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Pre‐transplant phospholipase A2 receptor autoantibody concentration is associated with clinically significant recurrence of membranous nephropathy post‐kidney transplantation
Authors:Gaurav Gupta  Hasan Fattah  Rivka Ayalon  Jason Kidd  Todd Gehr  Luis F. Quintana  Pamela Kimball  Salima Sadruddin  H. Davis Massey  Dhiren Kumar  Anne L. King  Laurence H. Beck Jr
Affiliation:1. Division of Nephrology, Virginia Commonwealth University School of Medicine, Richmond, VA, USA;2. Division of Nephrology, Boston University School of Medicine, Boston, MA, USA;3. Servicio de Nefrología y Trasplante Renal, Hospital Clinic, Barcelona, Spain;4. Division of Transplant Surgery, Virginia Commonwealth University School of Medicine, Richmond, VA, USA;5. Department of Pathology, Virginia Commonwealth University School of Medicine, Richmond, VA, USA
Abstract:Previous studies that have assessed the association of pre‐transplant antiphospholipase A2 receptor autoantibody (PLA2R‐Ab) concentration with a recurrence of membranous nephropathy (rMN) post‐kidney transplant have yielded variable results. We tested 16 consecutive transplant patients with a history of iMN for pre‐transplant PLA2R‐Ab. Enzyme‐linked immunosorbent assay titers (Euroimmun, NJ, USA) >14 RU/mL were considered positive. A receiver operating characteristic (ROC) analysis was performed after combining data from Quintana et al. (n = 21; Transplantation February 2015) to determine a PLA2R‐Ab concentration which could predict rMN. Six of 16 (37%) patients had biopsy‐proven rMN at a median of 3.2 yr post‐transplant. Of these, five of six (83%) had a positive PLA2R‐Ab pre‐transplant with a median of 82 RU/mL (range = 31–1500). The only patient who had rMN with negative PLA2R‐Ab was later diagnosed with B‐cell lymphoma. One hundred percent (n = 10) of patients with no evidence of rMN (median follow‐up = five yr) had negative pre‐transplant PLA2R‐Ab. In a combined ROC analysis (n = 37), a pre‐transplant PLA2R‐Ab > 29 RU/mL predicted rMN with a sensitivity of 85% and a specificity of 92%. Pre‐transplant PLA2R‐Ab could be a useful tool for the prediction of rMN. Patients with rMN in the absence of PLA2R‐Ab should be screened for occult malignancy and/or alternate antigens.
Keywords:antiphospholipase A2 receptor autoantibody  idiopathic membranous nephropathy  kidney transplantation  recurrent membranous nephropathy
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