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Donor-Derived Cell-Free DNA as a Biomarker of T Cell Mediated Rejection in Pediatric Kidney Transplant Patients

R. Dandamudi1, S. Federman2, R. Woodward2, S. Dholakia2, L. Walther1, V. Dharnidharka1

1Pediatrics, Washington University School of Medicine in St. Louis, St. Louis, MO, 2CareDx, Brisbane, CA

Meeting: 2022 American Transplant Congress

Abstract number: 111

Keywords: Kidney transplantation, Pediatric

Topic: Clinical Science » Kidney » 43 - Kidney: Pediatrics

Session Information

Session Name: Kidney: Pediatrics

Session Type: Rapid Fire Oral Abstract

Date: Sunday, June 5, 2022

Session Time: 5:30pm-7:00pm

 Presentation Time: 6:40pm-6:50pm

Location: Hynes Ballroom C

*Purpose: T-cell-mediated rejection (TCMR) is a major cause of kidney allograft failure which requires kidney biopsy for a definitive diagnosis. Donor-derived cell-free DNA (dd-cfDNA) is an emerging biomarker used to assess kidney allograft injury, with scant pediatric data. This study was conducted to investigate the accuracy of dd-cfDNA as a non-invasive marker of TCMR in a pediatric kidney transplant population.

*Methods: In this retrospective single-center observational study, we studied 63 patients who had concurrent 123 dd-cfDNA levels along with kidney biopsies within the first year post-transplant that showed either TCMR or normal, all other pathologies were excluded and we had no ABMR before month 12. We included both surveillance biopsies (3, 6 and 12 months) and diagnostic biopsies. We quantified dd-cfDNA 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 (AlloSure, CareDx, Brisbane, CA). Treating each sample as independent, we divided the 123 biopsy samples with concurrent dd-CFDNA levels into two groups (no evidence of TCMR vs Any TCMR, including subclinical rejection) and analyzed the data.

*Results: The median (IQR) of dd-cfDNA in TCMR group(n=30) of 0.55% (0.29-1.18%) was significantly higher than 0.21% (0.13-0.46 %) in non-TCMR (n= (93) (p < 0.001; Figure) by Mann-Whitney U test. The area under the curve was 0.73 (95% CI, 0.62 to 0.84: Figure). With a cutoff of 1.0%, dd-cfDNA had a 95.7% specificity (95% CI, 89.5% to 98.3%) and 30% sensitivity (95% CI, 16.7% to 47.9%) to discriminate TCMR from no rejection. With a cutoff of 0.5%, dd-cfDNA had a 80% specificity (95% CI, 71.5 to 87.4) and 56.7% sensitivity (95% CI, 39.2% to 72.62%) to discriminate TCMR from no rejection.

*Conclusions: Our data show that pediatric patients have a similar high AUC and specificity to the 0.74 AUC and 83% specificity shown in the adult DART study (Bloom et al, JASN 2017). But the sensitivity in children was lower than the 81% in DART, perhaps related to allograft size mismatch that may elevate some dd-cfDNA levels without injury

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To cite this abstract in AMA style:

Dandamudi R, Federman S, Woodward R, Dholakia S, Walther L, Dharnidharka V. Donor-Derived Cell-Free DNA as a Biomarker of T Cell Mediated Rejection in Pediatric Kidney Transplant Patients [abstract]. Am J Transplant. 2022; 22 (suppl 3). https://atcmeetingabstracts.com/abstract/donor-derived-cell-free-dna-as-a-biomarker-of-t-cell-mediated-rejection-in-pediatric-kidney-transplant-patients/. Accessed May 17, 2025.

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