A 2020 Banff Antibody-mediatedInjury Working Group examination of international practices for diagnosing antibody-mediated rejection in kidney transplantation - a cohort study.

HLA-antibody post-transplantation histocompatibility and immunogenetics kidney clinical pre-sensitisation rejection

Journal

Transplant international : official journal of the European Society for Organ Transplantation
ISSN: 1432-2277
Titre abrégé: Transpl Int
Pays: Switzerland
ID NLM: 8908516

Informations de publication

Date de publication:
03 2021
Historique:
received: 13 11 2020
revised: 24 11 2020
accepted: 02 01 2021
pubmed: 11 1 2021
medline: 29 6 2021
entrez: 10 1 2021
Statut: ppublish

Résumé

The Banff antibody-mediated rejection (ABMR) classification is vulnerable to misinterpretation, but the reasons are unclear. To better understand this vulnerability, we evaluated how ABMR is diagnosed in practice. To do this, the Banff Antibody-Mediated Injury Workgroup electronically surveyed an international cohort of nephrologists/surgeons (n = 133) and renal pathologists (n = 99). Most providers (97%) responded that they use the Banff ABMR classification at least sometimes, but DSA information is often not readily available. Only 41.1% (55/133) of nephrologists/surgeons and 19.2% (19/99) of pathologists reported that they always have DSA results when the biopsy is available. Additionally, only 19.6% (26/133) of nephrologists/surgeons responded that non-HLA antibody or molecular transcripts are obtained when ABMR histologic features are present but DSA is undetected. Several respondents agreed that histologic features concerning for ABMR in the absence of DSA and/or C4d are not well accounted for in the current classification [31.3% (31/99) pathologists and 37.6% (50/133) nephrologist/surgeons]. The Banff ABMR classification appears widely accepted, but efforts to improve the accessibility of DSA information for the multidisciplinary care team are needed. Further clarity is also needed in Banff ABMR nomenclature to account for the spectrum of ABMR and for histologic features suspicious for ABMR when DSA is absent.

Identifiants

pubmed: 33423340
doi: 10.1111/tri.13813
doi:

Substances chimiques

Isoantibodies 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

488-498

Informations de copyright

© 2021 Steunstichting ESOT. Published by John Wiley & Sons Ltd.

Références

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Auteurs

Carrie A Schinstock (CA)

William J. von Liebig Center for Transplantation and Clinical Regeneration, Mayo Clinic, Rochester, MN, USA.

Medhat Askar (M)

Baylor University Medical Center, Dallas, TX, USA.
Texas A&M Health Science Center Collect of Medicine, Bryan, TX, USA.

Serena M Bagnasco (SM)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Ibrahim Batal (I)

Department of Pathology and Cell Biology, Columbia University Medical Center, New York, NY, USA.

Laurine Bow (L)

Department of Transplantation Surgery, Yale University School of Medicine, New Haven, CT, USA.

Klemens Budde (K)

Medizinische Klinik mit Schwerpunkt Nephrologie und Internistische Intensivmedizin, Charité Universitätsmedizin Berlin, Berlin, Germany.

Patricia Campbell (P)

Department of Medicine and Clinical Islet Transplant Program, University of Alberta, Edmonton, AB, Canada.

Robert Carroll (R)

Transplantation Immunogenetics Service, Australian Red Cross Blood Service Melbourne, Melbourne, Vic., Australia.
University of South Australia, Adelaide, SA, Australia.

Marian C Clahsen-van Groningen (MC)

Department of Pathology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.

Matthew Cooper (M)

Medstar Georgetown Transplant Institute, Washington, DC, USA.

Lynn D Cornell (LD)

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.

Emanuele Cozzi (E)

Transplant Immunology Unit, Department of Cardiac, Thoracic and Vascular Sciences, Padua University Hospital, Padua, Italy.

Darshana Dadhania (D)

Department of Medicine, Weill Cornell Medicine - New York Presbyterian Hospital, New York, NY, USA.

Fritz Diekmann (F)

Kidney Transplant Unit, Institut d'Incestigacions Biomèdiques August Pi i Sunyer, Hospital Clínic, Barcelona, Spain.

Dennis A Hesselink (DA)

Department of Nephrology and Transplantation, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.

Annette M Jackson (AM)

Department of Surgery, Duke University, Durham, NC, USA.

Zeljko Kikic (Z)

Division of Nephrology and Dialysis, Department of Medicine III, Medical University Vienna, Vienna, Austria.

Fritz Lower (F)

Department of Pathology and Laboratory Medicine, University of Kentucky, Lexington, KY, USA.

Maarten Naesens (M)

Department of Microbiology and Immunology, KU Leuven, Leuven, Belgium.
Department of Nephrology, University Hospitals Leuven, Leuven, Belgium.

Joris J Roelofs (JJ)

Department of Pathology, Amsterdam University Medical Centers, Amsterdam, The Netherlands.

Ruth Sapir-Pichhadze (R)

Centre for Outcomes Research & Evaluation Research Institute, McGill University Health Center, Montreal, QC, Canada.

Edward S Kraus (ES)

Division of Nephrology/Transplant Nephrology, Johns Hopkins University, Baltimore, MD, USA.

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