# Discovery of Donor-Derived Exosomal DNA as an Exploratory Biomarker of Kidney Graft Rejection: A Cross-Sectional Study

**Authors:** Elena Cuadrado-Payán, María José Ramírez-Bajo, Elisenda Banón-Maneus, Jordi Rovira, Natalia Hierro, Daniel Serrano-Jorcano, María Argudo, Enrique Montagud-Marrahi, Diana Rodríguez-Espinosa, Carolt Arana, Alicia Molina-Andújar, Angela González-Rojas, Nuria Esforzado, Vicens Torregrosa, Pedro Ventura-Aguiar, José Jesús Broseta, Eva González-Roca, Eduard Palou, Fritz Diekmann, David Cucchiari, Ignacio Revuelta

PMC · DOI: 10.3389/ti.2026.16061 · Transplant International · 2026-03-18

## TL;DR

This study explores donor-derived exosomal DNA as a potential biomarker for kidney transplant rejection, finding higher levels in rejection cases.

## Contribution

The study introduces donor-derived exosomal DNA as a novel biomarker for kidney graft rejection, distinct from cell-free DNA.

## Key findings

- Donor-derived exosomal DNA levels were significantly higher in rejection cases compared to non-rejection cases.
- Higher dd-exoDNA levels were associated with specific histological features of rejection.
- Multivariate analysis confirmed an independent association between dd-exoDNA and rejection.

## Abstract

Circulating donor DNA has emerged as a valuable tool for clinical decision-making in kidney transplantation. While most studies focus on cell-free DNA, the role of donor DNA associated with extracellular vesicles (EVs) remains unexplored. To address this, we analyzed donor-derived exosomal DNA (dd-exoDNA) in 100 kidney transplant recipients (KTR) undergoing surveillance or indicated biopsies. Serum exosomes were isolated using precipitation-based technology, and dd-exoDNA was analyzed via digital PCR targeting donor/recipient HLA-DRB1 mismatches. Dd-exoDNA levels were higher in rejection versus non-rejection (2.66 [0.56–7.10] ×10−3 vs. 0.69 [0.28–1.71] ×10−3, p = 0.004) and were associated with Banff score items: glomerulitis ≥1 (p = 0.037), peritubular capillaritis ≥1 (p = 0.040), and tubulitis ≥2 (p = 0.043). In multivariate analysis, dd-exoDNA remained independently associated with rejection, although with wide confidence intervals (OR [95%CI] 3.68 [1.32–10.26], P = 0.013). Exploratory threshold analyses suggested moderate discriminative performance. These findings indicate that donor DNA associated with circulating EVs may offer complementary information to existing biomarkers, warranting validation in external cohorts and comparison with established assays.

Infographic illustrating a study on donor-derived exosomal DNA as a kidney graft rejection biomarker, depicting sample workflow, equations, patient distribution, two scatter plots comparing DNA levels in rejection versus no rejection, and a concluding statement on biomarker detectability and clinical utility.

## Full-text entities

- **Genes:** HLA-DRB1 (major histocompatibility complex, class II, DR beta 1) [NCBI Gene 3123] {aka DRB1, HLA-DR1B, HLA-DRB, SS1}
- **Diseases:** tubulitis (MESH:D007673)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13038620/full.md

## References

52 references — full list in the complete paper: https://tomesphere.com/paper/PMC13038620/full.md

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Source: https://tomesphere.com/paper/PMC13038620