Investigation of Anti-Neutrophil Cytoplasmic Antibody by Indirect Immunofluorescence Assay in Covid-19 Patients

dc.contributor.author Ayaydın, Zeynep
dc.contributor.author Ozcan, Nida
dc.contributor.author Mermutluoglu, Cigdem
dc.contributor.author Atmaca, Selahattin
dc.contributor.author Tekin, Ali Cem
dc.contributor.other Department of Basic Medical Sciences / Temel Tıp Bilimleri Bölümü
dc.contributor.other 10. Faculty of Medicine / Tıp Fakültesi
dc.contributor.other 01. Mardin Artuklu University / Mardin Artuklu Üniversitesi
dc.date.accessioned 2025-07-02T11:46:38Z
dc.date.available 2025-07-02T11:46:38Z
dc.date.issued 2025
dc.description.abstract Aim: Coronavirus disease-2019 (COVID-19) has been suggested to trigger the production of autoimmune antibodies and contribute to the development of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis. This study aims to investigate the presence of ANCA among COVID-19 patients. Methods: This cross-sectional, prospective analysis included 200 COVID-19 patients with positive polymerase chain reaction test results for severe acute respiratory syndrome-coronavirus-2 and no history of autoimmune disease, recruited between June 2021 and November 2022. The control group included 50 age-matched healthy blood donors. The ANCA profile was assessed using the indirect immunofluorescence assay method with the EUROPLUS Granulocyte Mosaic EUROPattern test kit (EUROIMMUN, Germany) on sera samples of the patient and control groups. Results: Perinuclear ANCA (p-ANCA) was detected in 12 of 200 COVID-19 patients (6.0%) and cytoplasmic ANCA (c-ANCA) was detected in 15 of 200 patients (7.5%). No ANCA positivity was observed in the control group (0/50). ANCA positivity among COVID-19 patients (27 of 200, 13.5%) was statistically significantly higher than in the control group (p<0.05). ANCA positivity was significantly higher in intensive care unit (ICU) patients (21 of 77, 27.3%) compared to non-ICU patients (6 of 123, 4.9%) (p<0.05). Conclusion: ANCA presence in ICU patients supports the hypothesis that COVID-19 triggers ANCA synthesis and contributes to disease severity. en_US
dc.description.sponsorship Dicle University Scientific Research Projects Commission (DUBAP) [SBE.21.005] en_US
dc.description.sponsorship Financial Disclosure: This study was supported by the Dicle University Scientific Research Projects Commission (DUBAP) under project number SBE.21.005. en_US
dc.identifier.doi 10.4274/haseki.galenos.2025.9879
dc.identifier.issn 1302-0072
dc.identifier.issn 2147-2688
dc.identifier.scopus 2-s2.0-105005103536
dc.identifier.uri https://doi.org/10.4274/haseki.galenos.2025.9879
dc.identifier.uri https://hdl.handle.net/20.500.12514/8930
dc.language.iso en en_US
dc.publisher Galenos Publ House en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Covid-19 en_US
dc.subject Anti-Neutrophil Cytoplasmic Antibodies en_US
dc.subject Vasculitis en_US
dc.subject Indirect Immunofluorescence Assay en_US
dc.title Investigation of Anti-Neutrophil Cytoplasmic Antibody by Indirect Immunofluorescence Assay in Covid-19 Patients en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.scopusid 56109034100
gdc.author.scopusid 55735770700
gdc.author.scopusid 57193026231
gdc.author.scopusid 7003992084
gdc.author.scopusid 59252654800
gdc.author.wosid Ayaydin, Zeynep/Lxb-1183-2024
gdc.author.wosid Mermutluoglu, Cigdem/Hiz-7042-2022
gdc.description.department Artuklu University en_US
gdc.description.departmenttemp [Ayaydin, Zeynep] Mardin Artuklu Univ, Fac Med, Dept Med Microbiol, Mardin, Turkiye; [Ozcan, Nida; Atmaca, Selahattin] Dicle Univ, Fac Med, Dept Med Microbiol, Diyarbakir, Turkiye; [Mermutluoglu, Cigdem] Dicle Univ, Fac Med, Dept Infect Dis & Clin Microbiol, Diyarbakir, Turkiye; [Tekin, Ali Cem] Univ Hlth Sci Turkey, Gazi Yasargil Training & Res Hosp, Dept Med Microbiol, Diyarbakir, Turkiye en_US
gdc.description.endpage 23 en_US
gdc.description.issue 1 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q3
gdc.description.startpage 19 en_US
gdc.description.volume 63 en_US
gdc.description.woscitationindex Emerging Sources Citation Index
gdc.description.wosquality N/A
gdc.identifier.wos WOS:001484059000001
gdc.scopus.citedcount 0
gdc.wos.citedcount 0
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