Literature DB >> 12700116

Retroviral packaging cells encapsulated in TheraCyte immunoisolation devices enable long-term in vivo gene delivery.

Anna Krupetsky1, Zahida Parveen, Elena Marusich, Adrienne Goodrich, Ralph Dornburg.   

Abstract

The method of delivering a therapeutic gene into a patient is still one of the major obstacles towards successful human gene therapy. Here we describe a novel gene delivery approach using TheraCyte immunoisolation devices. Retroviral vector producing cells, derived from the avian retrovirus spleen necrosis virus, SNV, were encapsulated in TheraCyte devices and tested for the release of retroviral vectors. In vitro experiments show that such devices release infectious retroviral vectors into the tissue culture medium for up to 4 months. When such devices were implanted subcutaneously in SCID mice, infectious virus was released into the blood stream. There, the vectors were transported to and infected tumors, which had been induced by subcutaneous injection of tissue culture cells. Thus, this novel concept of a continuous, long-term gene delivery may constitute an attractive approach for future in vivo human gene therapy.

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Year:  2003        PMID: 12700116     DOI: 10.2741/951

Source DB:  PubMed          Journal:  Front Biosci        ISSN: 1093-4715


  1 in total

1.  Mouse mammary tumor virus promoter-containing retroviral promoter conversion vectors for gene-directed enzyme prodrug therapy are functional in vitro and in vivo.

Authors:  Reinhard Klein; Bärbel Ruttkowski; Sonja Schwab; Thomas Peterbauer; Brian Salmons; Walter H Günzburg; Christine Hohenadl
Journal:  J Biomed Biotechnol       Date:  2008
  1 in total

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