Cancer immunotherapy using virally transduced dendritic cells: animal studies and human clinical trials

被引:39
作者
Mossoba, Miriam E.
Medin, Jeffrey A.
机构
[1] Univ Hlth Network, Ontario Canc Inst, Toronto, ON M5G 2M1, Canada
[2] Univ Toronto, Dept Med Biophys, Toronto, ON M5G 2M1, Canada
[3] Univ Toronto, Inst Med Sci, Toronto, ON M5G 2M1, Canada
关键词
adeno-assosiated virus; adenovirus; canarypox virus; cancer; clinical trials; dendritic cells; fowlpox virus; immunotherapy; lentivirus; onco-retrovirus; vaccinia virus;
D O I
10.1586/14760584.5.5.717
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
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.
引用
收藏
页码:717 / 732
页数:16
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