Abstract

Membranous nephropathy (MN) is the leading cause of nephrotic syndrome in adults. We previously reported that the prevalence of phospholipase A2 receptor (PLA2R)- and thrombospondin type 1 domain containing 7A (THSD7A)-associated MN patients in Japan is 52.7% and 9.1%, respectively. In addition to PLA2R and THSD7A, we assessed the presence of newly discovered target antigens, neural epidermal growth factor-like 1 (NELL-1), semaphorin 3B (SEMA3B), and exostosin 1/exostosin 2 (Ext1/Ext2), in renal specimens from patients with primary and secondary MN by immunohistochemistry. We found enhanced glomerular staining of PLA2R, THSD7A, NELL-1, and Ext1/Ext2 in 53.6%, 8.7%, 1.5%, and 13.0% of the renal samples, respectively, in patients with primary MN. None of the patient specimens showed enhanced staining of SEMA3B. Enhanced glomerular staining of PLA2R, NELL-1, and Ext1/Ext2 was detected in 5.7%, 8.6%, and 22.9% of the patients with secondary MN, respectively. Based on our findings, we recommend the assessment of PLA2R, THSD7A and NELL-1 in addition to clinical information and IgG4 staining to differentiate between primary and secondary MN. This would aid in distinguishing secondary MN patients from primary MN patients who coincidentally have some secondary characteristics.

Highlights

  • Membranous nephropathy (MN) is the leading cause of nephrotic syndrome in adults

  • Renal immunohistochemical assessment of corresponding antigens identifies MN patients with autoantibodies, as the presence of serum autoantibodies against phospholipase A2 receptor (PLA2R)/THSD7A/ neural epidermal growth factor-like 1 (NELL-1)/semaphorin 3B (SEMA3B) antigens enhance the antigens staining along G­ BM5,12,14,16,18,19

  • Five patients were infected with hepatitis B virus (HBV)

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Summary

Introduction

Membranous nephropathy (MN) is the leading cause of nephrotic syndrome in adults. We previously reported that the prevalence of phospholipase A2 receptor (PLA2R)- and thrombospondin type 1 domain containing 7A (THSD7A)-associated MN patients in Japan is 52.7% and 9.1%, respectively. In addition to PLA2R and THSD7A, we assessed the presence of newly discovered target antigens, neural epidermal growth factor-like 1 (NELL-1), semaphorin 3B (SEMA3B), and exostosin 1/exostosin 2 (Ext1/ Ext2), in renal specimens from patients with primary and secondary MN by immunohistochemistry. We found enhanced glomerular staining of PLA2R, THSD7A, NELL-1, and Ext1/Ext[2] in 53.6%, 8.7%, 1.5%, and 13.0% of the renal samples, respectively, in patients with primary MN. Enhanced glomerular staining of PLA2R, NELL-1, and Ext1/Ext[2] was detected in 5.7%, 8.6%, and 22.9% of the patients with secondary MN, respectively. Renal immunohistochemical assessment of corresponding antigens identifies MN patients with autoantibodies, as the presence of serum autoantibodies against PLA2R/THSD7A/ NELL-1/SEMA3B antigens enhance the antigens staining along G­ BM5,12,14,16,18,19. We are extending our previous ­study[22], and aim to demonstrate the detection rate of the target antigens in primary MN

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