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Updated: May 1, 2026

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In Vivo Gene Transfer to the Rabbit Common Carotid Artery Endothelium
Published on: May 6, 2018
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Cell and gene therapy approaches for cardiac vascularization
Ludovic Melly1, Stefano Boccardo2, Friedrich Eckstein3
1Cell and Gene Therapy, Department of Biomedicine and Department of Surgery, Basel University Hospital, Basel 4031, Switzerland. lmelly@uhbs.ch.
Cells
|April 9, 2014
Summary
Developing safe and effective therapeutic angiogenesis for cardiac ischemia remains challenging. Controlled Vascular Endothelial Growth Factor (VEGF) delivery is crucial for stable vascular growth, avoiding aberrant development.
Area of Science:
- Cardiovascular Research
- Regenerative Medicine
- Molecular Biology
Background:
- Therapeutic angiogenesis shows promise for treating cardiac ischemia, but lacks safe and effective clinical methods.
- Vascular Endothelial Growth Factor (VEGF) is key to blood vessel formation but requires precise control to prevent abnormal growth.
Purpose of the Study:
- To review current limitations and future prospects of VEGF gene therapy for cardiac ischemia.
- To evaluate cell-based strategies for implementing controlled therapeutic angiogenesis in heart disease.
Main Methods:
- Literature review of preclinical and clinical studies on VEGF-based therapies.
- Analysis of gene therapy and cell-based approaches for controlled VEGF delivery.
- Discussion of challenges in achieving sustained, safe, and functional vascularization.
Main Results:
- Current VEGF strategies often fail to achieve controlled, localized, and sustained expression.
- Aberrant vascularization and lack of functional integration are significant hurdles.
- Cell-based delivery offers potential for improved spatial and temporal control of VEGF.
Conclusions:
- Precise control over VEGF levels and distribution is essential for successful therapeutic angiogenesis in cardiac ischemia.
- Further research into refined gene and cell-based delivery systems is needed to overcome current limitations and enable clinical translation.
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