Koido Shigeo, Homma Sadamu, Hara Eiichi, Namiki Yoshihisa, Takahara Akitaka, Komita Hideo, Nagasaki Eijiro, Ito Masaki, Ohkusa Toshifumi, Gong Jianlin, Tajiri Hisao
Division of Gastroenterology and Hepatology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.
Clin Dev Immunol. 2010;2010:516768. doi: 10.1155/2010/516768. Epub 2010 Oct 26.
The goal of cancer vaccines is to induce antitumor immunity that ultimately will reduce tumor burden in tumor environment. Several strategies involving dendritic cells- (DCs)- based vaccine incorporating different tumor-associated antigens to induce antitumor immune responses against tumors have been tested in clinical trials worldwide. Although DCs-based vaccine such as fusions of whole tumor cells and DCs has been proven to be clinically safe and is efficient to enhance antitumor immune responses for inducing effective immune response and for breaking T-cell tolerance to tumor-associated antigens (TAAs), only a limited success has occurred in clinical trials. This paper reviews tumor immune escape and current strategies employed in the field of tumor/DC fusions vaccine aimed at enhancing activation of TAAs-specific cytotoxic T cells in tumor microenvironment.
癌症疫苗的目标是诱导抗肿瘤免疫,最终减轻肿瘤环境中的肿瘤负担。全世界的临床试验已经测试了几种基于树突状细胞(DCs)的疫苗策略,这些策略整合了不同的肿瘤相关抗原,以诱导针对肿瘤的抗肿瘤免疫反应。尽管基于DCs的疫苗,如全肿瘤细胞与DCs的融合物,已被证明在临床上是安全的,并且在增强抗肿瘤免疫反应以诱导有效免疫反应和打破T细胞对肿瘤相关抗原(TAA)的耐受性方面是有效的,但在临床试验中仅取得了有限的成功。本文综述了肿瘤免疫逃逸以及肿瘤/DC融合疫苗领域为增强肿瘤微环境中TAA特异性细胞毒性T细胞的激活而采用的当前策略。