Abundant Glomerular Neutrophil Extracellular Traps in C3 Glomerulopathy

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Abstract

Introduction

C3 glomerulopathy (C3G) is driven by fluid-phase alternative complement pathway dysregulation, with emerging evidence linking glomerular neutrophil infiltration to disease severity. Neutrophil extracellular traps (NETs) are implicated in other forms of glomerulonephritis. However, their participation in the pathogenesis of C3G remains undefined.

Methods

Kidney biopsies from 33 patients with C3G (15 with dense deposit disease [DDD] and 18 with C3 glomerulonephritis [C3GN]) were compared with 15 anti-neutrophil cytoplasmic antibody associated vasculitis (AAV) biopsies as a neutrophil-rich disease control in this retrospective cross-sectional study. Glomerular neutrophils and NETs were identified using immunofluorescence, staining for myeloperoxidase, citrullinated histone H3, peptidyl arginine deiminase-4, and DNA. Supervised machine learning was used to quantify glomerular NET formation, and the data were correlated with kidney function at time of biopsy using linear regression.

Results

Intraglomerular NETs were abundant and detected in the majority of glomeruli in C3G biopsies. Compared with AAV, C3G showed a significantly higher fraction of neutrophils forming NETs, despite similar neutrophil counts per glomerulus. NET abundance was similar in DDD and C3GN. In exploratory analyses, a greater proportion of glomeruli containing NETs was associated with lower kidney function (estimated glomerular filtration rate) at biopsy, and this association remained significant after adjustment for age, C3G subtype, and interstitial fibrosis.

Conclusions

These observations demonstrate that intraglomerular NETs are a common and prominent observation in C3G and are associated with reduced kidney function at biopsy. These findings raise the possibility that NET deposition in glomeruli is a previously unrecognized driver of glomerular injury in C3G.

TRANSLATIONAL STATEMENT

Targeted complement inhibitors have expanded treatment options for C3 glomerulopathy, but treatment responses remain incomplete and the cellular processes accompanying active intrarenal injury remain incompletely defined. We examined renal biopsies of C3G patients for neutrophil infiltration / recruitment and release of neutrophil extracellular traps (NETs) and found that these structures were highly abundant in glomeruli. Greater glomerular NET burden was associated with lower estimated glomerular filtration rate at biopsy. Our observations identify NETs as a candidate component of the pathogenesis of glomerular pathology in C3G and support the investigation of NET-targeting interventions in addition to complement inhibition in C3G patients.

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