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254. Clinical significance of antineutrophil cytoplasmic antibody positivity in patients infected with SARS-CoV-2

BACKGROUND: The Coronavirus Disease 2019 (COVID-19) is well-known for its broad spectrum of immune-related phenotypes similar to those seen in autoimmune or inflammatory diseases. Furthermore, evidence has gradually accumulated that COVID-19 may induce systemic inflammatory manifestations such as mu...

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Autores principales: Lee, Lucy Eunju, Jeong, Wooyong, Park, Yong-Beom, Jeong, Su Jin, Lee, Sang-Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9752857/
http://dx.doi.org/10.1093/ofid/ofac492.332
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author Lee, Lucy Eunju
Jeong, Wooyong
Park, Yong-Beom
Jeong, Su Jin
Lee, Sang-Won
author_facet Lee, Lucy Eunju
Jeong, Wooyong
Park, Yong-Beom
Jeong, Su Jin
Lee, Sang-Won
author_sort Lee, Lucy Eunju
collection PubMed
description BACKGROUND: The Coronavirus Disease 2019 (COVID-19) is well-known for its broad spectrum of immune-related phenotypes similar to those seen in autoimmune or inflammatory diseases. Furthermore, evidence has gradually accumulated that COVID-19 may induce systemic inflammatory manifestations such as multisystem inflammatory syndrome, haemophagocytic syndromes, and systemic vasculitis. Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a small vessel vasculitis characterised by necrotising vasculitis. So far, there have been several case reports regarding AAV occurrence after severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, which have indicated a triggering potential of SARS-CoV-2 infection for AAV occurrence. This study investigated the rate of ANCA positivity and its clinical significance in COVID-19 patients. METHODS: This study included 178 patients infected with SARS-CoV-2 who were enrolled in a cohort of a single center. Myeloperoxidase (MPO)-ANCA and proteinase 3 (PR3)-ANCA from the stored blood sera were measured using the immunoassay kits. Mortality, mechanical ventilator care, and severe infection were assessed as poor outcomes. Severe infection was defined as a medical condition that required a high-flow nasal cannula and/or mechanical ventilator care. The 2022 American College of Rheumatology and the European Alliance of Associations for Rheumatology classification criteria for the three subtypes of AAV were applied only to patients who had MPO-ANCA or PR3-ANCA among the study subjects RESULTS: The detection rate of ANCA positivity was 18.5%: MPO-ANCA and PR3-ANCA were found in 22 (12.4%) and 14 (7.9%) patients. Patients with ANCA positivity exhibited a lower cumulative survival rate than those without, but the difference was not statistically significant (P = 0.057). However, neither MPO-ANCA nor PR3-ANCA affected the three poor outcomes. According to the new criteria, 12 (6.7%) and 21 (11.8%) patients were classified as having granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA) [Figure: see text] [Figure: see text] [Figure: see text] Neither ANCA positivity nor ANCA subtype (MPO-ANCA and PR3-ANCA) positivity had a significant influence on poor outcomes of SARS-CoV-2. ANCA: antineutrophil cytoplasmic antibody; MPO: myeloperoxidase; PR3: proteinase 3; SARS-CoV-2: severe acute respiratory syndrome coronavirus 2. CONCLUSION: SARS-CoV-2 infection may increase the rate of ANCA positivity, which may not affect poor outcomes but contribute to the classification of GPA and MPA despite uncertain clinical significance DISCLOSURES: All Authors: No reported disclosures.
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spelling pubmed-97528572022-12-16 254. Clinical significance of antineutrophil cytoplasmic antibody positivity in patients infected with SARS-CoV-2 Lee, Lucy Eunju Jeong, Wooyong Park, Yong-Beom Jeong, Su Jin Lee, Sang-Won Open Forum Infect Dis Abstracts BACKGROUND: The Coronavirus Disease 2019 (COVID-19) is well-known for its broad spectrum of immune-related phenotypes similar to those seen in autoimmune or inflammatory diseases. Furthermore, evidence has gradually accumulated that COVID-19 may induce systemic inflammatory manifestations such as multisystem inflammatory syndrome, haemophagocytic syndromes, and systemic vasculitis. Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a small vessel vasculitis characterised by necrotising vasculitis. So far, there have been several case reports regarding AAV occurrence after severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, which have indicated a triggering potential of SARS-CoV-2 infection for AAV occurrence. This study investigated the rate of ANCA positivity and its clinical significance in COVID-19 patients. METHODS: This study included 178 patients infected with SARS-CoV-2 who were enrolled in a cohort of a single center. Myeloperoxidase (MPO)-ANCA and proteinase 3 (PR3)-ANCA from the stored blood sera were measured using the immunoassay kits. Mortality, mechanical ventilator care, and severe infection were assessed as poor outcomes. Severe infection was defined as a medical condition that required a high-flow nasal cannula and/or mechanical ventilator care. The 2022 American College of Rheumatology and the European Alliance of Associations for Rheumatology classification criteria for the three subtypes of AAV were applied only to patients who had MPO-ANCA or PR3-ANCA among the study subjects RESULTS: The detection rate of ANCA positivity was 18.5%: MPO-ANCA and PR3-ANCA were found in 22 (12.4%) and 14 (7.9%) patients. Patients with ANCA positivity exhibited a lower cumulative survival rate than those without, but the difference was not statistically significant (P = 0.057). However, neither MPO-ANCA nor PR3-ANCA affected the three poor outcomes. According to the new criteria, 12 (6.7%) and 21 (11.8%) patients were classified as having granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA) [Figure: see text] [Figure: see text] [Figure: see text] Neither ANCA positivity nor ANCA subtype (MPO-ANCA and PR3-ANCA) positivity had a significant influence on poor outcomes of SARS-CoV-2. ANCA: antineutrophil cytoplasmic antibody; MPO: myeloperoxidase; PR3: proteinase 3; SARS-CoV-2: severe acute respiratory syndrome coronavirus 2. CONCLUSION: SARS-CoV-2 infection may increase the rate of ANCA positivity, which may not affect poor outcomes but contribute to the classification of GPA and MPA despite uncertain clinical significance DISCLOSURES: All Authors: No reported disclosures. Oxford University Press 2022-12-15 /pmc/articles/PMC9752857/ http://dx.doi.org/10.1093/ofid/ofac492.332 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstracts
Lee, Lucy Eunju
Jeong, Wooyong
Park, Yong-Beom
Jeong, Su Jin
Lee, Sang-Won
254. Clinical significance of antineutrophil cytoplasmic antibody positivity in patients infected with SARS-CoV-2
title 254. Clinical significance of antineutrophil cytoplasmic antibody positivity in patients infected with SARS-CoV-2
title_full 254. Clinical significance of antineutrophil cytoplasmic antibody positivity in patients infected with SARS-CoV-2
title_fullStr 254. Clinical significance of antineutrophil cytoplasmic antibody positivity in patients infected with SARS-CoV-2
title_full_unstemmed 254. Clinical significance of antineutrophil cytoplasmic antibody positivity in patients infected with SARS-CoV-2
title_short 254. Clinical significance of antineutrophil cytoplasmic antibody positivity in patients infected with SARS-CoV-2
title_sort 254. clinical significance of antineutrophil cytoplasmic antibody positivity in patients infected with sars-cov-2
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9752857/
http://dx.doi.org/10.1093/ofid/ofac492.332
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