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Intravenous infusions of mesenchymal stromal cells have cumulative beneficial effects in a porcine model of chronic ischemic cardiomyopathy.
Tang, Xian-Liang; Wysoczynski, Marcin; Gumpert, Anna M; Solanki, Mitesh; Li, Yan; Wu, Wen-Jian; Zheng, Shirong; Ruble, Halina; Li, Hong; Stowers, Heather; Zheng, Shengnan; Ou, Qinghui; Tanveer, Nida; Slezak, Jan; Kalra, Dinesh K; Bolli, Roberto.
Affiliation
  • Tang XL; Institute of Molecular Cardiology, University of Louisville, Louisville, Kentucky, and Institute for Heart Research, Bratislava, Slovakia.
  • Wysoczynski M; Institute of Molecular Cardiology, University of Louisville, Louisville, Kentucky, and Institute for Heart Research, Bratislava, Slovakia.
  • Gumpert AM; Institute of Molecular Cardiology, University of Louisville, Louisville, Kentucky, and Institute for Heart Research, Bratislava, Slovakia.
  • Solanki M; Institute of Molecular Cardiology, University of Louisville, Louisville, Kentucky, and Institute for Heart Research, Bratislava, Slovakia.
  • Li Y; Institute of Molecular Cardiology, University of Louisville, Louisville, Kentucky, and Institute for Heart Research, Bratislava, Slovakia.
  • Wu WJ; Institute of Molecular Cardiology, University of Louisville, Louisville, Kentucky, and Institute for Heart Research, Bratislava, Slovakia.
  • Zheng S; Institute of Molecular Cardiology, University of Louisville, Louisville, Kentucky, and Institute for Heart Research, Bratislava, Slovakia.
  • Ruble H; Institute of Molecular Cardiology, University of Louisville, Louisville, Kentucky, and Institute for Heart Research, Bratislava, Slovakia.
  • Li H; Institute of Molecular Cardiology, University of Louisville, Louisville, Kentucky, and Institute for Heart Research, Bratislava, Slovakia.
  • Stowers H; Institute of Molecular Cardiology, University of Louisville, Louisville, Kentucky, and Institute for Heart Research, Bratislava, Slovakia.
  • Zheng S; Institute of Molecular Cardiology, University of Louisville, Louisville, Kentucky, and Institute for Heart Research, Bratislava, Slovakia.
  • Ou Q; Institute of Molecular Cardiology, University of Louisville, Louisville, Kentucky, and Institute for Heart Research, Bratislava, Slovakia.
  • Tanveer N; Institute of Molecular Cardiology, University of Louisville, Louisville, Kentucky, and Institute for Heart Research, Bratislava, Slovakia.
  • Slezak J; Institute of Molecular Cardiology, University of Louisville, Louisville, Kentucky, and Institute for Heart Research, Bratislava, Slovakia.
  • Kalra DK; Institute of Molecular Cardiology, University of Louisville, Louisville, Kentucky, and Institute for Heart Research, Bratislava, Slovakia.
  • Bolli R; Institute of Molecular Cardiology, University of Louisville, Louisville, Kentucky, and Institute for Heart Research, Bratislava, Slovakia.
Cardiovasc Res ; 2024 Aug 20.
Article in En | MEDLINE | ID: mdl-39163570
ABSTRACT

AIMS:

The development of cell therapy as a widely-available clinical option for ischemic cardiomyopathy is hindered by the invasive nature of current cell delivery methods. Furthermore, the rapid disappearance of cells after transplantation provides a cogent rationale for using repeated cell doses, which, however, has not been done thus far in clinical trials because it is not feasible with invasive approaches. The goal of this translational study was to test the therapeutic utility of the intravenous route for cell delivery. METHODS AND

RESULTS:

Pigs with chronic ischemic cardiomyopathy induced by myocardial infarction received one or three intravenous doses of allogeneic bone marrow mesenchymal stromal cells (MSCs) or placebo 35 days apart. Rigor guidelines, including blinding and randomization, were strictly followed. A comprehensive assessment of LV function was conducted with three independent methods (echocardiography, magnetic resonance imaging, and hemodynamic studies). The results demonstrate that three doses of MSCs improved both load-dependent and independent indices of left ventricular (LV) function and reduced myocardial hypertrophy and fibrosis; in contrast, one dose failed to produce most of these benefits.

CONCLUSIONS:

To our knowledge, this is the first study to show that intravenous infusion of a cell product improves LV function and structure in a large animal model of chronic ischemic cardiomyopathy and that repeated infusions are necessary to produce robust effects. This study, conducted in a clinically-relevant model, supports a new therapeutic strategy based on repeated intravenous infusions of allogeneic MSCs and provides a foundation for a first-in-human trial testing this strategy in patients with chronic ischemic cardiomyopathy.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cardiovasc Res Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cardiovasc Res Year: 2024 Document type: Article Affiliation country: