嵌合抗原受体
碘化钠转运体
正电子发射断层摄影术
体内
癌症研究
临床前影像学
抗原
细胞疗法
T细胞
医学
细胞
化学
生物
核医学
免疫学
共转运蛋白
免疫系统
基因
生物化学
生物技术
运输机
作者
Reona Sakemura,Michelle J. Cox,Aditya Bansal,Claudia Manriquez Roman,Mehrdad Hefazi,Cynthia J. Vernon,Dianna L. Glynn,Mukesh K. Pandey,Timothy R. DeGrado,Elizabeth L. Siegler,Saad S. Kenderian
摘要
T cells genetically engineered to express chimeric antigen receptors (CAR) have shown unprecedented results in pivotal clinical trials for patients with B cell malignancies or multiple myeloma (MM). However, numerous obstacles limit the efficacy and prohibit the widespread use of CAR T cell therapies due to poor trafficking and infiltration into tumor sites as well as lack of persistence in vivo. Moreover, life-threatening toxicities, such as cytokine release syndrome or neurotoxicity, are major concerns. Efficient and sensitive imaging and tracking of CAR T cells enables the evaluation of T cell trafficking, expansion, and in vivo characterization and allows the development of strategies to overcome the current limitations of CAR T cell therapy. This paper describes the methodology for incorporating the sodium iodide symporter (NIS) in CAR T cells and for CAR T cell imaging using [18F]tetrafluoroborate-positron emission tomography ([18F]TFB-PET) in preclinical models. The methods described in this protocol can be applied to other CAR constructs and target genes in addition to the ones used for this study.
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