Neutrophil extracellular trap formation in anti-neutrophil cytoplasmic antibody-associated and large-vessel vasculitis

Clin Immunol. 2023 Apr:249:109274. doi: 10.1016/j.clim.2023.109274. Epub 2023 Mar 4.

Abstract

Levels of neutrophil extracellular traps (NETs) were measured in plasma of healthy controls (HC, n = 30) and patients with granulomatosis with polyangiitis (GPA, n = 123), microscopic polyangiitis (MPA, n = 61), Takayasu's arteritis (TAK, n = 58), and giant cell arteritis (GCA, n = 68), at times of remission or activity and correlated with levels of the platelet-derived thrombospondin-1 (TSP-1). Levels of NETs were elevated during active disease in patients with GPA (p < 0.0001), MPA (p = 0.0038), TAK (p < 0.0001), and GCA (p < 0.0001), and in remission for GPA, p < 0.0001, MPA, p = 0.005, TAK, p = 0.03, and GCA, p = 0.0009. All cohorts demonstrated impaired NET degradation. Patients with GPA (p = 0.0045) and MPA (p = 0.005) had anti-NET IgG antibodies. Patients with TAK had anti-histone antibodies (p < 0.01), correlating with presence of NETs. Levels of TSP-1 were increased in all patients with vasculitis, and associated with NET formation. NET formation is a common process in vasculitides. Targeting NET formation or degradation could be potential therapeutic approaches for vasculitides.

Keywords: Anti-neutrophil cytoplasmic antibody associated vasculitis; Histone; Large vessel vasculitis; Neutrophil extracellular traps; Neutrophils; Platelet activation; Thrombospondin-1.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis* / drug therapy
  • Case-Control Studies
  • Child
  • Extracellular Traps* / metabolism
  • Female
  • Giant Cell Arteritis* / metabolism
  • Granulomatosis with Polyangiitis* / metabolism
  • Humans
  • Male
  • Microscopic Polyangiitis* / metabolism
  • Middle Aged
  • Neutrophils
  • Takayasu Arteritis* / metabolism
  • Thrombospondin 1* / metabolism

Substances

  • Thrombospondin 1