Donor-Specific Antibody Is Associated with Increased Expression of Rejection Transcripts in Renal Transplant Biopsies Classified as No Rejection
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
34253587
PubMed Central
PMC8806080
DOI
10.1681/asn.2021040433
PII: 00001751-202111000-00013
Knihovny.cz E-zdroje
- Klíčová slova
- gene expression, kidney biopsy, rejection, renal transplantation, transplantation,
- MeSH
- analýza hlavních komponent MeSH
- analýza přežití MeSH
- biopsie MeSH
- čipová analýza tkání MeSH
- dárci tkání * MeSH
- exprese genu MeSH
- falešně negativní reakce MeSH
- genetická transkripce MeSH
- HLA antigeny imunologie MeSH
- isoprotilátky imunologie MeSH
- ledviny patologie MeSH
- přežívání štěpu MeSH
- prospektivní studie MeSH
- rejekce štěpu genetika MeSH
- specificita protilátek MeSH
- transplantace ledvin * MeSH
- transplantáty patologie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- HLA antigeny MeSH
- isoprotilátky MeSH
BACKGROUND: Donor -specific HLA antibody (DSA) is present in many kidney transplant patients whose biopsies are classified as no rejection (NR). We explored whether in some NR kidneys DSA has subtle effects not currently being recognized. METHODS: We used microarrays to examine the relationship between standard-of-care DSA and rejection-related transcript increases in 1679 kidney transplant indication biopsies in the INTERCOMEX study (ClinicalTrials.gov NCT01299168), focusing on biopsies classified as NR by automatically assigned archetypal clustering. DSA testing results were available for 835 NR biopsies and were positive in 271 (32%). RESULTS: DSA positivity in NR biopsies was associated with mildly increased expression of antibody-mediated rejection (ABMR)-related transcripts, particularly IFNG-inducible and NK cell transcripts. We developed a machine learning DSA probability (DSAProb) classifier based on transcript expression in biopsies from DSA-positive versus DSA-negative patients, assigning scores using 10-fold cross-validation. This DSAProb classifier was very similar to a previously described "ABMR probability" classifier trained on histologic ABMR in transcript associations and prediction of molecular or histologic ABMR. Plotting the biopsies using Uniform Manifold Approximation and Projection revealed a gradient of increasing molecular ABMR-like transcript expression in NR biopsies, associated with increased DSA (P<2 × 10-16). In biopsies with no molecular or histologic rejection, increased DSAProb or ABMR probability scores were associated with increased risk of kidney failure over 3 years. CONCLUSIONS: Many biopsies currently considered to have no molecular or histologic rejection have mild increases in expression of ABMR-related transcripts, associated with increasing frequency of DSA. Thus, mild molecular ABMR-related pathology is more common than previously realized.
Alberta Transplant Applied Genomics Centre Edmonton Alberta Canada
Department of Nephrology Hannover Medical School Hannover Germany
Department of Pathology Medical University of Warsaw Warsaw Poland
Department of Surgery University of Wisconsin Madison Wisconsin
Departments of Surgery and Microbiology and Immunology University of Maryland Baltimore Maryland
Division of Nephrology Virginia Commonwealth University Richmond Virginia
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ClinicalTrials.gov
NCT01299168