Imaging of T-cells and their responses during anti-cancer immunotherapy

被引:77
作者
Krekorian, Massis [1 ,2 ]
Fruhwirth, Gilbert O. [3 ]
Srinivas, Mangala [1 ]
Figdor, Carl G. [1 ]
Heskamp, Sandra [2 ]
Witney, Timothy H. [3 ]
Aarntzen, Erik H. J. G. [2 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Radboud Inst Mol Life Sci, Dept Tumor Immunol, Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Dept Radiol & Nucl Med, Nijmegen, Netherlands
[3] Kings Coll London, Sch Biomed Engn & Imaging Sci, Dept Imaging Chem & Biol, London, England
基金
英国工程与自然科学研究理事会; 欧洲研究理事会; 英国惠康基金;
关键词
Immunotherapy; cell-based therapy; in vivo imaging; T-cells; positron emission tomography; SODIUM-IODIDE SYMPORTER; IN-VIVO TRACKING; TUMOR-INFILTRATING LYMPHOCYTES; REPORTER GENE; SODIUM/IODIDE SYMPORTER; RADIATION-DOSIMETRY; CHEMOKINE RECEPTOR; PET PROBE; PERFORMANCE EVALUATION; DOPAMINE-D-2; RECEPTOR;
D O I
10.7150/thno.37924
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Immunotherapy has proven to be an effective approach in a growing number of cancers. Despite durable clinical responses achieved with antibodies targeting immune checkpoint molecules, many patients do not respond. The common denominator for immunotherapies that have successfully been introduced in the clinic is their potential to induce or enhance infiltration of cytotoxic T-cells into the tumour. However, in clinical research the molecules, cells and processes involved in effective responses during immunotherapy remain largely obscure. Therefore, in vivo imaging technologies that interrogate T-cell responses in patients represent a powerful tool to boost further development of immunotherapy. This review comprises a comprehensive analysis of the in vivo imaging technologies that allow the characterisation of T-cell responses induced by anti-cancer immunotherapy, with emphasis on technologies that are clinically available or have high translational potential. Throughout we discuss their respective strengths and weaknesses, providing arguments for selecting the optimal imaging options for future research and patient management.
引用
收藏
页码:7924 / 7947
页数:24
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