The time window for therapy with peptide nanofibers combined with autologous bone marrow cells in pigs after acute myocardial infarction

PLoS One. 2015 Mar 10;10(3):e0115430. doi: 10.1371/journal.pone.0115430. eCollection 2015.

Abstract

Background: We previously showed that injection of peptide nanofibers (NF) combined with autologous bone marrow mononuclear cells (MNC) immediately after coronary artery ligation improves cardiac performance in pigs. To evaluate the clinical feasibility, this study was performed to determine the therapeutic time window for NF/MNC therapy in acute myocardial infarction (MI).

Methods and results: A total of 45 adult minipigs were randomly grouped into 7 groups: sham or MI plus treatment with NS (normal saline), or NF or MNC alone at 1 day (1D) post-MI, or NF/MNC at 1, 4, or 7 days post-MI (N≥6). Cardiac function was assessed by echocardiography and ventricular catheterization. Compared with the NS control, pigs treated with NF/MNC at 1 day post-MI (NF/MC-1D) had the greatest improvement in left ventricle ejection fraction (LVEF; 55.1±1.6%; P<0.01 vs. NS) 2 months after MI. In contrast, pigs treated with either NF/MNC-4D or NF/MNC-7D showed 48.9±0.8% (P<0.05 vs. NS) and 43.5±2.3% (n.s. vs. NS) improvements, respectively. The +dP/dt and -dP/dt, infarct size and interstitial collagen content were also improved in the NF/MNC-1D and -4D groups but not in the -7D group. Mechanistically, MNC quality and the states of systemic inflammation and damaged heart tissue influence the therapeutic efficiency of NF/MNC therapy, as revealed by another independent study using 16 pigs.

Conclusions: Injection of NF/MNC at 1 or 4 days, but not at 7 days post-MI, improves cardiac performance and prevents ventricular remodeling, confirming the importance of early intervention when using this therapy for acute MI.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Marrow Transplantation
  • Cell Differentiation
  • Drug Administration Schedule
  • Endothelial Cells / physiology
  • Endothelium, Vascular / pathology
  • Myocardial Infarction / pathology
  • Myocardial Infarction / therapy*
  • Myocardium / pathology
  • Nanofibers / therapeutic use*
  • Peptides / therapeutic use
  • Swine
  • Swine, Miniature
  • Time Factors
  • Transplantation, Autologous
  • Ventricular Remodeling

Substances

  • Peptides

Grants and funding

This work was supported by the National Research Program for Biopharmaceuticals (DOH101-TD-PB-111-TM027 and DOH101-TD-PB-111-TM028), the National Science Council (NSC101-2325-B-006-013), the National Health Research Institutes (NHRI-EX101-10026SI), the Academia Sinica Translational Medicine Program and Celgene Cellular Therapeutics and Meridigen Biotech Co. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.