub 2017 Sep 13.
4
Oncolytic viruses encoding bispecific T cell engagers: a blueprint for emerging immunovirotherapies.溶瘤病毒编码双特异性 T 细胞衔接器:新兴免疫病毒疗法的蓝图。
J Hematol Oncol. 2021 Apr 16;14(1):63. doi: 10.1186/s13045-021-01075-5.
5
Nanobody-based trispecific T cell engager (Nb-TriTE) enhances therapeutic efficacy by overcoming tumor-mediated immunosuppression.基于纳米抗体的三特异性 T 细胞衔接器(Nb-TriTE)通过克服肿瘤介导的免疫抑制来提高治疗效果。
J Hematol Oncol. 2023 Nov 29;16(1):115. doi: 10.1186/s13045-023-01507-4.
6
Bi- and tri-valent T cell engagers deplete tumour-associated macrophages in cancer patient samples.双价和三价 T 细胞衔接器在癌症患者样本中耗尽肿瘤相关巨噬细胞。
J Immunother Cancer. 2019 Nov 21;7(1):320. doi: 10.1186/s40425-019-0807-6.
7
Bispecific T cell engagers and their synergistic tumor immunotherapy with oncolytic viruses.双特异性T细胞衔接器及其与溶瘤病毒的协同肿瘤免疫疗法。
Am J Cancer Res. 2021 Jun 15;11(6):2430-2455. eCollection 2021.
8
Oncolytic herpesvirus expressing PD-L1 BiTE for cancer therapy: exploiting tumor immune suppression as an opportunity for targeted immunotherapy.表达 PD-L1 BiTE 的溶瘤单纯疱疹病毒用于癌症治疗:利用肿瘤免疫抑制作为靶向免疫治疗的机会。
J Immunother Cancer. 2021 Mar;9(4). doi: 10.1136/jitc-2020-001292.
9
[Preparation of CD33 targeted bispecific- and trispecific-T cell engagers and their cytotoxicity on leukemia cells].[CD33靶向双特异性和三特异性T细胞衔接子的制备及其对白血病细胞的细胞毒性]
Zhonghua Xue Ye Xue Za Zhi. 2022 May 14;43(5):376-382. doi: 10.3760/cma.j.issn.0253-2727.2022.05.005.
10
Targeting the tumor stroma with an oncolytic adenovirus secreting a fibroblast activation protein-targeted bispecific T-cell engager.针对肿瘤基质,使用一种分泌成纤维细胞活化蛋白靶向双特异性 T 细胞衔接子的溶瘤腺病毒。
J Immunother Cancer. 2019 Jan 25;7(1):19. doi: 10.1186/s40425-019-0505-4.

引用本文的文献

1
Immunotherapy and liver transplantation for hepatocellular carcinoma: Current and future challenges.肝细胞癌的免疫治疗与肝移植:当前及未来挑战
World J Transplant. 2025 Jun 18;15(2):98509. doi: 10.5500/wjt.v15.i2.98509.
2
Precision oncolytic viral therapy in colorectal cancer: Genetic targeting and immune modulation for personalized treatment (Review).结直肠癌的精准溶瘤病毒疗法:用于个性化治疗的基因靶向和免疫调节(综述)
Int J Mol Med. 2025 Jul;56(1). doi: 10.3892/ijmm.2025.5545. Epub 2025 May 9.
3
Immune Cell Engagers: Advancing Precision Immunotherapy for Cancer Treatment.

本文引用的文献

1
Trispecific antibodies enhance the therapeutic efficacy of tumor-directed T cells through T cell receptor co-stimulation.三特异性抗体通过T细胞受体共刺激增强肿瘤定向T细胞的治疗效果。
Nat Cancer. 2020 Jan;1(1):86-98. doi: 10.1038/s43018-019-0004-z. Epub 2019 Nov 18.
2
T-cell receptor mimic (TCRm) antibody therapeutics against intracellular proteins.针对细胞内蛋白的T细胞受体模拟(TCRm)抗体疗法。
Antib Ther. 2019 Jan 21;2(1):22-32. doi: 10.1093/abt/tbz001. eCollection 2019 Jan.
3
The future of cancer immunotherapy: microenvironment-targeting combinations.
免疫细胞衔接器:推动癌症治疗的精准免疫疗法
Antibodies (Basel). 2025 Feb 11;14(1):16. doi: 10.3390/antib14010016.
4
Oncolytic Viruses and Immunotherapy for the Treatment of Uveal Melanoma and Retinoblastoma: The Current Landscape and Novel Advances.溶瘤病毒与免疫疗法治疗葡萄膜黑色素瘤和视网膜母细胞瘤:现状与新进展
Biomedicines. 2025 Jan 6;13(1):108. doi: 10.3390/biomedicines13010108.
5
The implications of oncolytic viruses targeting fibroblasts in enhancing the antitumoural immune response.溶瘤病毒靶向成纤维细胞对增强抗肿瘤免疫反应的影响。
Heliyon. 2024 Oct 10;10(20):e39204. doi: 10.1016/j.heliyon.2024.e39204. eCollection 2024 Oct 30.
6
AVL-armed oncolytic vaccinia virus promotes viral replication and boosts antitumor immunity via increasing ROS levels in pancreatic cancer.携带AVL的溶瘤痘苗病毒通过提高胰腺癌中的活性氧水平促进病毒复制并增强抗肿瘤免疫力。
Mol Ther Oncol. 2024 Sep 17;32(4):200878. doi: 10.1016/j.omton.2024.200878. eCollection 2024 Dec 19.
7
The investigation of oncolytic viruses in the field of cancer therapy.溶瘤病毒在癌症治疗领域的研究。
Front Oncol. 2024 Jul 10;14:1423143. doi: 10.3389/fonc.2024.1423143. eCollection 2024.
8
Overcoming effector T cell exhaustion in ovarian cancer ascites with a novel adenovirus encoding for a MUC1 bispecific antibody engager and IL-2 cytokine.用一种新型腺病毒编码的 MUC1 双特异性抗体结合物和 IL-2 细胞因子克服卵巢癌腹水的效应 T 细胞耗竭。
Mol Ther. 2024 Sep 4;32(9):3114-3127. doi: 10.1016/j.ymthe.2024.06.029. Epub 2024 Jun 22.
9
OV Modulators of the Paediatric Brain TIME: Current Status, Combination Strategies, Limitations and Future Directions.儿科大脑中的 OV 调节剂:当前状态、联合策略、局限性和未来方向。
Int J Mol Sci. 2024 May 3;25(9):5007. doi: 10.3390/ijms25095007.
10
T-Cell Engagers-The Structure and Functional Principle and Application in Hematological Malignancies.T细胞衔接器——结构、功能原理及在血液系统恶性肿瘤中的应用
Cancers (Basel). 2024 Apr 20;16(8):1580. doi: 10.3390/cancers16081580.
癌症免疫疗法的未来:靶向微环境的联合疗法。
Cell Res. 2020 Jun;30(6):507-519. doi: 10.1038/s41422-020-0337-2. Epub 2020 May 28.
4
Fine-tuning bispecific therapeutics.双特异性治疗药物的优化调整。
Pharmacol Ther. 2020 Aug;212:107582. doi: 10.1016/j.pharmthera.2020.107582. Epub 2020 May 23.
5
Therapeutic Cancer Vaccination with an Oncolytic Virus Expressing Membrane-Tethered IL-2.使用表达膜锚定白细胞介素-2的溶瘤病毒进行治疗性癌症疫苗接种。
Mol Ther Oncolytics. 2020 Apr 21;17:350-360. doi: 10.1016/j.omto.2020.04.006. eCollection 2020 Jun 26.
6
Perspective: Designing T-Cell Engagers With Better Therapeutic Windows.观点:设计具有更佳治疗窗口的T细胞衔接器
Front Oncol. 2020 Apr 15;10:446. doi: 10.3389/fonc.2020.00446. eCollection 2020.
7
Challenges and strategies for next-generation bispecific antibody-based antitumor therapeutics.下一代基于双特异性抗体的抗肿瘤治疗药物面临的挑战与策略
Cell Mol Immunol. 2020 May;17(5):451-461. doi: 10.1038/s41423-020-0417-8. Epub 2020 Apr 20.
8
T cell-engaging therapies - BiTEs and beyond.T 细胞结合疗法——双特异性抗体和其他疗法。
Nat Rev Clin Oncol. 2020 Jul;17(7):418-434. doi: 10.1038/s41571-020-0347-5. Epub 2020 Apr 2.
9
New Insights into Mechanisms of Long-term Protective Anti-tumor Immunity Induced by Cancer Vaccines Modified by Virus Infection.病毒感染修饰的癌症疫苗诱导长期保护性抗肿瘤免疫机制的新见解
Biomedicines. 2020 Mar 6;8(3):55. doi: 10.3390/biomedicines8030055.
10
Oncolytic Adenovirus Armed with BiTE, Cytokine, and Checkpoint Inhibitor Enables CAR T Cells to Control the Growth of Heterogeneous Tumors.溶瘤腺病毒武装双特异性 T 细胞结合分子、细胞因子和检查点抑制剂使 CAR T 细胞能够控制异质性肿瘤的生长。
Mol Ther. 2020 May 6;28(5):1251-1262. doi: 10.1016/j.ymthe.2020.02.016. Epub 2020 Feb 24.