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Association of Sputum Neutrophil Extracellular Trap Subsets With IgA Anti–Citrullinated Protein Antibodies in Subjects at Risk for Rheumatoid Arthritis

OBJECTIVE: Mechanisms leading to anti–citrullinated protein antibody (ACPA) generation in rheumatoid arthritis (RA) are hypothesized to originate in the lung. We undertook this study to understand associations between neutrophil extracellular trap (NET) formation in the lung and local ACPA generatio...

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Autores principales: Okamoto, Yuko, Devoe, Stephanie, Seto, Nickie, Minarchick, Valerie, Wilson, Timothy, Rothfuss, Heather M., Mohning, Michael P., Arbet, Jaron, Kroehl, Miranda, Visser, Ashley, August, Justin, Thomas, Stacey M., Charry, Laura Lenis, Fleischer, Chelsie, Feser, Marie L., Frazer‐Abel, Ashley A., Norris, Jill M., Cherrington, Brian D., Janssen, William J., Kaplan, Mariana J., Deane, Kevin D., Holers, V. Michael, Demoruelle, M. Kristen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8712364/
https://www.ncbi.nlm.nih.gov/pubmed/34369110
http://dx.doi.org/10.1002/art.41948
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author Okamoto, Yuko
Devoe, Stephanie
Seto, Nickie
Minarchick, Valerie
Wilson, Timothy
Rothfuss, Heather M.
Mohning, Michael P.
Arbet, Jaron
Kroehl, Miranda
Visser, Ashley
August, Justin
Thomas, Stacey M.
Charry, Laura Lenis
Fleischer, Chelsie
Feser, Marie L.
Frazer‐Abel, Ashley A.
Norris, Jill M.
Cherrington, Brian D.
Janssen, William J.
Kaplan, Mariana J.
Deane, Kevin D.
Holers, V. Michael
Demoruelle, M. Kristen
author_facet Okamoto, Yuko
Devoe, Stephanie
Seto, Nickie
Minarchick, Valerie
Wilson, Timothy
Rothfuss, Heather M.
Mohning, Michael P.
Arbet, Jaron
Kroehl, Miranda
Visser, Ashley
August, Justin
Thomas, Stacey M.
Charry, Laura Lenis
Fleischer, Chelsie
Feser, Marie L.
Frazer‐Abel, Ashley A.
Norris, Jill M.
Cherrington, Brian D.
Janssen, William J.
Kaplan, Mariana J.
Deane, Kevin D.
Holers, V. Michael
Demoruelle, M. Kristen
author_sort Okamoto, Yuko
collection PubMed
description OBJECTIVE: Mechanisms leading to anti–citrullinated protein antibody (ACPA) generation in rheumatoid arthritis (RA) are hypothesized to originate in the lung. We undertook this study to understand associations between neutrophil extracellular trap (NET) formation in the lung and local ACPA generation in subjects at risk of developing RA. METHODS: Induced sputum was collected from 49 subjects at risk of developing RA, 12 patients with RA, and 18 controls. Sputum neutrophils were tested for ex vivo NET formation, and sputum‐induced NET formation of control neutrophils was measured using immunofluorescence imaging. Sputum macrophages were tested for ex vivo endocytosis of apoptotic and opsonized cells. Levels of ACPA, NET remnants, and inflammatory proteins were quantified in sputum supernatant. RESULTS: Spontaneous citrullinated histone H3 (Cit‐H3)–expressing NET formation was higher in sputum neutrophils from at‐risk subjects and RA patients compared to controls (median 12%, 22%, and 0%, respectively; P < 0.01). In at‐risk subjects, sputum IgA ACPA correlated with the percentage of neutrophils that underwent Cit‐H3+ NET formation (r = 0.49, P = 0.002) and levels of Cit‐H3+ NET remnants (r = 0.70, P < 0.001). Reduced endocytic capacity of sputum macrophages was found in at‐risk subjects and RA patients compared to controls. Using a mediation model, we found that sputum inflammatory proteins were associated with sputum IgA ACPA through a pathway mediated by Cit‐H3+ NET remnants. Sputum‐induced Cit‐H3+ NET formation also correlated with sputum levels of interleukin‐1β (IL‐1β), IL‐6, and tumor necrosis factor in at‐risk subjects, suggesting a causal relationship. CONCLUSION: These data support a potential mechanism for mucosal ACPA generation in subjects at risk of developing RA, whereby inflammation leads to increased citrullinated protein–expressing NETs that promote local ACPA generation.
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spelling pubmed-87123642022-10-14 Association of Sputum Neutrophil Extracellular Trap Subsets With IgA Anti–Citrullinated Protein Antibodies in Subjects at Risk for Rheumatoid Arthritis Okamoto, Yuko Devoe, Stephanie Seto, Nickie Minarchick, Valerie Wilson, Timothy Rothfuss, Heather M. Mohning, Michael P. Arbet, Jaron Kroehl, Miranda Visser, Ashley August, Justin Thomas, Stacey M. Charry, Laura Lenis Fleischer, Chelsie Feser, Marie L. Frazer‐Abel, Ashley A. Norris, Jill M. Cherrington, Brian D. Janssen, William J. Kaplan, Mariana J. Deane, Kevin D. Holers, V. Michael Demoruelle, M. Kristen Arthritis Rheumatol Rheumatoid Arthritis OBJECTIVE: Mechanisms leading to anti–citrullinated protein antibody (ACPA) generation in rheumatoid arthritis (RA) are hypothesized to originate in the lung. We undertook this study to understand associations between neutrophil extracellular trap (NET) formation in the lung and local ACPA generation in subjects at risk of developing RA. METHODS: Induced sputum was collected from 49 subjects at risk of developing RA, 12 patients with RA, and 18 controls. Sputum neutrophils were tested for ex vivo NET formation, and sputum‐induced NET formation of control neutrophils was measured using immunofluorescence imaging. Sputum macrophages were tested for ex vivo endocytosis of apoptotic and opsonized cells. Levels of ACPA, NET remnants, and inflammatory proteins were quantified in sputum supernatant. RESULTS: Spontaneous citrullinated histone H3 (Cit‐H3)–expressing NET formation was higher in sputum neutrophils from at‐risk subjects and RA patients compared to controls (median 12%, 22%, and 0%, respectively; P < 0.01). In at‐risk subjects, sputum IgA ACPA correlated with the percentage of neutrophils that underwent Cit‐H3+ NET formation (r = 0.49, P = 0.002) and levels of Cit‐H3+ NET remnants (r = 0.70, P < 0.001). Reduced endocytic capacity of sputum macrophages was found in at‐risk subjects and RA patients compared to controls. Using a mediation model, we found that sputum inflammatory proteins were associated with sputum IgA ACPA through a pathway mediated by Cit‐H3+ NET remnants. Sputum‐induced Cit‐H3+ NET formation also correlated with sputum levels of interleukin‐1β (IL‐1β), IL‐6, and tumor necrosis factor in at‐risk subjects, suggesting a causal relationship. CONCLUSION: These data support a potential mechanism for mucosal ACPA generation in subjects at risk of developing RA, whereby inflammation leads to increased citrullinated protein–expressing NETs that promote local ACPA generation. John Wiley and Sons Inc. 2021-11-25 2022-01 /pmc/articles/PMC8712364/ /pubmed/34369110 http://dx.doi.org/10.1002/art.41948 Text en © 2021 The Authors. Arthritis & Rheumatology published by Wiley Periodicals LLC on behalf of American College of Rheumatology. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://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 Rheumatoid Arthritis
Okamoto, Yuko
Devoe, Stephanie
Seto, Nickie
Minarchick, Valerie
Wilson, Timothy
Rothfuss, Heather M.
Mohning, Michael P.
Arbet, Jaron
Kroehl, Miranda
Visser, Ashley
August, Justin
Thomas, Stacey M.
Charry, Laura Lenis
Fleischer, Chelsie
Feser, Marie L.
Frazer‐Abel, Ashley A.
Norris, Jill M.
Cherrington, Brian D.
Janssen, William J.
Kaplan, Mariana J.
Deane, Kevin D.
Holers, V. Michael
Demoruelle, M. Kristen
Association of Sputum Neutrophil Extracellular Trap Subsets With IgA Anti–Citrullinated Protein Antibodies in Subjects at Risk for Rheumatoid Arthritis
title Association of Sputum Neutrophil Extracellular Trap Subsets With IgA Anti–Citrullinated Protein Antibodies in Subjects at Risk for Rheumatoid Arthritis
title_full Association of Sputum Neutrophil Extracellular Trap Subsets With IgA Anti–Citrullinated Protein Antibodies in Subjects at Risk for Rheumatoid Arthritis
title_fullStr Association of Sputum Neutrophil Extracellular Trap Subsets With IgA Anti–Citrullinated Protein Antibodies in Subjects at Risk for Rheumatoid Arthritis
title_full_unstemmed Association of Sputum Neutrophil Extracellular Trap Subsets With IgA Anti–Citrullinated Protein Antibodies in Subjects at Risk for Rheumatoid Arthritis
title_short Association of Sputum Neutrophil Extracellular Trap Subsets With IgA Anti–Citrullinated Protein Antibodies in Subjects at Risk for Rheumatoid Arthritis
title_sort association of sputum neutrophil extracellular trap subsets with iga anti–citrullinated protein antibodies in subjects at risk for rheumatoid arthritis
topic Rheumatoid Arthritis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8712364/
https://www.ncbi.nlm.nih.gov/pubmed/34369110
http://dx.doi.org/10.1002/art.41948
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