Genetic Enhancement of Stem Cell Engraftment, Survival, and Efficacy

Author:

Penn Marc S.1,Mangi Abeel A.1

Affiliation:

1. From the Skirball Laboratory for Cardiovascular Cellular Therapeutics (M.S.P.), Center for Cardiovascular Cell Therapy, Heart and Vascular Institute, Departments of Cardiovascular Medicine and Stem Cell Biology and Regenerative Medicine, and the Department of Thoracic and Cardiovascular Surgery (A.A.M.), Cleveland Clinic, Cleveland, Ohio.

Abstract

Cell-based therapies for the prevention and treatment of cardiac dysfunction offer the potential to significantly modulate cardiac function and improve outcomes in patients with cardiovascular disease. To date several clinical studies have suggested the potential efficacy of several different stem cell types; however, the benefits seen in clinical trials have been inconsistent and modest. In parallel, preclinical studies have identified key events in the process of cell-based myocardial repair, including stem cell homing, engraftment, survival, paracrine factor release, and differentiation that need to be optimized to maximize cardiac repair and function. The inconsistent and modest benefits seen in clinical trials combined with the preclinical identification of mediators responsible for key events in cell-based cardiac repair offers the potential for cell-based therapy to advance to cell-based gene therapy in an attempt to optimize these key events in the hope of maximizing clinical benefit. Below we discuss potential key events in cardiac repair and the mediators of these events that could be of potential interest for genetic enhancement of stem cell–based cardiac repair.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

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