PLoS ONE (Jan 2020)

Kinetics of cytomegalovirus and Epstein-Barr virus DNA in whole blood and plasma of kidney transplant recipients: Implications on management strategies.

  • Tiziana Lazzarotto,
  • Angela Chiereghin,
  • Antonio Piralla,
  • Dino Gibertoni,
  • Giulia Piccirilli,
  • Gabriele Turello,
  • Giulia Campanini,
  • Liliana Gabrielli,
  • Cristina Costa,
  • Giorgia Comai,
  • Gaetano La Manna,
  • Luigi Biancone,
  • Teresa Rampino,
  • Marilena Gregorini,
  • Francesca Sidoti,
  • Gabriele Bianco,
  • Maria Vittoria Mauro,
  • Francesca Greco,
  • Rossana Cavallo,
  • Fausto Baldanti,
  • AMCLI-GLaIT

DOI
https://doi.org/10.1371/journal.pone.0238062
Journal volume & issue
Vol. 15, no. 8
p. e0238062

Abstract

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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.