Mossoba Miriam E, Medin Jeffrey A
Department of Medical Biophysics, University of Toronto, 67 College Street, Room 426, Toronto, Ontario, M5G 2MI, Canada.
Expert Rev Vaccines. 2006 Oct;5(5):717-32. doi: 10.1586/14760584.5.5.717.
The immune system uses a process known as 'immunosurveillance' to help prevent the outgrowth of tumors. In cancer immunotherapy, a major goal is for immunity against tumor-associated antigens to be generated or strengthened in patients. To achieve this goal, several approaches have been tested, including the use of highly potent antigen-presenting cells called dendritic cells (DCs), which can activate T cells efficiently. Presentation of peptides derived from tumor antigens on the surface of DCs can stimulate strong antitumor immunity. Using recombinant viral vectors encoding tumor-associated antigens, DCs can be engineered efficiently to express sustained levels of tumor-antigen peptides. This review discusses the effectiveness of virally transduced DCs in treating tumors and generating antigen-specific T-cell responses. It covers mouse and nonhuman primate studies, preclinical in vitro human cell experiments and clinical trials.
免疫系统利用一种称为“免疫监视”的过程来帮助预防肿瘤的生长。在癌症免疫治疗中,一个主要目标是在患者体内产生或增强针对肿瘤相关抗原的免疫力。为了实现这一目标,已经测试了几种方法,包括使用称为树突状细胞(DCs)的高效抗原呈递细胞,其可以有效地激活T细胞。DCs表面呈现源自肿瘤抗原的肽可以刺激强大的抗肿瘤免疫力。使用编码肿瘤相关抗原的重组病毒载体,可以有效地改造DCs以表达持续水平的肿瘤抗原肽。这篇综述讨论了病毒转导的DCs在治疗肿瘤和产生抗原特异性T细胞反应方面的有效性。它涵盖了小鼠和非人类灵长类动物研究、临床前体外人类细胞实验和临床试验。