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Published on: June 2, 2019
Gene-based therapies in patients with critical limb ischemia
Panagiotis Kitrou1, Dimitris Karnabatidis1, Elias Brountzos2
1a Department of Interventional Radiology , Patras University Hospital , Rio , Greece.
Insights
Growth factor gene therapy for critical limb ischemia (CLI) shows potential for treating
Area of Science:
- Vascular Biology and Regenerative Medicine
- Gene Therapy
- Ischemic Disease Treatment
Background:
- Critical limb ischemia (CLI) is a severe condition with limited treatment options.
- Revascularization is the primary treatment, but many patients are ineligible.
- Gene therapy using growth factors for angiogenesis is being explored for 'no-option' CLI patients.
Purpose of the Study:
- To review current growth factor-based gene therapies for CLI.
- To discuss challenges and future perspectives in therapeutic angiogenesis for CLI.
- To contextualize gene therapy within personalized treatment strategies for CLI.
Main Methods:
- Literature review of studies on growth factor gene delivery for CLI.
- Analysis of outcomes, challenges, and emerging technologies.
- Discussion of therapeutic angiogenesis in the framework of tailored CLI therapy.
Main Results:
- Growth factor therapy for CLI has yielded equivocal and inconclusive results.
- Gene therapy's potential lies in activating angiogenesis and arteriogenesis at the micro-circulatory level.
- Personalized treatment approaches are crucial for managing CLI.
Conclusions:
- Growth factor gene therapy is not a panacea for CLI but can be an adjunct in personalized treatment.
- Further research and technological advancements are needed to optimize therapeutic angiogenesis.
- Tailored therapeutic strategies are essential for improving outcomes in CLI patients.
Introduction:
Critical limb ischemia (CLI) constitutes a life-limiting and life-threatening disease. Revascularization, either endovascular or surgical, remains the best treatment option accompanied by medication and risk factor modification. Patients unable to undergo revascularization, referred as 'no-option patients', have been the center of interest the last few years, subjected to treatment therapies based on proteins (mainly growth factors) involved in angiogenesis via gene delivery to the ischemic tissue. Areas covered: This review focuses on these growth factors, gives an update of the studies available, discusses the possible problems that influence outcomes and describes future perspectives including possible new technologies that will improve them. Additionally, the authors attempt to place therapeutic angiogenesis to the bigger frame of tailored therapy in CLI. Expert opinion: Although encouraging in the beginning, growth factor therapy results have been equivocal and inconclusive. And while it would be misleading to approach gene therapy as panacea, its effect on the micro-circulatory level activating angiogenesis and arteriogenesis could act as an important adjunct in personalized treatment.
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