Neutrophil extracellular traps drive peritoneal inflammation and tissue remodeling in pediatric peritoneal dialysis

Pediatr Nephrol. 2026 Mar;41(3):819-829. doi: 10.1007/s00467-025-07003-w. Epub 2025 Oct 18.

Abstract

Background: Peritoneal dialysis (PD) sustains children with chronic kidney disease stage 5 (CKD5) but promotes peritoneal membrane remodeling. Neutrophil extracellular traps (NETs) orchestrate antimicrobial defense and sterile inflammation; their involvement in PD-induced transformation is unknown.

Methods: Forty-five children were enrolled in the International Pediatric Peritoneal Biobank. Peritoneal biopsies taken at PD initiation and after ≥ 12 months of low-glucose-degradation-product PD were compared with surgical biopsies from non-uremic peers. Histomorphometry quantified microvessel density, submesothelial thickness, leukocyte infiltration, collagen I/III, and NET markers (citrullinated histone H3, neutrophil elastase, myeloperoxidase). Dialysate and plasma collected every 2 months for 18 months were assayed for cell-free DNA, NET proteins, DNase1, and DNase1L3.

Results: After chronic PD, the peritoneum displayed doubled microvessel density, tripled submesothelial thickness, and marked immune-cell infiltration (all p < 0.01). NET structures were prominent in tissue, while dialysate and plasma concentrations of cell-free DNA, citrullinated histone H3, neutrophil elastase, and myeloperoxidase increased two- to fourfold versus baseline (p < 0.05). DNase1 levels correlated with membrane thickness (r = 0.46, p = 0.003) and DNase1L3 with vascular density (r = 0.51, p = 0.001), suggesting limited compensatory NET clearance.

Conclusions: Chronic PD elicits NET-driven sterile inflammation that parallels structural remodeling of the pediatric peritoneum. Supplementing PD fluids with exogenous NET-degrading enzymes may preserve membrane integrity and prolong PD suitability in children.

Keywords: Children; DNase1 and DNase1L3; Neutrophil extracellular traps; Peritoneal dialysis.

MeSH terms

  • Adolescent
  • Biopsy
  • Child
  • Child, Preschool
  • Deoxyribonuclease I / metabolism
  • Dialysis Solutions
  • Extracellular Traps* / immunology
  • Extracellular Traps* / metabolism
  • Female
  • Histones / metabolism
  • Humans
  • Infant
  • Kidney Failure, Chronic / therapy
  • Male
  • Neutrophils / immunology
  • Peritoneal Dialysis* / adverse effects
  • Peritoneum* / blood supply
  • Peritoneum* / immunology
  • Peritoneum* / metabolism
  • Peritoneum* / pathology
  • Peritonitis* / etiology
  • Peritonitis* / immunology
  • Peritonitis* / pathology

Substances

  • Dialysis Solutions
  • Deoxyribonuclease I
  • Histones

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