The use of plasma donor-derived, cell-free DNA to monitor acute rejection after kidney transplantation

Author:

Gielis Els M1,Ledeganck Kristien J1,Dendooven Amélie2,Meysman Pieter34,Beirnaert Charlie34,Laukens Kris34,De Schrijver Joachim5,Van Laecke Steven6,Van Biesen Wim6,Emonds Marie-Paule7,De Winter Benedicte Y1,Bosmans Jean-Louis18,Del Favero Jurgen5,Abramowicz Daniel18

Affiliation:

1. Laboratory of Experimental Medicine and Pediatrics, University of Antwerp, Antwerp, Belgium

2. Department of Pathology, Antwerp University Hospital, Antwerp, Belgium

3. Biomedical Informatics Research Network Antwerp (Biomina), University of Antwerp/Antwerp University Hospital, Antwerp, Belgium

4. Advanced Database Research and Modelling (ADReM), Department of Mathematics and Computer Science, University of Antwerp, Antwerp, Belgium

5. Multiplicom N.V., part of Agilent Technologies, Niel, Belgium

6. Department of Nephrology, Renal Division, Ghent University Hospital, Ghent, Belgium

7. Histocompatibility and Immunogenetic Laboratory, Belgian Red Cross Flanders, Mechelen, Belgium

8. Department of Nephrology and Hypertension, Antwerp University Hospital, Antwerp, Belgium

Abstract

Abstract Background After transplantation, cell-free deoxyribonucleic acid (DNA) derived from the donor organ (ddcfDNA) can be detected in the recipient’s circulation. We aimed to investigate the role of plasma ddcfDNA as biomarker for acute kidney rejection. Methods From 107 kidney transplant recipients, plasma samples were collected longitudinally after transplantation (Day 1 to 3 months) within a multicentre 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 polymerase chain reaction-based method for the analysis of single nucleotide polymorphisms. Results Increases of the ddcfDNA% above a threshold value of 0.88% were significantly associated with the occurrence of episodes of acute rejection (P = 0.017), acute tubular necrosis (P = 0.011) and acute pyelonephritis (P = 0.032). A receiver operating characteristic curve analysis revealed an equal area under the curve of the ddcfDNA% and serum creatinine of 0.64 for the diagnosis of acute rejection. Conclusions Although increases in plasma ddcfDNA% are associated with graft injury, plasma ddcfDNA does not outperform the diagnostic capacity of the serum creatinine in the diagnosis of acute rejection.

Funder

Flanders Innovation and Entrepreneurship

Fellowship of the Research Foundation–Flanders

FWO

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

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