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Zytomegalievirusinfektion nach Nierentransplantation

Cytomegalovirus infection after renal transplantation

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Der Nephrologe Aims and scope

Zusammenfassung

Die CMV-Infektion gehört zu den häufigsten und am meisten Ressourcen verbrauchenden Infektionskomplikationen nach Nierentransplantation. Die Durchseuchung ist hoch, das Virus persistiert lebenslang. Unter Immunsuppression kann es zur Reaktivierung kommen, seronegative Empfänger können durch das Transplantat neu infiziert werden. Goldstandard der Diagnostik ist der Nachweis von pp65 in Leukozyten oder der Virus-DNA im Blut, die Serologie dient ausschließlich der Risikostratifizierung des Patienten vor Transplantation. Die CMV-Erkrankung kann heute überwiegend verhindert werden: Die „Prophylaxestrategie“ besteht aus Ganciclovir oder Valganciclovir über 90 bis 100 Tage, bei der „präemptiven Therapie“ (Voraussetzung: engmaschiges CMV-DNA-Monitoring) wird erst bei nachgewiesener Replikation behandelt, vor Auftreten von Symptomen. Eine CMV-Erkrankung kommt nur noch selten vor und muss rasch antiviral, ggf. auch mit Hyperimmunglobulinen behandelt werden.

Abstract

Cytomegalovirus (CMV) infections are among the most frequent and resource consuming infectious complications after renal transplantation. The prevalence of latent infection is high and the virus shows life-long persistence. Immunosuppressive therapy may lead to virus reactivation and seronegative recipients may be infected via transplanted kidneys from a seropositive donor. Detection of pp65 in leukocytes or viral DNA in blood is the diagnostic gold standard and serology can only be used to establish the risk stratification prior to transplantation. Two different strategies aim at protecting the patient from overt disease. The strategy of prophylaxis relies on 90-100 days of ganciclovir or valganciclovir, the“preemptive therapy” uses antiviral treatment only after viral DNA is detected in blood, but ideally before disease occurs. This strategy depends on frequent DNA testing. If CMV disease is diagnosed, rapid antiviral and in some cases also immunoglobulin therapy are mandatory.

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Literaturverzeichnis

  1. Babel N, Gabdrakhmanova L, Juergensen JS et al. (2004) Treatment of cytomegalovirus disease with valganciclovir in renal transplant recipients: a single center experience. Transplantation 78: 283–285

    Article  PubMed  CAS  Google Scholar 

  2. Bowden RA, Slichter SJ, Sayers M et al. (1995) A comparison of filtered leukocyte-reduced and cytomegalovirus (CMV) seronegative blood products for the prevention of transfusion-associated CMV infection after marrow transplant. Blood 86: 3598–3603

    PubMed  CAS  Google Scholar 

  3. Bunde T, Kirchner A, Hoffmeister B et al. (2005) Protection from cytomegalovirus after transplantation is correlated with immediate early 1-specific CD8 T cells. J Exp Med 201: 1031–1036

    Article  PubMed  CAS  Google Scholar 

  4. de Ory F, Ramirez R, Garcia CL et al. (2004) Is there a change in cytomegalovirus seroepidemiology in Spain? Eur J Epidemiol 19: 85–89

    Google Scholar 

  5. Doyle AM, Warburton KM, Goral S et al. (2006) 24-week oral ganciclovir prophylaxis in kidney recipients is associated with reduced symptomatic cytomegalovirus disease compared to a 12-week course. Transplantation 81: 1106–1111

    Article  PubMed  CAS  Google Scholar 

  6. Flechner SM, Avery RK, Fisher R et al. (1998) A randomized prospective controlled trial of oral acyclovir versus oral ganciclovir for cytomegalovirus prophylaxis in high-risk kidney transplant recipients. Transplantation 66: 1682–1688

    Article  PubMed  CAS  Google Scholar 

  7. Franquet T, Lee KS, Muller NL (2003) Thin-section CT findings in 32 immunocompromised patients with cytomegalovirus pneumonia who do not have AIDS. AJR Am J Roentgenol 181: 1059–1063

    PubMed  Google Scholar 

  8. Gomez E, de OM, Aguado S et al. (1996) Cytomegalovirus preemptive therapy with ganciclovir in renal transplant patients treated with OKT3. Nephron 74: 367–372

    Article  PubMed  CAS  Google Scholar 

  9. Hengster P, Pescovitz MD, Hyatt D, Margreiter R (1999) Cytomegalovirus infections after treatment with daclizumab, an anti IL-2 receptor antibody, for prevention of renal allograft rejection. Roche Study Group. Transplantation 68: 310–313

    Article  PubMed  CAS  Google Scholar 

  10. Hibberd PL, Tolkoff-Rubin NE, Cosimi AB et al. (1992) Symptomatic cytomegalovirus disease in the cytomegalovirus antibody seropositive renal transplant recipient treated with OKT3. Transplantation 53: 68–72

    Article  PubMed  CAS  Google Scholar 

  11. Khoury JA, Storch GA, Bohl DL et al. (2006) Prophylactic versus preemptive oral valganciclovir for the management of cytomegalovirus infection in adult renal transplant recipients. Am J Transplant 6: 2134–2143

    Article  PubMed  CAS  Google Scholar 

  12. Limaye AP, Corey L, Koelle DM et al. (2000) Emergence of ganciclovir-resistant cytomegalovirus disease among recipients of solid-organ transplants. Lancet 356: 645–649

    Article  PubMed  CAS  Google Scholar 

  13. Lowance D, Neumayer HH, Legendre CM et al. (1999) Valacyclovir for the prevention of cytomegalovirus disease after renal transplantation. International Valacyclovir Cytomegalovirus Prophylaxis Transplantation Study Group. N Engl J Med 340: 1462–1470

    Article  PubMed  CAS  Google Scholar 

  14. McLaughlin K, Sandhu S, Wu C et al. (2005) Transplanting kidneys from CMV-seropositive donors to CMV-seronegative recipients is not associated with poorer renal allograft function or survival. Nephrol Dial Transplant 20: 176–180

    Article  PubMed  Google Scholar 

  15. Mocarski ES Jr (2004) Immune escape and exploitation strategies of cytomegaloviruses: impact on and imitation of the major histocompatibility system. Cell Microbiol 6: 707–717

    Article  PubMed  CAS  Google Scholar 

  16. Paya C, Humar A, Dominguez E et al. (2004) Efficacy and safety of valganciclovir vs. oral ganciclovir for prevention of cytomegalovirus disease in solid organ transplant recipients. Am J Transplant 4: 611–620

    Article  PubMed  CAS  Google Scholar 

  17. Sagedal S, Nordal KP, Hartmann A et al. (2000) A prospective study of the natural course of cytomegalovirus infection and disease in renal allograft recipients. Transplantation 70: 1166–1174

    Article  PubMed  CAS  Google Scholar 

  18. Sagedal S, Nordal KP, Hartmann A et al. (2003) Pre-emptive therapy of CMVpp65 antigen positive renal transplant recipients with oral ganciclovir: a randomized, comparative study. Nephrol Dial Transplant 18: 1899–1908

    Article  PubMed  CAS  Google Scholar 

  19. Sagedal S, Rollag H, Hartmann A (2007) Cytomegalovirus infection in renal transplant recipients is associated with impaired survival irrespective of expected mortality risk. Clin Transplant 21: 309–313

    Article  PubMed  Google Scholar 

  20. Sester M, Sester U, Gartner B et al. (2001) Levels of virus-specific CD4 T cells correlate with cytomegalovirus control and predict virus-induced disease after renal transplantation. Transplantation 71: 1287–1294

    Article  PubMed  CAS  Google Scholar 

  21. Smiley ML, Wlodaver CG, Grossman RA et al. (1985) The role of pretransplant immunity in protection from cytomegalovirus disease following renal transplantation. Transplantation 40: 157–161

    Article  PubMed  CAS  Google Scholar 

  22. Strippoli GF, Hodson EM, Jones C, Craig JC (2006) Preemptive treatment for cytomegalovirus viremia to prevent cytomegalovirus disease in solid organ transplant recipients. Transplantation 81: 139–145

    Article  PubMed  Google Scholar 

  23. The EBPG Expert Group on Haemodialysis (2000) European Best Practice Guidelines for Renal Transplantation (part 1). Nephrol Dial Transplant 15 (Suppl 7) 15: 1–85

    Google Scholar 

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Interessenkonflikt

Der Autor erhält wissenschaftliche Projektfinanzierung sowie Vortragshonorare von folgenden Firmen: Amgen GmbH, Hoffmann La Roche AG, Gambro GmbH.

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Correspondence to M. Girndt.

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Girndt, M. Zytomegalievirusinfektion nach Nierentransplantation. Nephrologe 3, 51–62 (2008). https://doi.org/10.1007/s11560-007-0140-9

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  • DOI: https://doi.org/10.1007/s11560-007-0140-9

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