Dialyse aktuell 2014; 18(4): 204-209
DOI: 10.1055/s-0034-1381225
Transplantation
© Georg Thieme Verlag Stuttgart · New York

Nachsorge nach Nierentransplantation – Welche Immunsuppression ist für welche Patienten im Langzeitverlauf geeignet?

Follow-up care after renal transplantation – Which immunosuppression is suited for which patients in long-term follow-up?
Lutz Renders
1   Abteilung für Nephrologie, II. Medizinische Klinik und Poliklinik, Klinikum rechts der Isar, Technische Universität München (Leitung: Univ.-Prof. Dr. Dr. h. c. Uwe Heemann)
,
Konrad Stock
1   Abteilung für Nephrologie, II. Medizinische Klinik und Poliklinik, Klinikum rechts der Isar, Technische Universität München (Leitung: Univ.-Prof. Dr. Dr. h. c. Uwe Heemann)
,
Dominik Steubl
1   Abteilung für Nephrologie, II. Medizinische Klinik und Poliklinik, Klinikum rechts der Isar, Technische Universität München (Leitung: Univ.-Prof. Dr. Dr. h. c. Uwe Heemann)
,
Wen Ming
1   Abteilung für Nephrologie, II. Medizinische Klinik und Poliklinik, Klinikum rechts der Isar, Technische Universität München (Leitung: Univ.-Prof. Dr. Dr. h. c. Uwe Heemann)
,
Klaus Thürmel
1   Abteilung für Nephrologie, II. Medizinische Klinik und Poliklinik, Klinikum rechts der Isar, Technische Universität München (Leitung: Univ.-Prof. Dr. Dr. h. c. Uwe Heemann)
,
Claudius Küchle
1   Abteilung für Nephrologie, II. Medizinische Klinik und Poliklinik, Klinikum rechts der Isar, Technische Universität München (Leitung: Univ.-Prof. Dr. Dr. h. c. Uwe Heemann)
,
Christoph Schmaderer
1   Abteilung für Nephrologie, II. Medizinische Klinik und Poliklinik, Klinikum rechts der Isar, Technische Universität München (Leitung: Univ.-Prof. Dr. Dr. h. c. Uwe Heemann)
› Author Affiliations
Further Information

Publication History

Publication Date:
15 May 2014 (online)

Die Wahl der Immunsuppression im Langzeitverlauf nach Nierentransplantation ist nach wie vor eine Herausforderung für jeden Nephrologen. Nach dem Beginn mit einer Tripelimmunsuppression bestehend aus einem Calcineurininhibitor, Mycophenolsäure und Steroiden ohne oder mit zusätzlicher Induktionstherapie gibt es viele Gründe für eine Modifikation der eingesetzten Medikamente. Dazu gehören eine Über- oder Unterimmunsuppression, die zu Korrekturen führen muss. Nicht selten zwingen aber Nebenwirkungen der Medikamente selbst, Infekte oder das Auftreten von Antikörpern zu einer Veränderung der Therapie. Ziel bleibt immer die Gesamtmenge der Immunsuppression möglichst niedrig zu halten, was aber in Zeiten komplexerer Patienten mit jetzt häufigerem Auftreten von Antikörpern und auch z. T. schlechterer Organangebote nicht immer gelingen kann.

Today, immunosuppressive therapy in the long-term after kidney transplantation is influenced by many factors. Starting with a triple therapy including calcineurin inhibitors, mycophenol acid and steroids with or without induction therapy, many patients need an adjustment of their immunosuppressive drugs. Adverse events, infections or antibodies before and after transplantation lead to specific changes of the drug therapy. Nevertheless, the main aim is to reduce immunosuppression to a level as low as possible. Unfortunately, older organs and patients' history sometimes are limitations for this step.

 
  • Literatur

  • 1 Rostaing L, Vincenti F, Grinyo J et al. Long-term belatacept exposure maintains efficacy and safety at 5 years: results from the long-term extension of the BENEFIT study. Am J Transplant 2013; 13: 2875-2883
  • 2 Pestana JO, Grinyo JM, Vanrenterghem Y et al. Three-year outcomes from BENEFIT-EXT: a phase III study of belatacept versus cyclosporine in recipients of extended criteria donor kidneys. Am J Transplant 2012; 12: 630-639
  • 3 Larsen CP, Grinyo J, Medina-Pestana J et al. Belatacept-based regimens versus a cyclosporine A-based regimen in kidney transplant recipients: 2-year results from the BENEFIT and BENEFIT-EXT studies. Transplantation 2010; 90: 1528-1535
  • 4 Durrbach A, Pestana JM, Pearson T et al. A phase III study of belatacept versus cyclosporine in kidney transplants from extended criteria donors (BENEFIT-EXT study). Am J Transplant 2010; 10: 547-557
  • 5 Nankivell BJ, Fenton-Lee CA, Kuypers DR et al. Effect of histological damage on long-term kidney transplant outcome. Transplantation 2001; 71: 515-523
  • 6 Nankivell BJ, Borrows RJ, Fung CL et al. The natural history of chronic allograft nephropathy. N Engl J Med 2003; 349: 2326-2333
  • 7 Larson TS, Dean PG, Stegall MD et al. Complete avoidance of calcineurin inhibitors in renal transplantation: a randomized trial comparing sirolimus and tacrolimus. Am J Transplant 2006; 6: 514-522
  • 8 Matas AJ. Chronic progressive calcineurin nephrotoxicity: an overstated concept. Am J Transplant 2011; 11: 687-692
  • 9 Budde K, Lehner F, Sommerer C et al. ZEUS Study Investigators. Conversion from cyclosporine to everolimus at 4.5 months posttransplant: 3-year results from the randomized ZEUS study. Am J Transplant 2012; 12: 1528-1540
  • 10 Schena FP, Pascoe MD, Alberu J et al. Sirolimus CONVERT Trial Study Group. Conversion from calcineurin inhibitors to sirolimus maintenance therapy in renal allograft recipients: 24-month efficacy and safety results from the CONVERT trial. Transplantation 2009; 87: 233-242
  • 11 Abramowicz D, Del Carmen Rial M, Vitko S et al. Cyclosporine Withdrawal Study Group. Cyclosporine withdrawal from a mycophenolate mofetil-containing immunosuppressive regimen: results of a five-year, prospective, randomized study. J Am Soc Nephrol 2005; 16: 2234-2240
  • 12 Chhabra D, Alvarado A, Dalal P et al. Impact of calcineurin-inhibitor conversion to mTOR inhibitor on renal allograft function in a prednisone-free regimen. Am J Transplant 2013; 13: 2902-2911
  • 13 Nashan B. Induction therapy and mTOR inhibition: minimizing calcineurin inhibitor exposure in de novo renal transplant patients. Clinical transplantation 2013; 27 (Suppl. 25) 16-29
  • 14 Kasiske BL, Snyder JJ, Gilbertson D, Matas AJ. Diabetes mellitus after kidney transplantation in the United States. Am J Transplant 2003; 3: 178-185
  • 15 Silva Jr HT, Yang HC, Meier-Kriesche HU et al. Long-term follow-up of a phase III clinical trial comparing tacrolimus extended-release/MMF, tacrolimus/MMF, and cyclosporine/MMF in de novo kidney transplant recipients. Transplantation 2014; 97: 636-641
  • 16 Miles AM, Sumrani N, Horowitz R et al. Diabetes mellitus after renal transplantation: as deleterious as non-transplant-associated diabetes?. Transplantation 1998; 65: 380-384
  • 17 Hayer MK, Farrugia D, Begaj I et al. Infection-related mortality is higher for kidney allograft recipients with pretransplant diabetes mellitus. Diabetologia 2014; 57: 554-561
  • 18 Webster AC, Woodroffe RC, Taylor RS et al. Tacrolimus versus ciclosporin as primary immunosuppression for kidney transplant recipients: meta-analysis and meta-regression of randomised trial data. BMJ 2005; 331: 810-810
  • 19 Hecking M, Kainz A, Werzowa J et al. Glucose metabolism after renal transplantation. Diabetes Care 2013; 36: 2763-2771
  • 20 Pietruck F, Kribben A, Van TN et al. Rosiglitazone is a safe and effective treatment option of new-onset diabetes mellitus after renal transplantation. Transplant Int 2005; 18: 483-486
  • 21 Werzowa J, Hecking M, Haidinger M et al. Vildagliptin and pioglitazone in patients with impaired glucose tolerance after kidney transplantation: a randomized, placebo-controlled clinical trial. Transplantation 2013; 95: 456-462
  • 22 Pinelli NR, Nemerovski CW, Koelling TM. Successful long-term use of sitagliptin for the treatment of new-onset diabetes mellitus after solid organ transplantation: a case report. Transplant Proc 2011; 43: 2113-2115
  • 23 Lane JT, Odegaard DE, Haire CE et al. Sitagliptin therapy in kidney transplant recipients with new-onset diabetes after transplantation. Transplantation 2011; 92
  • 24 Haidinger M, Werzowa J, Hecking M et al. Efficacy and safety of vildagliptin in new-onset diabetes after kidney transplantation--a randomized, double-blind, placebo-controlled trial. Am J Transplant 2014; 14: 115-123
  • 25 Blanckaert K, De Vriese AS. Current recommendations for diagnosis and management of polyoma BK virus nephropathy in renal transplant recipients. Nephrol Dial Transplant 2006; 21: 3364-3367
  • 26 Suwelack B, Malyar V, Koch M et al. The influence of immunosuppressive agents on BK virus risk following kidney transplantation, and implications for choice of regimen. Transplant Rev (Orlando) 2012; 26: 201-211
  • 27 Johnston O, Jaswal D, Gill JS et al. Treatment of polyomavirus infection in kidney transplant recipients: a systematic review. Transplantation 2010; 89: 1057-1070
  • 28 Zaman RA, Ettenger RB, Cheam H et al. A novel treatment regimen for BK viremia. Transplantation [Epub ahead of print] 13.02.2014;
  • 29 Lee BT, Gabardi S, Grafals M et al. Efficacy of levofloxacin in the treatment of BK viremia: a multicenter, double-blinded, randomized, placebo-controlled trial. Clin J Am Soc Nephrol 2014; 9: 583-589
  • 30 Renders L, Heemann U. Chronic renal allograft damage after transplantation: what are the reasons, what can we do?. Curr Opin Organ Transplant 2012; 17: 634-639
  • 31 Hardinger KL, Brennan DC. Novel immunosuppressive agents in kidney transplantation. World J Transplant 2013; 3: 68-77
  • 32 Douzdjian V, Rice JC, Carson RW et al. Renal retransplants: effect of primary allograft nephrectomy on early function, acute rejection and outcome. Clin Transplant 1996; 10: 203-208
  • 33 Del Bello A, Rostaing L, Congy-Jolivet N et al. [Kidney nephrectomy after allograft failure]. Nephrol Ther 2013; 9: 189-194