© 1997 by European Society of Cardiology
Copyright © 1997, European Society of Cardiology
Prospects for adenovirus-mediated gene therapy of inherited diseases of the myocardium
aDepartment of Pediatrics, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA
bDepartment of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA
* Corresponding author. Pediatric Cardiology, Baylor College of Medicine, One Baylor Plaza, Room 333E, Houston TX 77030, USA. Tel.: +1 713 7987342; Fax: +1 713 7988085; E-mail: jtowbin@bcm.tmc.edu
Received 10 February 1997; accepted 5 June 1997
KEYWORDS Adenovirus; Cardiomyopathy; Long QT
| The first 150 words of the full text of this article appear below. |
| 1 Introduction |
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Many genetic loci linked to a variety of diseases have been identified, and disease-causing mutations characterized. These have included diseases of the myocardium, such as X-linked dilated cardiomyopathy [1–3], hypertrophic cardiomyopathy [4–6], and Long QT syndrome [7–9]. The elucidation of gene defects has allowed different therapeutic strategies to be proposed, including the use of pharmaceutical agents to replace or to antagonize the mutated protein, and replacement of the defective gene with a functional one (gene therapy). There have been many publications describing the use of vectors to transduce target cells for the correction of gene defects or for anti-viral therapy (for reviews see [10–14]). Such vectors have included recombinant retroviruses, adenoviruses, adeno-associated viruses, and herpes viruses, as well as non-viral vectors. Each vector has inherent advantages and disadvantages. At this time the adenoviruses are most commonly used and represent the most likely vector for efficient transduction
| 2 Recombinant adenoviruses as gene therapy vectors |
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| 3 Dilated cardiomyopathy |
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| 4 Hypertrophic cardiomyopathy |
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| 5 Long QT syndrome |
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| 6 Adenovirus-mediated cardiac disease |
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| 7 Summary |
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