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Immobilization of gene vectors on polyurethane surfaces using a monoclonal antibody for localized gene delivery
Author(s) -
Mei Lin,
Jin Xu,
Song Cunxian,
Wang Manyan,
Levy R. J.
Publication year - 2006
Publication title -
the journal of gene medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.689
H-Index - 91
eISSN - 1521-2254
pISSN - 1099-498X
DOI - 10.1002/jgm.912
Subject(s) - gene delivery , viral vector , transduction (biophysics) , monoclonal antibody , green fluorescent protein , genetic enhancement , antibody , microbiology and biotechnology , in vivo , transfection , biology , chemistry , gene , biophysics , immunology , recombinant dna , biochemistry
Abstract Background Conventional strategies of gene therapy using viral vectors result in suboptimal localization and potentially dangerous distal spread of vector. We hypothesized that localized delivery of adenoviral gene vectors could be achieved from a polyurethane (PU) film through a mechanism involving anti‐viral antibody tethering. Methods PU films were formulated with a collagen coating. Anti‐adenoviral monoclonal antibodies were covalently bound to the collagen surface. These antibodies enabled tethering of replication‐defective adenoviruses [Ad‐GFP (encoding green fluorescent protein)] through highly specific antigen‐antibody affinity. The binding stability and in vitro delivery of virus bound on PU films were investigated. Cell culture studies with rat arterial smooth muscle cells (A10) assessed transduction on or near the PU matrix. In vivo experiments with collagen‐coated PU films investigated atrial epicardial implant and subdermal implant models in Yorkshire swine. Results We report for the first time successful PU film‐based gene delivery using antibody‐tethered adenovirus encoding the green fluorescent protein (GFP), demonstrating efficient and highly localized gene delivery to arterial smooth muscle cells in cell culture and pig implant. In comparison, direct injections of viral vectors into subcutaneous sites gave sparse, needle‐track‐oriented GFP expression patterns. Conclusion We conclude that PU film is a suitable platform for a localizable viral vector delivery system that also prevents systemic spread of vector. Gene delivery using PU film‐based anti‐viral antibody tethering of vectors should be suitable for a wide array of single or multiple therapeutic gene strategies, and for further device‐based gene delivery therapeutic strategies. Copyright © 2006 John Wiley & Sons, Ltd.