Waiser Johannes, Schneider Michael, Eljazyfer Sara, Slowinski Torsten, Glander Petra, Einecke Gunilla, Budde Klemens, Neumayer Hans-Hellmut, Böhler Torsten
Department of Internal Medicine-Nephrology, University Hospital Charité, Campus Mitte, Schumannstrasse 20/21, 10117 Berlin, Germany.
Clin Immunol. 2006 Apr;119(1):59-66. doi: 10.1016/j.clim.2005.12.006. Epub 2006 Jan 31.
Profibrotic cytokines such as transforming growth factor-beta 1 (TGF-beta1) and endothelin-1 (ET-1) are involved in the pathogenesis of chronic allograft nephropathy. We assessed the effect of maintenance immunosuppression with or without cyclosporine A on TGF-beta1 and ET-1 expression as well as lymphocyte proliferation in renal allograft recipients. Patients were divided into groups according to their maintenance immunosuppression: A, azathioprine + methylprednisolone; B, cyclosporine A + azathioprine + methylprednisolone. TGF-beta1 and ET-1 plasma concentrations were not different between both groups. TGF-beta1 concentrations in cell culture supernatants and lymphocyte proliferation were higher in group B as compared to group A. No correlation was found between TGF-beta1 plasma concentrations and lymphocyte proliferation. Multiple linear regression analysis revealed that patient characteristics influence TGF-beta1 and ET-1 expression. In conclusion, plasma levels of profibrotic cytokines do not reflect the existing profibrotic potential of immunosuppressive drugs. Demographic factors and the employed co-medication confound the results.