4.7 Review

Human Cardiac Gene Therapy

Journal

CIRCULATION RESEARCH
Volume 123, Issue 5, Pages 601-613

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCRESAHA.118.311587

Keywords

AAV; Clinical trial; gene therapy; heart failure; Leber congenital amaurosis; myocardium

Funding

  1. AHA-SDG [17SDG33410873]
  2. NIH [R01 HL139963, R01 HL119046, R01 HL117505, R01 HL128099, R01 HL129814, R01HL131404, T32 HL007824]
  3. Transatlantic Leducq Foundation

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In the past 10 years, there has been tremendous progress made in the field of gene therapy. Effective treatments of Leber congenital amaurosis, hemophilia, and spinal muscular atrophy have been largely based on the efficiency and safety of adeno-associated vectors. Myocardial gene therapy has been tested in patients with heart failure using adeno-associated vectors with no safety concerns but lacking clinical improvements. Cardiac gene therapy is adapting to the new developments in vectors, delivery systems, targets, and clinical end points and is poised for success in the near future.

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