Abstract

BackgroundThe optimal timing of cardiac stem cells administration is still unclear. We assessed the safety of same-day and delayed (one week) delivery and the possible influence of the timing on the therapeutic outcomes of allogeneic porcine cardiac stem cells administration after acute myocardial infarction in a closed-chest ischemia-reperfusion model.MethodsFemale swine surviving 90 min occlusion of the mid left anterior descending coronary artery received an intracoronary injection of 25x106 porcine cardiac stem cells either two hours (n = 5, D0) or 7 days (n = 6, D7) after reperfusion. Controls received intracoronary injection of vehicle on day 7 (n = 6, CON). Safety was defined in terms of absence of major cardiac events, changes to the ECG during injection, post-administration coronary flow assessed using the TIMI scale and cardiac troponin I determination after the intervention. Cardiac Magnetic Resonance was performed for morphological and functional assessment prior to infarction, before injection (D7 and CON groups only), at one and 10 weeks. Samples were taken from the infarct and transition areas for pathological examination.ResultsNo major adverse cardiac events were seen during injection in any group. Animals receiving the therapy on the same day of infarction (D0 group) showed mild transient ST changes during injection (n = 4) and, in one case, slightly compromised coronary flow (TIMI 2). Cardiac function parameters and infarct sizes were not significantly different between groups, with a trend towards higher ejection fraction in the treated groups. Ventricular volumes indexed to body surface area increased over time in control animals, and decreased by the end of the study in animals receiving the therapy, significantly so when comparing End Diastolic Volume between CON and D7 groups (CON: 121.70 ml/m2 ± 26.09 ml/m2, D7: 98.71 ml/m2 ± 8.30 ml/m2, p = 0.037). The treated groups showed less organization of the collagenous scar, and a significantly (p = 0.019) higher amount of larger, more mature vessels at the infarct border.ConclusionsThe intracoronary injection of 25x106 allogeneic cardiac stem cells is generally safe, both early and 7 days after experimental infarction, and alleviates myocardial dysfunction, with a greater limitation of left ventricular remodeling when performed at one week.Electronic supplementary materialThe online version of this article (doi:10.1186/s12967-015-0512-2) contains supplementary material, which is available to authorized users.

Highlights

  • The optimal timing of cardiac stem cells administration is still unclear

  • One of the animals died during infarct induction, before group allocation, and a second animal belonging to D0 died during the stabilizing period, prior to porcine CSCs (pCSCs) administration

  • Our findings following the intracoronary injection of 25x106 confirm the safety of this approach, both early and 7 days after experimental acute myocardial infarction (AMI), with no major adverse cardiac events (MACEs) during administration or later cardiac deaths seen in any animal

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Summary

Introduction

The optimal timing of cardiac stem cells administration is still unclear. We assessed the safety of same-day and delayed (one week) delivery and the possible influence of the timing on the therapeutic outcomes of allogeneic porcine cardiac stem cells administration after acute myocardial infarction in a closed-chest ischemia-reperfusion model. Cardiac stem cells (CSCs) have been proved in numerous preclinical studies to improve left ventricular function and attenuate remodeling after myocardial infarction [4,5,6,7,8,9,10,11,12]. Based on these experimental works, human trials have been initiated. Once the inflammatory phase is over, scar formation and adverse remodeling are under way, and the effect of the cells may be limited [29], there are studies reporting beneficial effects at subacute and chronic settings [30, 31]

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