The development of anticyclic citrullinated peptide (anti‐CCP) antibody following severe COVID‐19

Author:

Roghani Seyed Askar123,Dastbaz Mohammad1,Lotfi Ramin45ORCID,Shamsi Afsaneh1,Abdan Zahra2,Rostampour Rezvan26,Soleymani Bijan3,Zamanian Mohammad Hossein2,Soufivand Parviz2,Pournazari Mehran2,Taghadosi Mahdi1ORCID

Affiliation:

1. Immunology Department, Faculty of Medicine Kermanshah University of Medical Sciences Kermanshah Iran

2. Clinical Research Development Center, Imam Reza Hospital Kermanshah University of Medical Sciences Kermanshah Iran

3. Medical Biology Research Center, Health Technology Institute Kermanshah University of Medical Sciences Kermanshah Iran

4. Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine Kurdistan Regional Blood Transfusion Center Sanandaj Iran

5. Clinical Research Development Center, Tohid Hospital Kurdistan University of Medical Sciences Sanandaj Iran

6. Department of Clinical Biochemistry, Medical School Kermanshah University of Medical Sciences Kermanshah Iran

Abstract

AbstractObjectivesThe dysregulated immune response is one of the cardinal features of severe coronavirus disease 2019 (COVID‐19). This study was conducted to clarify the occurrence of autoantibodies (AABs) associated with systemic autoimmune rheumatic diseases (SARDs) in hospitalized patients with a moderate, severe, and critical form of COVID‐19.MethodsThe serum samples obtained from 176 hospitalized COVID‐19 patients were investigated in this study, including patients with moderate (N = 90), severe (N = 50), and critical (N = 36) forms of COVID‐19. Also, the serum samples collected from healthy subjects before the COVID‐19 pandemic were used as controls (N = 176). The antinuclear antibodies (ANAs), antidouble‐stranded DNA (anti‐dsDNA), cytoplasmic‐anti neutrophil cytoplasmic antibody (c‐ANCA), perinuclear ANCA (p‐ANCA), antiphospholipid antibodies (aPLs), and anticyclic citrullinated peptide (anti‐CCP) occurrence was evaluated using a solid‐phase enzyme‐linked immunosorbent assay (ELISA).ResultsThe results showed that the occurrence of ANAs, anti‐dsDNA, anti‐CCP, c‐ANCA, and p‐ANCA was significantly higher in the COVID‐19 patients compared to serum obtained from healthy subjects (p < .0001, p < .0001, p < .0001, p < .05, and p < .001, respectively). The positive number of anti‐CCP tests increased significantly in severe COVID‐19 compared to the moderate group (p < .01).ConclusionOur study further supports the development of autoantibodies related to systemic autoimmune rheumatologic diseases. To the best of our knowledge, this is the first study with a large sample size that reported the occurrence of anti‐CCP in a severe form of COVID‐19.

Funder

Deputy for Research and Technology, Kermanshah University of Medical Sciences

Publisher

Wiley

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