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Published on: June 18, 2020
Immunopathologic co-localization of MPO, IgG, and C3 in glomeruli in human MPO-ANCA-associated glomerulonephritis
Soko Kawashima1, Yoshihiro Arimura, Katsuko Sano
1First Department of Internal Medicine, Kyorin University School of Medicine, Tokyo, Japan. sohko@ks.kyorin-u.ac.jp
Abstract:
Myeloperoxidase anti-neutrophil cytoplasmic antibody (MPO-ANCA)- associated glomerulonephritis (GN) is characterized by pauci-immune necrotizing glomerulonephritis(NGN). Although it has been thought that MPO-ANCA is involved in the pathogenesis of capillary injuries in NGN via activation of neutrophils, recent studies suggest a possible role of other factors such as immunoglobulins precipitated on the glomeruli. Here we performed a pathological study investigating a relationship of deposition of MPO, IgG, complements with regard to MPO-positive cells and glomerular capillaries in human MPO-ANCA-associated GN. Renal specimen including 317 glomeruli obtained from 20 patients with MPOANCA- associated GN were analyzed. All of the specimens showed significant focal segmental deposition of IgG. There was a significant glomerular infiltration of MPO-positive cells along with deposition of extracellular MPO in the active lesions of segmental and global NCG, with CD34 staining being decreased in the adjacent areas. IgG deposits were almost colocalized with C3 and partly with MPO, which are also associated with a decrease in CD34 staining, suggesting that immune complex formation and the resultant capillary injuries. Actually occurred, the colocalization of MPO, IgG and C3 was seen only in the glomerular lesions with low severity and activity. These results suggest that not only MPO itself released from the neutrophils but also immune complexes composed of MPO and anti-MPO antibody may play some pathogenetic roles for the glomerular injuries especially in the early phase of human MPO-ANCA-associated GN.
Insights
Myeloperoxidase anti-neutrophil cytoplasmic antibody (MPO-ANCA)-associated glomerulonephritis involves glomerular deposition of MPO and IgG. Immune complexes, not just MPO, may contribute to early kidney injury in this condition.
Area of Science:
- Nephrology
- Immunopathology
- Pathology
Background:
- Pauci-immune necrotizing glomerulonephritis (NGN) is typical in MPO-ANCA-associated GN.
- Neutrophil activation by MPO-ANCA was considered the primary cause of capillary injury.
- Emerging evidence suggests a role for glomerular-deposited immunoglobulins.
Purpose of the Study:
- To investigate the relationship between MPO, IgG, and complement deposition in MPO-ANCA-associated GN.
- To correlate these depositions with MPO-positive cells and glomerular capillary damage.
- To elucidate the pathogenetic roles of MPO and immune complexes in human MPO-ANCA-associated GN.
Main Methods:
- Pathological analysis of renal specimens from 20 patients with MPO-ANCA-associated GN.
- Examination of 317 glomeruli for MPO, IgG, and complement deposition.
- Assessment of MPO-positive cells, glomerular capillaries (CD34 staining), and lesion severity.
Main Results:
- Significant focal segmental deposition of IgG was observed in all specimens.
- Glomerular infiltration of MPO-positive cells and extracellular MPO deposition occurred in active NGN lesions.
- IgG deposits colocalized with C3 and partly with MPO, correlating with decreased CD34 staining and suggesting immune complex formation and capillary injury.
Conclusions:
- Both MPO released from neutrophils and MPO-IgG immune complexes may contribute to glomerular injury.
- These pathogenetic roles are particularly relevant in the early phase of human MPO-ANCA-associated GN.
- Findings highlight the complex interplay of immune factors in MPO-ANCA-associated GN pathogenesis.

