Néphrologie

Primary membranous nephropathy

Primary membranous nephropathy (pMN) is an autoimmune kidney disease that is characterised by the deposition of immune complexes on the basement membrane of the glomeruli. The best-known associated autoantibodies target the phospholipase A2 receptor (PLA2R) and thrombospondin type 1 domain containing 7A (THSD7A). In recent years, a large number of new potential markers have been identified in pMN patients, including antibodies against the neural epidermal growth factor-like 1 (NELL1) glycoprotein. In a study by Sethi et al. from 2020, anti-NELL1 antibodies were detected in the renal glomeruli of 16 % of pMN patients. 

Euroimmun offers two immunofluorescence assays for the detection of anti-NELL1 antibodies for research use. The Anti-NELL1 IIFT uses cells transfected with NELL1 antigen. In addition to NELL1-transfected cells, the Membranous Nephropathy Mosaic 2 also contains BIOCHIPs with PLA2R- and THSD7A-transfected cells.