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Wiley InterScience

American Journal of Transplantation

American Journal of Transplantation

Volume 4 Issue 11, Pages 1776 - 1785

Published Online: 16 Sep 2004

© 2010 American Society of Transplantation and the American Society of Transplant Surgeons



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De Novo Kidney Transplantation Without Use of Calcineurin Inhibitors Preserves Renal Structure and Function at Two Years
Stuart M. Flechner a,*, Sunil M. Kurian b , Kim Solez c , Daniel J. Cook a , James T. Burke d , Hank Rollin a , Jennifer A. Hammond b , Thomas Whisenant b , Caroline M. Lanigan b , Steven R. Head b and Daniel R. Salomon b
  a Section of Renal Transplantation, Transplant Center, and Allogen Laboratories, The Cleveland Clinic Foundation, Cleveland, Ohio, USA
  b DNA Array Core Facility, and the Department of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California, USA
  c Department of Pathology, University of Alberta, Edmonton, Alberta, Canada
  d Transplant Immunology, Wyeth Research, Paris, France
  *Corresponding author: Stuart M. Flechner, flechns@ccf.org

Presented at the American Transplant congress, Boston, Massachusetts, May 16, 2004.

Copyright Blackwell Munksgaard 2004
KEYWORDS
Chronic allograft nephropathy • gene expression • kidney transplantation • sirolimus

ABSTRACT

We performed a randomized prospective trial comparing calcineurin inhibitor (CNI)-free to CNI-based immunosuppression to determine the impact on renal function, structure and gene expression. Sixty-one kidney recipients treated with basiliximab mycophenolate mofetil (MMF) and prednisone (P) were randomly assigned to concentration-controlled sirolimus or cyclosporine. Two years post-transplant 55 patients underwent renal function studies, 48 (87%) underwent transplant biopsies; all classified by Banff scoring and 41 by DNA microarrays. Comparing sirolimus/MMF/P to cyclosporine/MMF/P there was a significantly lower serum creatinine (1.35 vs. 1.81 mg/dL; p = 0.008), higher Cockroft-Gault glomerular filtration rate (GFR) (80.4 vs. 63.4 mL/min; p = 0.008), iothalamate GFR (60.6 vs. 49.2 mL/min; p = 0.018) and Banff 0 (normal) biopsies (66.6 vs. 20.8%; p = 0.013). Regression analysis of calculated GFRs from 1 to 36 months yielded a positive slope for sirolimus of 3.36 mL/min/year, and a negative slope for cyclosporine of −1.58 mL/min/year (p = 0.008). Gene expression profiles from kidneys with higher Banff chronic allograft nephropathy (CAN) scores confirmed significant up-regulation of genes responsible for immune/inflammation and fibrosis/tissue remodeling. At 2 years the sirolimus-treated recipients have better renal function, a diminished prevalence of CAN and down-regulated expression of genes responsible for progression of CAN. All may provide for an alternative natural history with improved graft survival.


Received 19 May 2004, revised and accepted for publication 28 July 2004

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1600-6143.2004.00627.x About DOI

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