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Virus Vectors

Chimeras redirect adenovirus transduction in vitro and in vivo

Published in Gene Therapy Weekly, February 27th, 2003

Researchers at Cornell University have developed chimeras that can redirect adenovirus vectors used in gene therapies.

"Altering adenovirus vector (Ad vector) targeting is an important goal for a variety of gene therapy applications and involves eliminating or reducing the normal tropism of a vector and retargeting through a distinct receptor-ligand pathway. The first step of Ad vector infection is high-affinity binding to a target cellular receptor. For the majority of adenoviruses and Ad vectors, the fiber capsid protein serves this purpose, binding to the coxsackievirus and adenovirus receptor (CAR) present on a variety of cell types," reported researchers at the...

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