Design of Improved Oncolytic Adenoviruses

被引:21
|
作者
Alemany, Ramon [1 ]
机构
[1] Inst Catala Oncol IDIBELL, Translat Res Lab, Barcelona, Spain
关键词
POTENT ANTITUMOR EFFICACY; T-CELL RESPONSES; INTRATUMORAL SPREAD; BINDING ABLATION; CANCER; VECTOR; EXPRESSION; DELIVERY; REPLICATION; CARRIERS;
D O I
10.1016/B978-0-12-398342-8.00004-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
During the last decade adenovirus has lost its appeal in gene therapy due to a high immunogenicity that leads to a transient gene expression. However, adenovirus has gained attention as replication-competent vector to treat cancer. Designed for virotherapy, adenovirus has been successfully modified to replicate selectively in tumor cells. After the initial clinical trials with tumor-selective adenoviruses, it has become clear that further improvements on tumor targeting, intratumoral dissemination, and modulation of antiviral and antitumor immune responses are needed to effectively treat cancer. The non-viral delivery of infectious DNA encoding an oncolytic adenovirus armed with extracellular matrix-degrading genes and with genes that regulate the immune system to favor antitumor instead of antiviral immunity are key in the design oncolytic adenovirus.
引用
收藏
页码:93 / 114
页数:22
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