Wang Bin, Sun Chong, Wang Sijia, Shang Na, Figini Matteo, Ma Quanhong, Gu Shanzhi, Procissi Daniele, Yaghmai Vahid, Li Guoxin, Larson Andrew, Zhang Zhuoli
Department of General Surgery, Nanfang Hospital, Southern Medical University, Guangdong Provincial Engineering Technology Research Center of Minimally Invasive SurgeryGuangzhou, China.
Department of Radiology, Feinberg School of Medicine, Northwestern UniversityChicago, IL, USA.
Am J Transl Res. 2017 Oct 15;9(10):4564-4573. eCollection 2017.
In recent decades, immunotherapy has undergone extensive developments for oncologic therapy applications. Dendritic cells (DCs) plays a fundamental role in cell-based vaccination immunotherapy against various types of cancer. It involves stimulating innate and adaptive immunity, in particular cytotoxic T-cell mediated antitumor effects, against targeted tumors and has been studied in both preclinical and clinical settings. Nevertheless, clinical outcomes have been unsatisfying. The antitumor response requires sufficient migration of viable DCs from primary administration site to targeted tumors through related lymphatics. The dynamics and mechanisms of the DCs migration still need further investigation. Here, we briefly introduce the current clinically applicable methods for manufacturing DC-based cancer vaccines and their most commonly used non-invasive, real-time tracking approaches. Furthermore, we propose a hypothesis that intraperitoneal injection may improve the efficiency of DC-based cancer vaccine.
近几十年来,免疫疗法在肿瘤治疗应用方面取得了广泛进展。树突状细胞(DCs)在针对各类癌症的基于细胞的疫苗接种免疫疗法中发挥着基础性作用。它涉及激发先天性和适应性免疫,特别是细胞毒性T细胞介导的针对靶向肿瘤的抗肿瘤效应,并且已在临床前和临床环境中进行了研究。然而,临床结果并不令人满意。抗肿瘤反应需要有活力的DCs从初次给药部位通过相关淋巴管充分迁移至靶向肿瘤。DCs迁移的动态过程和机制仍需进一步研究。在此,我们简要介绍目前临床上用于制备基于DC的癌症疫苗的适用方法及其最常用的非侵入性实时追踪方法。此外,我们提出一个假说,即腹腔注射可能会提高基于DC的癌症疫苗的效率。