1. Monitoring of human cytomegalovirus, HHV-6 and HHV-7 infection in kidney transplant recipients by molecular methods to predict HCMV disease after transplantation: a prospective study.
- Author
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Rayes N, Seehofer D, Lullius SG, Stein A, May G, Kahl A, Frei U, Neuhaus P, and Meisel H
- Subjects
- Cytomegalovirus genetics, Cytomegalovirus Infections etiology, DNA, Viral blood, Humans, Phosphoproteins blood, Polymerase Chain Reaction, Population Surveillance, Postoperative Period, Prevalence, Prospective Studies, RNA, Messenger blood, Risk Factors, Roseolovirus Infections epidemiology, Sensitivity and Specificity, Serologic Tests, Viral Load, Viral Matrix Proteins blood, Cytomegalovirus Infections diagnosis, Genetic Techniques, Herpesvirus 6, Human, Herpesvirus 7, Human, Kidney Transplantation, Pancreas Transplantation, Roseolovirus Infections diagnosis
- Abstract
Objectives: Recently, highly sensitive molecular assays to detect HCMV, HHV-6 and HHV-7 have been developed but their ability to detect patients at high risk for disease is unclear., Methods: The positive predictive values (PPV) of pp65-antigenemia, quantitative plasma DNA and pp67-mRNA for CMV-disease were prospectively compared in 82 transplant recipients (72 renal, 10 pancreas-kidney) without CMV-prophylaxis. In addition, the prevalence of HHV-6 and HHV-7 infection were assessed using qualitative PCR. The assays were performed weekly., Results: Three patients (3,7%) developed CMV-disease and were effectively treated. They were positive in all three CMV-assays. The PPVs of pp65-Ag, DNA viral load and pp67-mRNA were 33%, 20% and 25% in CMV-positive and 100%, 67% and 50% in seronegative recipients. Sensitivity and negative predictive value were 100% for all assays. Using cut-offs, PPVs were 75% (pp65-Ag > or = 20/200.000 cells) and 100% (PCR > or =30.000 copies/ml). Transfusion of >2 packed red cells, rejection and non-functioning graft were risk factors for CMV Five patients and one patient were positive for HHV-6 and HHV-7 resp.; both were symptomless and did not have a HCMV infection., Conclusions: Therefore, pp65-antigenemia and plasma PCR with a cut-off could be useful for monitoring preemptive therapy.
- Published
- 2005