Publication

The Banff 2019 Kidney Meeting Report (I): Updates on and clarification of criteria for T cell– and antibody-mediated rejection

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Last modified
  • 05/15/2025
Type of Material
Authors
    Alexandre Loupy, Paris-Centre de Recherche CardiovasculaireMark Haas, Cedars-Sinai Medical CenterCandice Roufosse, Imperial College LondonAlton Farris III, Emory UniversityKim Solez, University of AlbertaRobert B. Colvin, Harvard Medical SchoolMichael Mengel, University of Alberta
Language
  • English
Date
  • 2020-09-01
Publisher
  • Wiley
Publication Version
Copyright Statement
  • © 2020 The Authors. American Journal of Transplantation published by Wiley Periodicals LLC on behalf of The American Society of Transplantation and the American Society of Transplant Surgeons
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 20
Issue
  • 9
Start Page
  • 2318
End Page
  • 2331
Grant/Funding Information
  • The 2019 Banff meeting received sponsorship from: CareDx, CSL Behring, Elsevier, Eppendorf, GenDx, Hansa Biopharma, Histogenetics, Immucor, Omion, OneLambda, NanoString, Novartis, Takeda, Veloxis, and Vitaeris.
Abstract
  • The XV. Banff conference for allograft pathology was held in conjunction with the annual meeting of the American Society for Histocompatibility and Immunogenetics in Pittsburgh, PA (USA) and focused on refining recent updates to the classification, advances from the Banff working groups, and standardization of molecular diagnostics. This report on kidney transplant pathology details clarifications and refinements to the criteria for chronic active (CA) T cell–mediated rejection (TCMR), borderline, and antibody-mediated rejection (ABMR). The main focus of kidney sessions was on how to address biopsies meeting criteria for CA TCMR plus borderline or acute TCMR. Recent studies on the clinical impact of borderline infiltrates were also presented to clarify whether the threshold for interstitial inflammation in diagnosis of borderline should be i0 or i1. Sessions on ABMR focused on biopsies showing microvascular inflammation in the absence of C4d staining or detectable donor-specific antibodies; the potential value of molecular diagnostics in such cases and recommendations for use of the latter in the setting of solid organ transplantation are presented in the accompanying meeting report. Finally, several speakers discussed the capabilities of artificial intelligence and the potential for use of machine learning algorithms in diagnosis and personalized therapeutics in solid organ transplantation.
Author Notes
  • See publication for full list of authors and contributors.
Keywords
Research Categories
  • Health Sciences, Pathology
  • Health Sciences, Medicine and Surgery

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