Excessive neutrophil extracellular trap formation in ANCA-associated vasculitis is independent of ANCA

被引:79
作者
Kraaij, Tineke [1 ,2 ]
Kamerling, Sylvia W. A. [1 ]
van Dam, Laura S. [1 ,2 ]
Bakker, Jaap A. [3 ]
Bajema, Ingeborg M. [4 ]
Page, Theresa [5 ]
Brunini, Francesca [5 ]
Pusey, Charles D. [5 ]
Toes, Rene E. M. [6 ]
Scherer, Hans U. [2 ,6 ]
Rabelink, Ton J. [1 ,2 ]
van Kooten, Cees [1 ]
Teng, Y. K. Onno [1 ,2 ]
机构
[1] Leiden Univ, Dept Nephrol, Med Ctr, POB 9600, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Clin Lupus Vasculitis & Complementmediated Syst D, Leiden, Netherlands
[3] Leiden Univ, Med Ctr, Dept Clin Chem & Lab Med, Leiden, Netherlands
[4] Leiden Univ, Med Ctr, Dept Pathol, Leiden, Netherlands
[5] Imperial Coll London, Dept Renal Med, London, England
[6] Leiden Univ, Med Ctr, Dept Rheumatol, Leiden, Netherlands
关键词
ANCA-associated vasculitis; neutrophil extracellular traps; ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES; MEMBRANE PROTEINASE-3 EXPRESSION; LOW-DENSITY GRANULOCYTES; FC-GAMMA-RIIIB; NETTING NEUTROPHILS; DISEASE-ACTIVITY; MYELOPEROXIDASE; BIOMARKERS; MECHANISM; RITUXIMAB;
D O I
10.1016/j.kint.2018.01.013
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Neutrophil extracellular traps (NETs) are auto-antigenic strands of extracellular DNA covered with myeloperoxidase (MPO) and proteinase3 (PR3) that can be a source for the formation of anti-neutrophil cytoplasmic autoantibodies (ANCAs). The presence of NETs was recently demonstrated in renal tissue of patients with ANCA-associated vasculitis (AAV). NET formation was enhanced in AAV, suggesting that MPO-ANCA could trigger NET formation, supporting a vicious circle placing NETs in the center of AAV pathogenesis. Here we investigated NET formation in 99 patients with AAV by a novel highly sensitive and automated assay. There was a significant excess of ex vivo NET formation in both MPO-ANCA-and PR3-ANCApositive patients with AAV compared to healthy individuals. Excessive NET formation did not correlate with serum ANCA levels. Likewise, immunoglobulin G depletion had no effect on excessive NET formation in patients with AAV, indicating an ANCA-independent process. Next, we explored the relation of excessive NET formation to clinical disease in ten patients with AAV and showed that excessive NET formation was predominantly found during active disease, more so than during remission. Excessive NET formation was found in patients with AAV hospitalized for disease relapse but not during severe infection. Thus, excessive NET formation in AAV is independent of ANCA, and an excess of ex vivo NET formation was related to active clinical disease in patients with AAV and a marker of autoimmunity rather than infection.
引用
收藏
页码:139 / 149
页数:11
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