PLoS ONE (Jan 2018)

Plasma donor-derived cell-free DNA kinetics after kidney transplantation using a single tube multiplex PCR assay.

  • Els M Gielis,
  • Charlie Beirnaert,
  • Amélie Dendooven,
  • Pieter Meysman,
  • Kris Laukens,
  • Joachim De Schrijver,
  • Steven Van Laecke,
  • Wim Van Biesen,
  • Marie-Paule Emonds,
  • Benedicte Y De Winter,
  • Jean-Louis Bosmans,
  • Jurgen Del Favero,
  • Daniel Abramowicz,
  • Kristien J Ledeganck

DOI
https://doi.org/10.1371/journal.pone.0208207
Journal volume & issue
Vol. 13, no. 12
p. e0208207

Abstract

Read online

BackgroundAfter transplantation, cell-free DNA derived from the donor organ (ddcfDNA) can be detected in the recipient's circulation. We aimed to quantify ddcfDNA levels in plasma of kidney transplant recipients thereby investigating the kinetics of this biomarker after transplantation and determining biological variables that influence ddcfDNA kinetics in stable and non-stable patients.Materials and methodsFrom 107 kidney transplant recipients, plasma samples were collected longitudinally after transplantation (day 1-3 months) within a multicenter set-up. Cell-free DNA from the donor was quantified in plasma as a fraction of the total cell-free DNA by next generation sequencing using a targeted, multiplex PCR-based method for the analysis of single nucleotide polymorphisms. A subgroup of stable renal transplant recipients was identified to determine a ddcfDNA threshold value.ResultsIn stable transplant recipients, plasma ddcfDNA% decreased to a mean (SD) ddcfDNA% of 0.46% (± 0.21%) which was reached 9.85 (± 5.6) days after transplantation. A ddcfDNA threshold value of 0.88% (mean + 2SD) was determined in kidney transplant recipients. Recipients that did not reach this threshold ddcfDNA value within 10 days after transplantation showed a higher ddcfDNA% on the first day after transplantation and demonstrated a higher individual baseline ddcfDNA%.ConclusionIn conclusion, plasma ddcfDNA fractions decreased exponentially within 10 days after transplantation to a ddcfDNA threshold value of 0.88% or less. To investigate the role of ddcfDNA for rejection monitoring of the graft, future research is needed to determine causes of ddcfDNA% increases above this threshold value.