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.
机构:Hammersmith Hosp, Imperial Coll Sch Med, Mol Oncol Unit, Imperial Canc Res Fund, London W12 0NN, England
Heise, C
Kirn, DH
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Hammersmith Hosp, Imperial Coll Sch Med, Mol Oncol Unit, Imperial Canc Res Fund, London W12 0NN, EnglandHammersmith Hosp, Imperial Coll Sch Med, Mol Oncol Unit, Imperial Canc Res Fund, London W12 0NN, England