Frontiers in Transplantation (Dec 2024)

Donor-derived cell-free DNA in chronic lung allograft dysfunction phenotypes: a pilot study

  • H. Beeckmans,
  • A. Pagliazzi,
  • P. Kerckhof,
  • R. Hofkens,
  • F. Debackere,
  • A. Zajacova,
  • S. Bos,
  • S. Bos,
  • B. M. Vanaudenaerde,
  • H. de Loor,
  • M. Naesens,
  • M. Naesens,
  • R. Vos,
  • R. Vos

DOI
https://doi.org/10.3389/frtra.2024.1513101
Journal volume & issue
Vol. 3

Abstract

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Long-term survival after lung transplantation is limited due to chronic lung allograft dysfunction (CLAD), which encompasses two main phenotypes: bronchiolitis obliterans syndrome (BOS) and restrictive allograft syndrome (RAS). Donor-derived cell-free DNA (dd-cfDNA) is a biomarker for (sub)clinical allograft injury and could be a tool for monitoring of lung allograft health across the (pre)clinical spectrum of CLAD. In this proof-of-concept study, we therefore assessed post-transplant plasma dd-cfDNA levels in 20 CLAD patients (11 BOS and 9 RAS) at three consecutive time points free from concurrent infection or acute rejection, during stable condition, preclinical CLAD, and established CLAD (n = 3 × 20 samples). Elevated dd-cfDNA levels were detected in 47% of stable samples, in 66% of preclinical CLAD samples, and in 71% of CLAD samples, indicating ongoing allograft injury. However, dd-cfDNA levels exhibited high intra- and interpatient variability and did not significantly differ between BOS and RAS (p = 0.25), although the range of dd-cfDNA was higher in RAS. Dd-cfDNA detects ongoing allograft injury in patients with CLAD, which warrants further investigation to improve early detection of CLAD.

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