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Published on: April 19, 2017
Detection of Kidney Allograft Rejection Using Urinary Chemokines
Valentin Goutaudier1,2, Olivier Aubert3, Maud Racapé1
1Paris-Cardiovascular Research Center (PARCC) INSERM U970, Paris Institute for Transplantation and Organ Regeneration (PITOR), Université Paris Cité, Paris, France.
Urinary CXCL9 showed limited use, and urinary CXCL10 offered no added benefit for detecting kidney transplant rejection beyond standard monitoring. Further research is needed to assess their clinical utility in patient care.
Area of Science:
- Nephrology
- Transplantation Immunology
- Biomarker Discovery
Background:
- Urinary chemokines CXCL9 and CXCL10 are potential biomarkers for kidney allograft rejection.
- Their added value over standard monitoring protocols requires further investigation.
Purpose of the Study:
- To evaluate the clinical utility of urinary CXCL9 and CXCL10 in detecting kidney allograft rejection.
- To determine if these chemokines provide additional diagnostic value beyond current standard of care monitoring.
Main Methods:
- Prospective enrollment of 733 kidney transplant recipients across 7 centers.
- Quantification of urinary CXCL9 and CXCL10 via immunoassay at the time of biopsy.
- Allograft rejection classified using the Banff 2019 criteria.
Main Results:
- Urinary CXCL9 and CXCL10 showed moderate performance (AUROC 0.70 and 0.64) for rejection detection.
- Adding CXCL9 to standard models improved discrimination but not overall fit.
- CXCL10 provided no additional value; sensitivity analyses confirmed limited utility.
Conclusions:
- Urinary CXCL9 has limited clinical utility for detecting kidney allograft rejection.
- Urinary CXCL10 does not offer additional value beyond standard monitoring in the first year post-transplant.
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