Abstract

Strategies to alter the tropism of adenovirus provide the means to enhance vector potency and to allow cell-specific targeting. One approach to this end involves genetic capsid modification. Specifically, incorporation of targeting ligands within the capsid structure can allow substantial alterations in tropism. Various capsid sites have been studied as locales for incorporation of heterologous targeting ligands. At present, the ideal site for incorporation of such ligands with fidelity preservation has not been identified. None-the-less, efforts to date have allowed significant gain in terms of the goals of vector potency enhancement and cell specific targeting.

Original languageEnglish
Title of host publicationVector Targeting for Therapeutic Gene Delivery
Publisherwiley
Pages171-200
Number of pages30
ISBN (Electronic)9780471234302
ISBN (Print)9780471434795
DOIs
StatePublished - Jan 1 2003

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