Author/Authors :
Joseph، نويسنده , , Jacob and Rimawi، نويسنده , , Asem and Mehta، نويسنده , , Paulette and Cottler-Fox، نويسنده , , Michele and Sinha، نويسنده , , Anjan and Singh، نويسنده , , Balkrishnaman K. and Pacheco، نويسنده , , Rebecca and Smith III، نويسنده , , Eugene S. and Mehta، نويسنده , , Jawahar L.، نويسنده ,
Abstract :
The objective of this study was to determine a safe and effective dose of granulocyte-colony stimulating factor (G-CSF) to mobilize hematopoietic stem cells in patients with advanced heart failure and to determine its effects on the cytokine profile. Patients with advanced heart failure (n = 6) and implantable defibrillators in situ were administered G-CSF after baseline echocardiographic and laboratory evaluation, using an escalating dose schedule designed to ensure safety. The peripheral CD34+ hematopoietic stem cell count increased from 3.6 ± 0.5/μl to 38.7 ± 13/μl (p = 0.022) after 5 days of 5 μg/kg/day G-CSF therapy. The baseline or peak white blood cell count did not predict the stem cell response. G-CSF increased plasma levels of interleukin-10. Left ventricular ejection fraction increased significantly in the 4 patients with ischemic cardiomyopathy 9 months after treatment. No major adverse effects attributable to the drug occurred during administration or 9 months of follow-up. Our results have shown that low-dose G-CSF significantly mobilized hematopoietic stem cells in advanced heart failure and improved left ventricular function in the ischemic subset of patients. G-CSF significantly increased plasma levels of the anti-inflammatory cytokine interleukin-10, without changing pro-inflammatory cytokine levels. In conclusion, these results indicate a novel mechanism of action for the potential therapeutic benefit of G-CSF in advanced ischemic cardiomyopathy.