• 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

抗原受体基因修饰的 T 细胞治疗脑胶质瘤。

Antigen-receptor gene-modified T cells for treatment of glioma.

机构信息

Department of Immuno-Gene Therapy, Mie University Graduate School of Medicine, Tsu, Japan.

出版信息

Adv Exp Med Biol. 2012;746:202-15. doi: 10.1007/978-1-4614-3146-6_16.

DOI:10.1007/978-1-4614-3146-6_16
PMID:22639170
Abstract

Immunological effector cells and molecules have been shown to access intracranial tumor sites despite the existence of blood brain barrier (BBB) or immunosuppressive mechanisms associated with brain tumors. Recent progress in T-cell biology and tumor immunology made possible to develop strategies of tumor-associated antigen-specific immunotherapeutic approaches such as vaccination with defined antigens and adoptive T-cell therapy with antigen-specific T cells including gene-modified T cells for the treatment of patients with brain tumors. An array of recent reports on the trials of active and passive immunotherapy for patients with brain tumors have documented safety and some preliminary clinical efficacy, although the ultimate judgment for clinical benefits awaits rigorous evaluation in trials of later phases. Nevertheless, treatment with lymphocytes that are engineered to express tumor-specific receptor genes is a promising immunotherapy against glioma, based on the significant efficacy reported in the trials for patients with other types of malignancy. Overcoming the relative difficulty to apply immunotherapeutic approach to intracranial region, current advances in the understanding of human tumor immunology and the gene-therapy methodology will address the development of effective immunotherapy of brain tumors.

摘要

免疫效应细胞和分子已被证明可以进入颅内肿瘤部位,尽管存在血脑屏障 (BBB) 或与脑肿瘤相关的免疫抑制机制。T 细胞生物学和肿瘤免疫学的最新进展使得开发肿瘤相关抗原特异性免疫治疗策略成为可能,例如用定义的抗原进行疫苗接种,以及用抗原特异性 T 细胞进行过继性 T 细胞治疗,包括基因修饰的 T 细胞,用于治疗脑肿瘤患者。最近有大量关于脑肿瘤患者主动和被动免疫治疗试验的报告,记录了安全性和一些初步的临床疗效,尽管最终的临床获益判断仍有待更严格的后期试验评估。然而,基于对其他类型恶性肿瘤患者试验中报告的显著疗效,用表达肿瘤特异性受体基因的淋巴细胞进行治疗是一种有前途的治疗胶质母细胞瘤的免疫疗法。为了克服将免疫治疗方法应用于颅内区域的相对困难,目前对人类肿瘤免疫学和基因治疗方法的理解的进展将解决脑肿瘤有效免疫治疗的发展问题。

相似文献

1
Antigen-receptor gene-modified T cells for treatment of glioma.抗原受体基因修饰的 T 细胞治疗脑胶质瘤。
Adv Exp Med Biol. 2012;746:202-15. doi: 10.1007/978-1-4614-3146-6_16.
2
Genetically Engineered T-Cells for Malignant Glioma: Overcoming the Barriers to Effective Immunotherapy.基因工程 T 细胞治疗恶性脑胶质瘤:克服免疫治疗的障碍。
Front Immunol. 2019 Jan 22;9:3062. doi: 10.3389/fimmu.2018.03062. eCollection 2018.
3
Cellular immunotherapy for malignant gliomas.恶性脑胶质瘤的细胞免疫治疗。
Expert Opin Biol Ther. 2016 Oct;16(10):1265-75. doi: 10.1080/14712598.2016.1214266. Epub 2016 Jul 29.
4
Cytokine therapy.细胞因子治疗。
Adv Exp Med Biol. 2012;746:86-94. doi: 10.1007/978-1-4614-3146-6_7.
5
Genetically Modified Cellular Therapies for Malignant Gliomas.用于恶性脑胶质瘤的基因修饰细胞治疗。
Int J Mol Sci. 2021 Nov 26;22(23):12810. doi: 10.3390/ijms222312810.
6
Dendritic cell vaccines.树突状细胞疫苗。
Adv Exp Med Biol. 2012;746:187-200. doi: 10.1007/978-1-4614-3146-6_15.
7
Basic concepts in glioma immunology.神经胶质瘤免疫学基础概念。
Adv Exp Med Biol. 2012;746:42-52. doi: 10.1007/978-1-4614-3146-6_4.
8
T-cell immunotherapy for malignant glioma: toward a combined approach.T 细胞免疫疗法治疗恶性脑胶质瘤:联合治疗方法的探索。
Curr Opin Oncol. 2010 Nov;22(6):604-10. doi: 10.1097/CCO.0b013e32833dead8.
9
Pre-Clinical Models for CAR T-Cell Therapy for Glioma.用于脑胶质瘤嵌合抗原受体 T 细胞治疗的临床前模型。
Cells. 2024 Sep 4;13(17):1480. doi: 10.3390/cells13171480.
10
[Cellular immunotherapy for malignant glioma].[恶性胶质瘤的细胞免疫治疗]
Nihon Rinsho. 2005 Sep;63 Suppl 9:557-62.

引用本文的文献

1
miR-526b-3p serves as a prognostic factor and regulates the proliferation, invasion, and migration of glioma through targeting WEE1.微小RNA-526b-3p作为一种预后因素,通过靶向WEE1来调节神经胶质瘤的增殖、侵袭和迁移。
Cancer Manag Res. 2019 Apr 11;11:3099-3110. doi: 10.2147/CMAR.S192361. eCollection 2019.
2
Advances in Immunotherapy for Glioblastoma Multiforme.胶质母细胞瘤的免疫治疗进展。
J Immunol Res. 2017;2017:3597613. doi: 10.1155/2017/3597613. Epub 2017 Feb 19.
3
Recent advances and future of immunotherapy for glioblastoma.
胶质母细胞瘤免疫治疗的最新进展和未来。
Expert Opin Biol Ther. 2016 Oct;16(10):1245-64. doi: 10.1080/14712598.2016.1212012. Epub 2016 Jul 27.
4
Overview of current immunotherapeutic strategies for glioma.胶质瘤当前免疫治疗策略概述
Immunotherapy. 2015;7(10):1073-104. doi: 10.2217/imt.15.75.
5
Experiences and expectations for glioma immunotherapeutic approaches.胶质瘤免疫治疗方法的经验与期望。
Front Oncol. 2014 Dec 10;4:355. doi: 10.3389/fonc.2014.00355. eCollection 2014.