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Intrinsically Distinct Role of Neutrophil Extracellular Trap Formation in Antineutrophil Cytoplasmic Antibody–Associated Vasculitis Compared to Systemic Lupus Erythematosus

OBJECTIVE: Different studies have demonstrated that neutrophil extracellular traps (NETs) may be involved in the pathophysiology of both antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis (AAV) and systemic lupus erythematosus (SLE). AAV and SLE are clinically and pathologically diverg...

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Autores principales: van Dam, Laura S., Kraaij, Tineke, Kamerling, Sylvia W. A., Bakker, Jaap A., Scherer, Uli H., Rabelink, Ton J., van Kooten, Cees, Teng, Y. K. Onno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7384043/
https://www.ncbi.nlm.nih.gov/pubmed/31313503
http://dx.doi.org/10.1002/art.41047
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author van Dam, Laura S.
Kraaij, Tineke
Kamerling, Sylvia W. A.
Bakker, Jaap A.
Scherer, Uli H.
Rabelink, Ton J.
van Kooten, Cees
Teng, Y. K. Onno
author_facet van Dam, Laura S.
Kraaij, Tineke
Kamerling, Sylvia W. A.
Bakker, Jaap A.
Scherer, Uli H.
Rabelink, Ton J.
van Kooten, Cees
Teng, Y. K. Onno
author_sort van Dam, Laura S.
collection PubMed
description OBJECTIVE: Different studies have demonstrated that neutrophil extracellular traps (NETs) may be involved in the pathophysiology of both antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis (AAV) and systemic lupus erythematosus (SLE). AAV and SLE are clinically and pathologically divergent autoimmune diseases with different autoantibodies. However, the respective autoantigens recognized in AAV and SLE have been shown to be an intricate part of NETs. This study aimed to examine whether the mechanisms of NET formation and the composition of NETs are distinct between AAV and SLE. METHODS: To investigate this hypothesis, healthy neutrophils were stimulated with serum from patients with AAV (n = 80) and patients with SLE (n = 59), and the mechanisms of NET formation and NET composition were compared. RESULTS: Both patients with AAV and patients with SLE had excessive NET formation, which correlated with the extent of disease activity (in AAV r = 0.5, P < 0.0001; in SLE r = 0.35, P < 0.01). Lytic NET formation over several hours was observed in patients with AAV, as compared to rapid (within minutes), non‐lytic NET formation coinciding with clustering of neutrophils in patients with SLE. AAV‐induced NET formation was triggered independent of IgG ANCAs, whereas SLE immune complexes (ICx) induced NET formation through Fcγ receptor signaling. AAV‐induced NET formation was dependent on reactive oxygen species and peptidyl arginine deaminases, and AAV‐induced NETs were enriched for citrullinated histones (mean ± SEM 23 ± 2%). In contrast, SLE‐induced NETs had immunogenic properties, including binding with high mobility group box chromosomal protein 1 (mean ± SEM 30 ± 3%) and enrichment for oxidized mitochondrial DNA, and were involved in ICx formation. CONCLUSION: The morphologic features, kinetics, induction pathways, and composition of excessive NET formation are all intrinsically distinct in AAV compared to SLE. Recognizing the diversity of NET formation between AAV and SLE provides a better understanding of the pathophysiologic role of NETs in these different autoimmune diseases.
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spelling pubmed-73840432020-07-28 Intrinsically Distinct Role of Neutrophil Extracellular Trap Formation in Antineutrophil Cytoplasmic Antibody–Associated Vasculitis Compared to Systemic Lupus Erythematosus van Dam, Laura S. Kraaij, Tineke Kamerling, Sylvia W. A. Bakker, Jaap A. Scherer, Uli H. Rabelink, Ton J. van Kooten, Cees Teng, Y. K. Onno Arthritis Rheumatol Systemic Lupus Erythematosus OBJECTIVE: Different studies have demonstrated that neutrophil extracellular traps (NETs) may be involved in the pathophysiology of both antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis (AAV) and systemic lupus erythematosus (SLE). AAV and SLE are clinically and pathologically divergent autoimmune diseases with different autoantibodies. However, the respective autoantigens recognized in AAV and SLE have been shown to be an intricate part of NETs. This study aimed to examine whether the mechanisms of NET formation and the composition of NETs are distinct between AAV and SLE. METHODS: To investigate this hypothesis, healthy neutrophils were stimulated with serum from patients with AAV (n = 80) and patients with SLE (n = 59), and the mechanisms of NET formation and NET composition were compared. RESULTS: Both patients with AAV and patients with SLE had excessive NET formation, which correlated with the extent of disease activity (in AAV r = 0.5, P < 0.0001; in SLE r = 0.35, P < 0.01). Lytic NET formation over several hours was observed in patients with AAV, as compared to rapid (within minutes), non‐lytic NET formation coinciding with clustering of neutrophils in patients with SLE. AAV‐induced NET formation was triggered independent of IgG ANCAs, whereas SLE immune complexes (ICx) induced NET formation through Fcγ receptor signaling. AAV‐induced NET formation was dependent on reactive oxygen species and peptidyl arginine deaminases, and AAV‐induced NETs were enriched for citrullinated histones (mean ± SEM 23 ± 2%). In contrast, SLE‐induced NETs had immunogenic properties, including binding with high mobility group box chromosomal protein 1 (mean ± SEM 30 ± 3%) and enrichment for oxidized mitochondrial DNA, and were involved in ICx formation. CONCLUSION: The morphologic features, kinetics, induction pathways, and composition of excessive NET formation are all intrinsically distinct in AAV compared to SLE. Recognizing the diversity of NET formation between AAV and SLE provides a better understanding of the pathophysiologic role of NETs in these different autoimmune diseases. John Wiley and Sons Inc. 2019-11-09 2019-12 /pmc/articles/PMC7384043/ /pubmed/31313503 http://dx.doi.org/10.1002/art.41047 Text en © 2019 The Authors. Arthritis & Rheumatology published by Wiley Periodicals, Inc. on behalf of American College of Rheumatology. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Systemic Lupus Erythematosus
van Dam, Laura S.
Kraaij, Tineke
Kamerling, Sylvia W. A.
Bakker, Jaap A.
Scherer, Uli H.
Rabelink, Ton J.
van Kooten, Cees
Teng, Y. K. Onno
Intrinsically Distinct Role of Neutrophil Extracellular Trap Formation in Antineutrophil Cytoplasmic Antibody–Associated Vasculitis Compared to Systemic Lupus Erythematosus
title Intrinsically Distinct Role of Neutrophil Extracellular Trap Formation in Antineutrophil Cytoplasmic Antibody–Associated Vasculitis Compared to Systemic Lupus Erythematosus
title_full Intrinsically Distinct Role of Neutrophil Extracellular Trap Formation in Antineutrophil Cytoplasmic Antibody–Associated Vasculitis Compared to Systemic Lupus Erythematosus
title_fullStr Intrinsically Distinct Role of Neutrophil Extracellular Trap Formation in Antineutrophil Cytoplasmic Antibody–Associated Vasculitis Compared to Systemic Lupus Erythematosus
title_full_unstemmed Intrinsically Distinct Role of Neutrophil Extracellular Trap Formation in Antineutrophil Cytoplasmic Antibody–Associated Vasculitis Compared to Systemic Lupus Erythematosus
title_short Intrinsically Distinct Role of Neutrophil Extracellular Trap Formation in Antineutrophil Cytoplasmic Antibody–Associated Vasculitis Compared to Systemic Lupus Erythematosus
title_sort intrinsically distinct role of neutrophil extracellular trap formation in antineutrophil cytoplasmic antibody–associated vasculitis compared to systemic lupus erythematosus
topic Systemic Lupus Erythematosus
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7384043/
https://www.ncbi.nlm.nih.gov/pubmed/31313503
http://dx.doi.org/10.1002/art.41047
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