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The Role of Donor-Derived Cell-Free DNA in Identification of Injury in Kidney Allografts with Antibody-Mediated Rejection and De Novo DSA

H. Zhang,1 L. Liu,1 C. Zheng,2 X. Li,1 Q. Fu,1 J. Li,1 Q. Su,1 H. Huang,1 M. Ye,2 C. Wang.1

1Organ Transplant Center, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China
2BGI-Guangzhou Medical Laboratory, BGI-Shenzhen, Guangzhou, China.

Meeting: 2018 American Transplant Congress

Abstract number: 22

Keywords: Antibodies, Kidney transplantation, Rejection, Renal injury

Session Information

Session Name: Concurrent Session: Kidney Acute Antibody Mediated Rejection

Session Type: Concurrent Session

Date: Sunday, June 3, 2018

Session Time: 2:30pm-4:00pm

 Presentation Time: 3:06pm-3:18pm

Location: Room Hall 4B

Objectives: To evaluate the capacity of donor-derived cell-free DNA (dd-cfDNA) in the identification of injury in kidney allografts with antibody-mediated rejection and de novo DSA.

Methods: Blood specimens were collected in kidney allograft recipients with either antibody-mediated rejection (AMR) or de novo DSA (dnDSA) without histological lesions. The plasma level of dd-cfDNA in recipients was measured using a panel of SNP genotyping we developed, independent of the donor blood specimens.

Results: Thirty-seven recipients were enrolled for analysis (18 AMR, 7 dnDSA and 12 controls). A significant increased level of dd-cfDNA was identified in AMR group or dnDSA group compared with control group (AMR 3.04%±2.12% vs Control 0.63%±0.18%, P<0.05; AMR 1.72%±1.41% vs Control 0.63%±0.18%, P<0.05; ANOVA P<0.01). The receiver operating characteristic area under the curve (AUC) was 0.97 (95% confidence interval [95%CI], 0.96 to 1.00) and 0.84 (95%CI, 0.65 to 1.00) respectively for the discrimination of AMR or dnDSA from the control group. Positive and negative predictive values for AMR at a cutoff of 1.0% dd-cfDNA were 94.1% and 84.6%, respectively. Positive and negative likelihood ratios for AMR at a cutoff of 1.0% dd-cfDNA were 10.7 and 0.12, respectively.

Conclusions: Donor-derived cfDNA may be used to assess allograft injury in AMR and recipients with dnDSA but no histological lesions. Donor-derived cfDNA levels <1% reflect the absence of AMR and levels >1% indicate a probability of injury in dnDSA (+) recipients.

Figure legend:

Figure 1. The plasma level of donor-derived cell-free DNA (dd-cfDNA) in antibody-mediated rejection (AMR), de novo DSA and control group. *Significant at a level of 0.05.

CITATION INFORMATION: Zhang H., Liu L., Zheng C., Li X., Fu Q., Li J., Su Q., Huang H., Ye M., Wang C. The Role of Donor-Derived Cell-Free DNA in Identification of Injury in Kidney Allografts with Antibody-Mediated Rejection and De Novo DSA Am J Transplant. 2017;17 (suppl 3).

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To cite this abstract in AMA style:

Zhang H, Liu L, Zheng C, Li X, Fu Q, Li J, Su Q, Huang H, Ye M, Wang C. The Role of Donor-Derived Cell-Free DNA in Identification of Injury in Kidney Allografts with Antibody-Mediated Rejection and De Novo DSA [abstract]. https://atcmeetingabstracts.com/abstract/the-role-of-donor-derived-cell-free-dna-in-identification-of-injury-in-kidney-allografts-with-antibody-mediated-rejection-and-de-novo-dsa/. Accessed May 16, 2025.

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