Key result
Delayed intracoronary stem cell therapy reduces indexed end-diastolic volume by ~23 ml/m2 vs control in post-MI swine.
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Demonstrates that 7-day delayed cardiac stem cell delivery curbs adverse ventricular remodeling in swine, indicating optimal timing enhances post-infarction structural repair.
BACKGROUND: 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. METHODS: Female swine surviving 90 min occlusion of the mid left anterior descending coronary artery received an intracoronary injection of 25x10(6) 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. RESULTS: No 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/m(2) ± 26.09 ml/m(2), D7: 98.71 ml/m(2) ± 8.30 ml/m(2), 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. CONCLUSIONS: The intracoronary injection of 25x10(6) 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.
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Crisóstomo et al. (2015) studied Experimental acute myocardial infarction (closed-chest ischemia-reperfusion model in swine) (n=17). Intracoronary allogeneic porcine cardiac stem cells (same-day or 7-day delayed delivery) vs. Intracoronary vehicle injection on day 7 was evaluated on Indexed End Diastolic Volume (ml/m2) at 10 weeks (D7 vs Control) (p=0.037). Delayed (day 7) intracoronary allogeneic cardiac stem cell therapy significantly reduced indexed end-diastolic volume vs control in post-MI swine (98.71 vs 121.70 ml/m2, p=0.037).
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