Literature DB >> 9415288

Prevention of vein graft failure: potential applications for gene therapy.

A H Baker1, D Mehta, S J George, G D Angelini.   

Abstract

The use of gene therapy in the clinical setting is believed to be a realistic option for the future. Many clinical trials are underway for treatment of disorders as diverse as cancer, peripheral vascular disease, and numerous monogenic disease. However, gene therapy for vein graft failure may be more distant due to the highly complex, multifactorial aetiology of the disease. Although many of the cellular mechanisms involved in vein graft failure have been reported, important barriers still need to be overcome before gene therapy could become a clinical reality. Further understanding of the molecular mechanisms involved in graft failure will lead to the identification of appropriate therapeutic genes. Moreover, limitations in the current delivery systems need to be overcome to allow efficient, safe delivery and expression of transgenes for the required length of time in vivo. However, currently available gene delivery vectors are extremely useful tools to help in our understanding of vein graft failure. In this review, we address the issues surrounding gene therapy with particular emphasis on its future potential to ameliorate long term vein graft occlusion.

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Year:  1997        PMID: 9415288     DOI: 10.1016/s0008-6363(97)00116-8

Source DB:  PubMed          Journal:  Cardiovasc Res        ISSN: 0008-6363            Impact factor:   10.787


  4 in total

Review 1.  Gene transfer to the vasculature: historical perspective and implication for future research objectives.

Authors:  Sarah J George; Andrew H Baker
Journal:  Mol Biotechnol       Date:  2002-10       Impact factor: 2.695

Review 2.  Cardiac gene therapy: are we there yet?

Authors:  P N Matkar; H Leong-Poi; K K Singh
Journal:  Gene Ther       Date:  2016-04-29       Impact factor: 5.250

3.  Gene Therapy for Cardiovascular Disease.

Authors:  Kate L. Dishart; Lorraine M. Work; Laura Denby; Andrew H. Baker
Journal:  J Biomed Biotechnol       Date:  2003

4.  Improved gene delivery to human saphenous vein cells and tissue using a peptide-modified adenoviral vector.

Authors:  Lorraine M Work; Paul N Reynolds; Andrew H Baker
Journal:  Genet Vaccines Ther       Date:  2004-10-08
  4 in total

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