Institut Català de la Salut
[Sethi S] Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA. [Beck LH] Section of Nephrology, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA. [Glassock RJ] Department of Medicine, Geffen School of Medicine at UCLA, University of California, Los Angeles, Los Angeles, California, USA. [Haas M] Department of Pathology & Laboratory Medicine, Cedars-Sinai Medical Center, Los Angeles, California, USA. [De Vriese AS] Division of Nephrology and Infectious Diseases, AZ Sint-Jan Brugge, Brugge, Belgium. Department of Internal Medicine, Ghent University, Ghent, Belgium. [Caza TN] Arkana Laboratories, Little Rock, Arkansas, USA. [Soler MJ] Servei de Nefrologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Centro de Referencia en Enfermedad, Glomerular Compleja del Sistema Nacional de Salud de España (CSUR), Barcelona, Spain
Vall d'Hebron Barcelona Hospital Campus
2023-11-23T10:32:44Z
2023-11-23T10:32:44Z
2023-11
Consensus; Membranous nephropathy
Consens; Nefropatia membranosa
Consenso; Nefropatía membranosa
Membranous nephropathy (MN) is a pattern of injury caused by autoantibodies binding to specific target antigens, with accumulation of immune complexes along the subepithelial region of glomerular basement membranes. The past 20 years have brought revolutionary advances in the understanding of MN, particularly via the discovery of novel target antigens and their respective autoantibodies. These discoveries have challenged the traditional classification of MN into primary and secondary forms. At least 14 target antigens have been identified, accounting for 80%–90% of cases of MN. Many of the forms of MN associated with these novel MN target antigens have distinctive clinical and pathologic phenotypes. The Mayo Clinic consensus report on MN proposes a 2-step classification of MN. The first step, when possible, is identification of the target antigen, based on a multistep algorithm and using a combination of serology, staining of the kidney biopsy tissue by immunofluorescence or immunohistochemistry, and/or mass spectrometry methodology. The second step is the search for a potential underlying disease or associated condition, which is particularly relevant when knowledge of the target antigen is available to direct it. The meeting acknowledges that the resources and equipment required to perform the proposed testing may not be generally available. However, the meeting consensus was that the time has come to adopt an antigen-based classification of MN because this approach will allow for accurate and specific MN diagnosis, with significant implications for patient management and targeted treatment.
Article
Published version
English
Autoanticossos; Glomerulonefritis - Diagnòstic; Decisió de grup; DISEASES::Immune System Diseases::Autoimmune Diseases::Glomerulonephritis, Membranous; PSYCHIATRY AND PSYCHOLOGY::Behavior and Behavior Mechanisms::Psychology, Social::Group Processes::Consensus; CHEMICALS AND DRUGS::Amino Acids, Peptides, and Proteins::Proteins::Blood Proteins::Immunoproteins::Immunoglobulins::Antibodies::Autoantibodies; ENFERMEDADES::enfermedades del sistema inmune::enfermedades autoinmunes::glomerulonefritis membranosa; PSIQUIATRÍA Y PSICOLOGÍA::conducta y mecanismos de la conducta::psicología social::procesos de grupo::consenso; COMPUESTOS QUÍMICOS Y DROGAS::aminoácidos, péptidos y proteínas::proteínas::proteínas sanguíneas::inmunoproteínas::inmunoglobulinas::anticuerpos::autoanticuerpos
Elsevier
Mayo Clinic Proceedings;98(11)
https://doi.org/10.1016/j.mayocp.2023.08.006
Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
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