Department of Radiology and Diagnostic Imaging, Faculty of Medicine, University of Alberta, Edmonton, T6G-2B7, Alberta, Canada.
Curr Drug Deliv. 2011 May;8(3):274-81. doi: 10.2174/156720111795256219.
The interaction of dendritic cells (DCs) and T cells has been the cornerstone of approaches to cancer immunotherapy. Antitumoral immune responses can be elicited by delivering cancer antigens to DCs. As antigen presenting cells, these DCs activate cancer antigen specific T cells. Whereas the first part of the review discusses methods for delivery of cancer vaccines to DCs, in this part the focus is on the potential role of nanoscopic devices for molecular imaging of these immune responses. Nanoscopic devices could potentially deliver tracking molecules to DCs, enabling monitoring of DCs and/or T cell activation and tumoricidal activity during immunotherapy, using non-invasive imaging modalities such as nuclear imaging (single photon emission computed tomography (SPECT), positron emission tomography (PET)), magnetic resonance imaging (MRI) and optical imaging.
树突状细胞 (DCs) 和 T 细胞的相互作用一直是癌症免疫治疗方法的基石。通过将癌症抗原递送至 DCs,可以引发抗肿瘤免疫反应。作为抗原呈递细胞,这些 DCs 激活癌症抗原特异性 T 细胞。虽然综述的第一部分讨论了向 DCs 递送癌症疫苗的方法,但这一部分的重点是纳米设备在这些免疫反应的分子成像中的潜在作用。纳米设备有可能将示踪分子递送至 DCs,从而使用非侵入性成像方式(如核成像(单光子发射计算机断层扫描 (SPECT)、正电子发射断层扫描 (PET))、磁共振成像 (MRI) 和光学成像),在免疫治疗期间监测 DCs 和/或 T 细胞的激活和细胞毒性活性。