Literature DB >> 26418703

Graft-Derived Cell-Free DNA as a Marker of Transplant Graft Injury.

Michael Oellerich1, Philip D Walson, Julia Beck, Jessica Schmitz, Otto Kollmar, Ekkehard Schütz.   

Abstract

Although short-term success after solid organ transplantation is good, long-term graft and recipient survival are both not satisfactory. Despite therapeutic drug monitoring (TDM) of immunosuppressive drugs (ISDs), both excessive and insufficient immunosuppression still do occur. There is a need for new biomarkers that, when combined with TDM, can be used to provide more effective and less toxic, personalized immunosuppression to improve long-term survival. Currently used methods are insufficient to rapidly, cost-effectively, and directly interrogate graft integrity after solid organ transplantation. However, because organ transplants are also genome transplants, measurement of graft-derived circulating cell-free DNA (GcfDNA) has shown promise as a way to improve both graft and recipient outcomes after solid organ transplantation through the early detection of severe graft injury, enabling an early intervention. A newly developed droplet digital polymerase chain reaction (ddPCR) method has advantages over expensive high-throughput sequencing methods to rapidly quantify GcfDNA percentages and absolute amounts. This procedure does not require donor DNA and therefore can be applied to any organ donor/recipient pair. The droplet digital polymerase chain reaction method allows for the early, sensitive, specific, and cost-effective direct assessment of graft integrity and can be used to define individual responses to ISDs including the minimal ISD exposures necessary to prevent rejection. This is especially important in patients undergoing ISD switches due to ISD toxicity, infections, or malignancies. Although prospective, multicenter clinical trials in liver, heart, and kidney transplantation have not been completed, early results suggest that GcfDNA can be combined with TDM to guide changes in immunosuppression to provide more effective, and less toxic treatment. Personalized immunosuppression will shift emphasis in transplantation from reaction to prevention and could improve outcome at lower health care costs.

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Year:  2016        PMID: 26418703     DOI: 10.1097/FTD.0000000000000239

Source DB:  PubMed          Journal:  Ther Drug Monit        ISSN: 0163-4356            Impact factor:   3.681


  6 in total

1.  Graft-derived cell-free DNA, a noninvasive early rejection and graft damage marker in liver transplantation: A prospective, observational, multicenter cohort study.

Authors:  Ekkehard Schütz; Anna Fischer; Julia Beck; Markus Harden; Martina Koch; Tilo Wuensch; Martin Stockmann; Björn Nashan; Otto Kollmar; Johannes Matthaei; Philipp Kanzow; Philip D Walson; Jürgen Brockmöller; Michael Oellerich
Journal:  PLoS Med       Date:  2017-04-25       Impact factor: 11.069

2.  Analytical Validation of a Single-nucleotide Polymorphism-based Donor-derived Cell-free DNA Assay for Detecting Rejection in Kidney Transplant Patients.

Authors:  Yücel Altuğ; Nathan Liang; Rosalyn Ram; Harini Ravi; Ebad Ahmed; Maxim Brevnov; Ryan K Swenerton; Bernhard Zimmermann; Meenakshi Malhotra; Zachary P Demko; Paul R Billings; Allison Ryan
Journal:  Transplantation       Date:  2019-12       Impact factor: 4.939

Review 3.  Necroptosis in acute kidney injury: a shedding light.

Authors:  S Wang; C Zhang; L Hu; C Yang
Journal:  Cell Death Dis       Date:  2016-03-03       Impact factor: 8.469

4.  Cell-free DNA from human plasma and serum differs in content of telomeric sequences and its ability to promote immune response.

Authors:  Alzbeta Zinkova; Iva Brynychova; Alexander Svacina; Marie Jirkovska; Marie Korabecna
Journal:  Sci Rep       Date:  2017-06-01       Impact factor: 4.379

5.  Quantitative PCR of INDELs to measure donor-derived cell-free DNA-a potential method to detect acute rejection in kidney transplantation: a pilot study.

Authors:  Eva-Maria Dauber; Dagmar Kollmann; Nicolas Kozakowski; Susanne Rasoul-Rockenschaub; Thomas Soliman; Gabriela A Berlakovich; Wolfgang R Mayr
Journal:  Transpl Int       Date:  2019-12-13       Impact factor: 3.782

6.  Whole genome sequencing of low input circulating cell-free DNA obtained from normal human subjects.

Authors:  Julie F Foley; Brian Elgart; B Alex Merrick; Dhiral P Phadke; Molly E Cook; Jason A Malphurs; Gregory G Solomon; Ruchir R Shah; Michael B Fessler; Frederick W Miller; Kevin E Gerrish
Journal:  Physiol Rep       Date:  2021-08
  6 in total

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