Gene therapy approaches for cardiovascular diseases

Rozenn Quarck1, Paul Holvoet

  • 1Cardiovascular Research Unit, Center for Experimental Surgery and Anesthesiology, Katholieke Universiteit Leuven, Belgium.

Insights

Gene therapy offers a promising new treatment for cardiovascular diseases, with ongoing human trials exploring various delivery methods and vectors. New strategies combine gene therapy with cell therapy and tissue engineering for enhanced vascular and cardiac repair.

Area of Science:

  • Cardiovascular research
  • Gene therapy applications
  • Regenerative medicine

Background:

  • Cardiovascular diseases (CVDs) are a leading cause of mortality in Western nations.
  • Gene therapy is an emerging treatment strategy for various CVDs, including peripheral arterial disease and ischemic heart disease.
  • Significant advancements in gene transfer have led to ongoing human clinical trials.

Purpose of the Study:

  • To provide an overview of gene transfer strategies for cardiovascular diseases.
  • To highlight current delivery routes and vectors used in animal studies and clinical trials.
  • To focus on novel approaches like combined gene and cell therapy, gene silencing, and targeted gene delivery.

Main Methods:

  • Review of existing gene transfer strategies.
  • Analysis of delivery routes and vectors in preclinical and clinical studies.
  • Exploration of emerging techniques such as gene silencing and targeted gene delivery.

Main Results:

  • Gene therapy has shown remarkable progress over the past decade.
  • Various delivery routes and vectors are being utilized in animal models and human trials.
  • New approaches are being developed for gene targeting to the vascular wall and myocardium.

Conclusions:

  • Gene therapy holds significant potential for treating cardiovascular diseases.
  • Combination therapies involving gene therapy, cell therapy, and tissue engineering are promising.
  • Advanced techniques for gene silencing and targeted delivery represent the future of cardiovascular gene therapy.

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