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During the congress, E-Posters will be accessible to all participants on the congress website 24/7, as well as in the E-poster stations in the congress center.
Preparing your E-Poster
Please review the E-Poster format requirements carefully when preparing your E-Poster. Should your E-Poster not meet the mentioned requirements, it may not be displayed as described above.
E-Poster Submission Deadline
Please prepare and upload your E-Poster no later than March 14, 2026 11.59PM CET. After this date, you will no longer be able to prepare and upload your E-poster and it will not be displayed and accessible on the congress website.
Please follow the instructions below to input your abstract title.
Abstract titles should be brief and reflect the content of the abstract.
[Background] Renal histology in IgA nephropathy (IgAN) and IgA vasculitis (IgAV) is often challenging to distinguish, because both are characterized by glomerulonephritis with IgA deposition. Macrophages contribute to the pathogenesis of vasculitis, and recent attention has been paid to the association between active renal vasculitis and M2 macrophages.
[Objective] To investigate renal pathological differences between IgAN and IgAV from the perspective of M2 macrophage infiltration.[Subjects and Methods] Renal biopsies were performed in 12 patients with IgAN (39±17 years old, 6 males) and 12 patients with IgAV (55±12 years old, 8 males). Proteinuria, degree of hematuria, eGFR, and histological findings (proportion of sclerotic glomeruli, crescents, and interstitial fibrosis) at the time of renal biopsy were compared between the two groups. Furthermore, CD163-positive cells stained by enzyme immunoassay were counted in all glomeruli and in the interstitium across over 30 consecutive high-power fields (400x). The mean number of positive cells in each compartment was calculated.
[Results] There were no significant differences between the IgAN and IgAV groups in proteinuria, degree of hematuria, eGFR, and histological findings (proportion of sclerotic glomeruli, crescents, and interstitial fibrosis) at the time of biopsy (p >0.05 for all). However, the numbers of CD163-positive cells in both glomeruli and interstitium were significantly higher in the IgAV group than in the IgAN group (4.2±2.8 vs. 0.7±0.7 cells/glomerulus, p<0.01; 8.2±4.6 vs. 2.7±1.8 cells/field, p<0.01).
[Conclusion] M2 macrophage infiltration into the glomeruli and interstitium was more pronounced in IgAV than in IgAN, suggesting its potential utility in the histopathological differentiation between the two conditions.