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细胞毒性T细胞作为检测胶质瘤的成像探针。

Cytotoxic T-cells as imaging probes for detecting glioma.

作者信息

Arbab Ali Syed

机构信息

Ali Syed Arbab, Cellular and Molecular Imaging Laboratory, Department of Radiology, Henry Ford Hospital, Detroit, MI 48202, United States.

出版信息

World J Clin Oncol. 2010 Nov 10;1(1):3-11. doi: 10.5306/wjco.v1.i1.3.

Abstract

Tumor vaccination using tumor-associated antigen-primed dendritic cells (DCs) is in clinical trials. Investigators are using patients' own immune systems to activate T-cells against recurrent or metastatic tumors. Following vaccination of DCs or attenuated tumor cells, clinical as well as radiological improvements have been noted due to migration and accumulation of cytotoxic T-cells (CTLs). CTLs mediated tumor cell killing resulted in extended survival in clinical trails and in preclinical models. Besides administration of primed DCs or attenuated or killed tumors cells to initiate the generation of CTLs, investigators have started making genetically altered T-cells (CTLs) to target specific tumors and showed in vivo migration and accumulation in the implanted or recurrent tumors using different imaging modalities. Our groups have also showed the utilization of both in vivo and in vitro techniques to make CTLs against glioma and used them as imaging probes to determine the sites of tumors. In this short review, the current status of vaccination therapy against glioma and utilization of CTLs as in vivo imaging probes to determine the sites of tumors and differentiate recurrent glioma from radiation necrosis will be discussed.

摘要

使用肿瘤相关抗原致敏树突状细胞(DCs)进行肿瘤疫苗接种正处于临床试验阶段。研究人员正在利用患者自身的免疫系统激活T细胞以对抗复发性或转移性肿瘤。在接种DCs或减毒肿瘤细胞后,由于细胞毒性T细胞(CTLs)的迁移和聚集,已观察到临床以及影像学上的改善。CTL介导的肿瘤细胞杀伤导致临床试验和临床前模型中的生存期延长。除了给予致敏DCs或减毒或灭活的肿瘤细胞以启动CTL的生成外,研究人员已开始制造基因改造的T细胞(CTLs)以靶向特定肿瘤,并使用不同的成像方式在植入或复发性肿瘤中显示出体内迁移和聚集。我们的团队还展示了利用体内和体外技术制造针对胶质瘤的CTL,并将其用作成像探针以确定肿瘤部位。在这篇简短的综述中,将讨论针对胶质瘤的疫苗治疗现状以及利用CTL作为体内成像探针来确定肿瘤部位并区分复发性胶质瘤与放射性坏死的情况。

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