Neutrophil single-cell analysis identifies a type II interferon-related subset for predicting relapse of autoimmune small vessel vasculitis

Nat Commun. 2025 Apr 24;16(1):3581. doi: 10.1038/s41467-025-58550-7.

Abstract

To identify the dynamics of neutrophil autoimmunity, here we focus on anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis and perform single-cell transcriptome and surface proteome analyses on peripheral white blood cells from patients with new-onset microscopic polyangiitis (MPA). Compared with controls, two neutrophil populations, immature neutrophils and neutrophils with type II interferon signature genes (Neu_T2ISG), are increased in patients with MPA. Trajectory and cell-cell interaction analyses identify Neu_T2ISG as a subset that differentiates from mature neutrophils upon stimulation with IFN-γ and TNF, which synergize to induce myeloperoxidase and Fcγ receptors expression on the neutrophil cell surface and promote ANCA-induced neutrophil extracellular trap formation. Case-by-case analysis indicates that patients with a high proportion of the Neu_T2ISG subset are associated with persistent vasculitis symptoms. A larger cohort analysis shows that serum IFN-γ levels at disease onset correlate with susceptibility to disease relapse. Our findings thus identify neutrophil diversity at the single cell level and implicate a biomarker for predicting relapse in small vessel vasculitis.

MeSH terms

  • Adult
  • Aged
  • Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis* / blood
  • Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis* / immunology
  • Antibodies, Antineutrophil Cytoplasmic / immunology
  • Biomarkers / blood
  • Case-Control Studies
  • Extracellular Traps / immunology
  • Extracellular Traps / metabolism
  • Female
  • Humans
  • Interferon-gamma* / blood
  • Interferon-gamma* / immunology
  • Interferon-gamma* / metabolism
  • Male
  • Microscopic Polyangiitis* / blood
  • Microscopic Polyangiitis* / genetics
  • Microscopic Polyangiitis* / immunology
  • Middle Aged
  • Neutrophils* / immunology
  • Neutrophils* / metabolism
  • Peroxidase / metabolism
  • Receptors, IgG / metabolism
  • Recurrence
  • Single-Cell Analysis / methods
  • Transcriptome
  • Tumor Necrosis Factor-alpha

Substances

  • Interferon-gamma
  • Antibodies, Antineutrophil Cytoplasmic
  • Peroxidase
  • Biomarkers
  • Receptors, IgG
  • Tumor Necrosis Factor-alpha