Viral vectors for cancer immunotherapy

被引:23
作者
Harrop, R
Carroll, MW
机构
[1] Oxford BioMed Uk Ltd, Oxford OX4 4GA, England
[2] Univ Reading, Ctr Sci & Technol, MNLpharma Ltd, Reading RG6 6AH, Berks, England
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2006年 / 11卷
关键词
cancer; tumor; neoplasia; immunotherapy; vaccine; tumor antigen; viral vectors; review;
D O I
10.2741/1838
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Over the last decade, immunotherapy approaches for the treatment of cancer have been investigated with renewed vigour, perhaps catalyzed by the clinical successes seen with monoclonal antibody and cytokine based therapies. The identification of tumor-associated antigens (TAAs) in multiple cancer types has enabled the development of targeted immunotherapies and allayed some of the safety concerns associated with the induction of deleterious autoimmune reactions. In addition to the TAA or therapeutic gene, the antigen delivery system is equally as important for the development of a successful cancer vaccine. One approach to induce a potent and targeted antitumor response is to use viruses to deliver the TAA to cells of the immune system. A diverse array of oncolytic viruses and recombinant viral vectors encoding numerous therapeutic genes or TAAs have been tested in pre-clinical studies and produced results which, in some cases, justify their clinical development as potential cancer immunotherapies. Within the last 5-10 years, many such recombinant vectors have made the transition from preclinical research to clinical development and it is these, which are given most weight in this review.
引用
收藏
页码:804 / 817
页数:14
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