Abstract

This retrospective multicenter cohort study investigated the kinetics (ascending and descending phases) of cytomegalovirus (CMV) and Epstein-Barr virus (EBV)-DNA in whole blood (WB) and plasma samples collected from adult kidney transplant (KT) recipients. CMV-DNA kinetics according to antiviral therapy were investigated. Three hundred twenty-eight paired samples from 42 episodes of CMV infection and 157 paired samples from 26 episodes of EBV infection were analyzed by a single commercial molecular method approved by regulatory agencies for both matrices. CMV-DNAemia followed different kinetics in WB and plasma. In the descending phase of infection, a slower decay of viral load and a higher percentage of CMV-DNA positive samples were observed in plasma versus WB. In the 72.4% of patients receiving antiviral therapy, monitoring with plasma CMV-DNAemia versus WB CMV-DNAemia could delay treatment interruption by 7–14 days. Discontinuation of therapy based on WB monitoring did not result in relapsed infection in any patients. Highly different EBV-DNA kinetics in WB and plasma were observed due to lower positivity in plasma; EBV positive samples with a quantitative result in both blood compartments were observed in only 11.5% of cases. Our results emphasize the potential role of WB as specimen type for post-KT surveillance of both infections for disease prevention and management.

Highlights

  • Cytomegalovirus (CMV) and Epstein-Barr virus (EBV) have a central role in kidney transplant recipients (KTRs) [1]

  • We investigated the kinetics of both viruses in whole blood (WB) and plasma samples collected from adult KTRs

  • The total number of paired samples investigated for the search of CMV and EBV-DNA was 328 and 157, respectively; the median number of sequential paired samples tested per infection episode was 7

Read more

Summary

Introduction

Cytomegalovirus (CMV) and Epstein-Barr virus (EBV) have a central role in kidney transplant recipients (KTRs) [1]. In solid organ transplant (SOT), kinetics analyses have never been performed of CMV and EBV-DNAemia in WB and plasma using a single, approved molecular method for quantifying CMV and EBV-DNA in both blood matrices. In a previous study [6], we investigated the kinetics of both CMV and EBV-DNAemia in WB and plasma collected from pediatric and adult allogeneic hematopoietic stem cell transplant (HSCT) recipients using a CE-marked and FDA-approved automated molecular method. These data demonstrated that CMV and EBV-DNAemia follow different kinetics in the two blood compartments in HSCT [6]. These observations may impact monitoring, prophylactic and therapeutic management strategies for these infections

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call