Using genetically modified replication-competent (i.e., oncolytic) adenovirus vectors to infect cancer cells and destroy them while having acceptable toxicity in normal tissue is a potential approach to treating cancer. Most studies in this field have investigated the efficiency of these vectors in immunodeficient mice bearing human tumor xenografts. However, this model doesn't fully address the situation in human cancer patients being treated with oncolytic adenovirus because the mouse is immunodeficient as well as non-permissive or semi-permissive for replication of human adenoviruses.
Researchers at Saint Louis University have developed a Syrian hamster model to enable the evaluation of the safety and efficacy of oncolytic adenovirus vectors for treating cancers and other diseases.
The potential advantages of this technology over existing solutions include:
Potential applications of this technology include:
Saint Louis University offers non-exclusive licenses for this technology.