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Diagnostic application of transcripts associated with antibody-mediated rejection in kidney transplant biopsies.
Toulza, Frederic; Dominy, Kathy; Willicombe, Michelle; Beadle, Jack; Santos, Eva; Cook, H Terence; Szydlo, Richard M; McLean, Adam; Roufosse, Candice.
Afiliação
  • Toulza F; Department of Immunology and Inflammation, Imperial College, Centre for Inflammatory Disease, London, UK.
  • Dominy K; Molecular Pathology Laboratory, North West London Pathology, London, UK.
  • Willicombe M; Department of Immunology and Inflammation, Imperial College, Centre for Inflammatory Disease, London, UK.
  • Beadle J; Imperial College Renal and Transplant Centre, Imperial College Healthcare NHS Trust, London, UK.
  • Santos E; Department of Immunology and Inflammation, Imperial College, Centre for Inflammatory Disease, London, UK.
  • Cook HT; Histocompatibility and Immunogenetics, North West London Pathology, London, UK.
  • Szydlo RM; Department of Immunology and Inflammation, Imperial College, Centre for Inflammatory Disease, London, UK.
  • McLean A; Department of Immunology and Inflammation, Imperial College, London, UK.
  • Roufosse C; Imperial College Renal and Transplant Centre, Imperial College Healthcare NHS Trust, London, UK.
Nephrol Dial Transplant ; 37(8): 1576-1584, 2022 07 26.
Article em En | MEDLINE | ID: mdl-34320215
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Rim Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Nephrol Dial Transplant Assunto da revista: NEFROLOGIA / TRANSPLANTE Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Rim Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Nephrol Dial Transplant Assunto da revista: NEFROLOGIA / TRANSPLANTE Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido