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Right arrow Transplantation - heart

Eur J Cardiothorac Surg 2001;19:702-707
© 2001 Elsevier Science NL

Conditions of vector delivery improve efficiency of adenoviral-mediated gene transfer to the transplanted heart

John Yapa, Carlo Pellegrinia, Timothy O'Brienb, Henry D. Tazelaarc, Christopher G.A. McGregora

a Department of Surgery, Mayo Clinic and Foundation, Rochester, MN 55905, USA
b Division of Endocrinology and Metabolism, Mayo Clinic and Foundation, Rochester, MN 55905, USA
c Department of Laboratory Medicine and Pathology, Mayo Clinic and Foundation, Rochester, MN 55905, USA

Received 18 August 2000; received in revised form 12 February 2001; accepted 9 March 2001.

Corresponding author. Tel.: +1-507-255-6038; fax: +1-507-255-4500
e-mail: mcgregor.christopher{at}mayo.edu

Objectives: Conditions for ex vivo gene transfer to the transplanted heart were studied in a model of syngeneic abdominal heterotopic heart transplantation in the rat. Various methods of adenoviral-mediated gene transfer to the transplanted heart were compared. Methods: In the first experiment, a dose response study, an adenoviral vector encoding the ß-galactosidase gene was infused into the donor heart with the pulmonary artery open and flushed out prior to performing the transplant. In the second experiment, the effects of clamping the pulmonary artery during vector infusion and not flushing out the viral solution, resulting in vector dwell during the warm ischemia, were examined. Results: In the first experiment, gene transfer was relatively inefficient; however, transgene expression improved with increases in the vector dose (range, 1x107–1x109). The efficiency of gene transfer was significantly greater when the conditions of the second experiment were applied. In all models studied, cardiomyocytes and not vascular endothelial cells were the predominant cell type transduced. Conclusions: This study indicates that the conditions of adenoviral vector delivery are critical for optimizing gene transfer in the transplant setting. In addition, intravascular administration of adenoviral vector to the donor heart results predominantly in cardiomyocyte transgene expression.

Key Words: Adenovirus • Gene therapy • Gene transfer • Heart • Transplantation




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Eur. J. Cardiothorac. Surg.Home page
D. Ricci, A. A. Mennander, L. D. Pham, V. P. Rao, N. Miyagi, G. W. Byrne, S. J. Russell, and C. G.A. McGregor
Non-invasive radioiodine imaging for accurate quantitation of NIS reporter gene expression in transplanted hearts
Eur. J. Cardiothorac. Surg., January 1, 2008; 33(1): 32 - 39.
[Abstract] [Full Text] [PDF]




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Copyright © 2001 European Association for Cardio-Thoracic Surgery. Published by Elsevier. All rights reserved.