Diagnostic application of transcripts associated with antibody-mediated rejection in kidney transplant biopsies

Author:

Toulza Frederic1ORCID,Dominy Kathy2,Willicombe Michelle13,Beadle Jack1,Santos Eva4,Cook H Terence1,Szydlo Richard M5,McLean Adam3,Roufosse Candice1

Affiliation:

1. Department of Immunology and Inflammation, Imperial College, Centre for Inflammatory Disease, London, UK

2. Molecular Pathology Laboratory, North West London Pathology, London, UK

3. Imperial College Renal and Transplant Centre, Imperial College Healthcare NHS Trust, London, UK

4. Histocompatibility and Immunogenetics, North West London Pathology, London, UK

5. Department of Immunology and Inflammation, Imperial College, London, UK

Abstract

Abstract Background The diagnosis of antibody-mediated rejection (AMR) is reached using the Banff Classification for Allograft Pathology, which now includes gene expression analysis. In this study, we investigate the application of ‘increased expression of thoroughly validated gene transcripts/classifiers strongly associated with AMR’ as diagnostic criteria. Method We used quantitative real-time polymerase chain reaction for 10 genes associated with AMR in a retrospective cohort of 297 transplant biopsies, including biopsies that met the full diagnostic criteria for AMR, even without molecular data (AMR, n = 27), biopsies that showed features of AMR, but that would only meet criteria for AMR with increased transcripts [suspicious for AMR (AMRsusp), n = 49] and biopsies that would never meet criteria for AMR (No-AMR, n = 221). Results A 10-gene AMR score trained by a receiver-operating characteristic to identify AMR found 16 cases with a high score among the AMRsusp cases (AMRsusp-high) that had significantly worse graft survival than those with a low score (AMRsusp-low; n = 33). In both univariate and multivariate Cox regression analysis, the AMR 10-gene score was significantly associated with an increased hazard ratio (HR) for graft loss (GL) in the AMRsusp group (HR = 1.109, P = 0.004 and HR = 1.138, P = 0.012, respectively), but not in the whole cohort. Net reclassification index and integrated discrimination improvement analyses demonstrated improved risk classification and superior discrimination, respectively, for GL when considering the gene score in addition to histological and serological data, but only in the AMRsusp group, not the whole cohort. Conclusions This study provides evidence that a gene score strongly associated with AMR helps identify cases at higher risk of GL in biopsies that are suspicious for AMR but do not meet full criteria.

Funder

National Institute for Health Research (NIHR) Biomedical Research Centre based at Imperial College Healthcare NHS Trust and Imperial College London

NIHR Imperial Biomedical Research Centre

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

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