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Am J Transplant. 2019 Jan;19(1):98-109. doi: 10.1111/ajt.15011. Epub 2018 Aug 31.

Development and clinical validity of a novel blood-based molecular biomarker for subclinical acute rejection following kidney transplant.

Author information

1
Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
2
Scripps Health, La Jolla, CA, USA.
3
Mayo Clinic, Phoenix, AZ, USA.
4
UC San Diego Center for Computational Biology & Bioinformatics, San Diego, CA, USA.
5
Cleveland Clinic, Cleveland, OH, USA.
6
Medical University of South Carolina, Charleston, SC, USA.
7
National Institute of Allergy and Infectious Diseases, Bethesda, MD, USA.
8
Rho Federal Systems, Chapel Hill, NC, USA.

Abstract

Noninvasive biomarkers are needed to monitor stable patients after kidney transplant (KT), because subclinical acute rejection (subAR), currently detectable only with surveillance biopsies, can lead to chronic rejection and graft loss. We conducted a multicenter study to develop a blood-based molecular biomarker for subAR using peripheral blood paired with surveillance biopsies and strict clinical phenotyping algorithms for discovery and validation. At a predefined threshold, 72% to 75% of KT recipients achieved a negative biomarker test correlating with the absence of subAR (negative predictive value: 78%-88%), while a positive test was obtained in 25% to 28% correlating with the presence of subAR (positive predictive value: 47%-61%). The clinical phenotype and biomarker independently and statistically correlated with a composite clinical endpoint (renal function, biopsy-proved acute rejection, ≥grade 2 interstitial fibrosis, and tubular atrophy), as well as with de novo donor-specific antibodies. We also found that <50% showed histologic improvement of subAR on follow-up biopsies despite treatment and that the biomarker could predict this outcome. Our data suggest that a blood-based biomarker that reduces the need for the indiscriminate use of invasive surveillance biopsies and that correlates with transplant outcomes could be used to monitor KT recipients with stable renal function, including after treatment for subAR, potentially improving KT outcomes.

KEYWORDS:

alloantibody; biomarker; clinical research/practice; clinical trial; genomics; kidney transplantation/nephrology; rejection: subclinical; translational research/science

PMID:
29985559
DOI:
10.1111/ajt.15011

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