Assessment of longitudinal serum neutrophil extracellular trap–inducing activity in anti-neutrophil cytoplasmic antibody–associated vasculitis and glomerulonephritis in a prospective cohort using a novel bio-impedance technique

医学 中性粒细胞胞外陷阱 前瞻性队列研究 抗体 免疫学 抗中性粒细胞胞浆抗体 血管炎 内科学 中性粒细胞 肾小球肾炎 队列 系统性血管炎 细胞外 细胞质 病理 炎症 疾病 化学 生物化学
作者
Joop P. Aendekerk,Renée Ysermans,Matthias H. Busch,Ruud Theunissen,Nele Bijnens,Judith Potjewijd,Jan Damoiseaux,Chris Reutelingsperger,Pieter van Paassen
出处
期刊:Kidney International [Elsevier BV]
卷期号:104 (1): 151-162 被引量:8
标识
DOI:10.1016/j.kint.2023.03.029
摘要

Neutrophil extracellular traps (NET) have been implicated in the pathogenesis of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV). Here, we developed a novel, label-free, high-throughput bio-impedance technique to effectively measure serum NET-inducing activity. Using this technique, NET-inducing activity of serum derived from patients with AAV was assessed in a prospective cohort of 62 patients presenting with active AAV with major organ involvement. Thirty-five patients presented with new and 27 patients presented with relapsing AAV, of whom 38 had kidney and/or 31 had lung involvement. NET-inducing activity was assessed at diagnosis of active AAV (time zero), during the first 6 weeks of treatment, and after 6 months of treatment. Forty-seven patients revealed elevated NET-inducing activity at time zero. After initiation of immunosuppressive treatment, NET-inducing activity was reduced at six weeks. A subsequent increase at six months could potentially identify patients with relapsing disease (hazard ratio, 11.45 [interquartile range 1.36-96.74]). NET-inducing activity at time zero correlated with kidney function and proteinuria. Importantly, in kidney tissue, NETs co-localized with lesions typical of ANCA-associated glomerulonephritis and even correlated with systemic serum NET-inducing activity. Thus, our prospective data corroborate the importance of NET formation in AAV and ANCA-associated glomerulonephritis and the potential of longitudinal evaluation, as monitored by our novel bio-impedance assay and detailed histological evaluation.
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