Related Experiment Video
Updated: Jan 20, 2026

'Bioluminescent' Reporter Phage for the Detection of Category A Bacterial Pathogens
Published on: July 8, 2011
Dual MPO-ANCA and PLA2R positivity in crescentic glomerulonephritis with MPO-associated membranous nephropathy: a
Chikayuki Morimoto1, Yoshihide Fujigaki2,3, Hitoshi Anzai1
1Department of Internal Medicine, Teikyo University School of Medicine, Itabashi-ku, Tokyo, Japan.
Abstract:
Recent studies have suggested that myeloperoxidase (MPO) may serve as a target antigen in cases of MPO-associated membranous nephropathy (MN) occurring concurrently with MPO-antineutrophil cytoplasmic antibody (ANCA)-associated crescentic glomerulonephritis (GN). We report the case of a 41-year-old Filipino man with MPO-ANCA-positive rapidly progressive glomerulonephritis (RPGN) complicated by the development of nephrotic syndrome. He exhibited no apparent signs of extra-renal vasculitis. Kidney biopsy demonstrated crescentic GN with MPO-associated MN, characterized by active cellular crescents and Churg stage II-III MN with positive staining for the phospholipase A2 receptor (PLA2R). Immunosuppressive therapy achieved concurrent remission of both RPGN and nephrotic syndrome, accompanied by a marked reduction in MPO-ANCA titers. This favorable response suggests that MPO-ANCA may contribute to the pathogenesis of both glomerular disease processes in this patient. Nonetheless, the possibility that the treatment was also effective against idiopathic MN cannot be excluded. The renal pathology showed early active crescentic GN without chronic changes, whereas the MN did not appear to represent an early stage. These findings suggest two possible mechanisms: first, that MPO-IgG immune complexes initially formed in MN, accompanied by bystander deposition of glomerular PLA2R, followed by the subsequent development of crescentic GN; or second, that MPO was deposited within preexisting PLA2R-positive immune complexes of idiopathic MN at the time crescentic GN emerged. Although the former mechanism appears more plausible given the increasing number of reports describing established MPO-associated MN, further studies are warranted to elucidate the pathogenic role of MPO in this condition.
Insights
Myeloperoxidase (MPO)-antineutrophil cytoplasmic antibody (ANCA)-associated glomerulonephritis (GN) and membranous nephropathy (MN) can occur together. Treatment led to remission of both conditions, suggesting MPO-ANCA
Area of Science:
- Nephrology
- Immunology
- Pathology
Background:
- Myeloperoxidase (MPO)-associated membranous nephropathy (MN) is increasingly recognized.
- Concurrent MPO-antineutrophil cytoplasmic antibody (ANCA)-associated crescentic glomerulonephritis (GN) with MN is rare.
- The role of MPO-ANCA in dual glomerular pathology requires further investigation.
Purpose of the Study:
- To report a case of MPO-ANCA-positive rapidly progressive glomerulonephritis (RPGN) with concurrent MPO-associated MN and phospholipase A2 receptor (PLA2R)-positive disease.
- To investigate the clinical course and treatment response in this complex presentation.
- To explore potential pathogenic mechanisms linking MPO-ANCA, crescentic GN, and MN.
Main Methods:
- Case report of a 41-year-old male with MPO-ANCA-positive RPGN and nephrotic syndrome.
- Renal biopsy analysis showing crescentic GN and MPO-associated MN with PLA2R staining.
- Treatment with immunosuppressive therapy and monitoring of clinical parameters and MPO-ANCA titers.
Main Results:
- The patient presented with RPGN and developed nephrotic syndrome.
- Kidney biopsy confirmed crescentic GN and MPO-associated MN (Churg stage II-III) with PLA2R positivity.
- Immunosuppressive therapy resulted in concurrent remission of RPGN and nephrotic syndrome, with decreased MPO-ANCA titers.
Conclusions:
- MPO-ANCA may play a role in the pathogenesis of both crescentic GN and MN in select patients.
- Two potential mechanisms are proposed: MPO-IgG complex formation preceding PLA2R deposition, or MPO deposition in pre-existing PLA2R-positive MN.
- Further research is needed to clarify the pathogenic role of MPO in these overlapping glomerular diseases.
More Related Videos
07:15Mechanism of Kemeng Fang's Inhibition of Podocyte Apoptosis in Rats with Membranous Nephropathy through the PI3K/AKT Signaling Pathway
Published on: August 23, 2024
09:16Supervised Machine Learning for Semi-Quantification of Extracellular DNA in Glomerulonephritis
Published on: June 18, 2020
Related Concept Videos
11:31'Bioluminescent' Reporter Phage for the Detection of Category A Bacterial Pathogens
07:15Mechanism of Kemeng Fang's Inhibition of Podocyte Apoptosis in Rats with Membranous Nephropathy through the PI3K/AKT Signaling Pathway
09:16Supervised Machine Learning for Semi-Quantification of Extracellular DNA in Glomerulonephritis
13:48Studying Membrane Biogenesis with a Luciferase-Based Reporter Gene Assay
08:07Profiling of Surface Protein Epitopes on Viral Particles by Multiplex Dual-Reporter Strategy
07:33In vivo Dual Substrate Bioluminescent Imaging