Prevalence, clinical significance, and persistence of autoantibodies in COVID-19

Virol J. 2023 Oct 16;20(1):236. doi: 10.1186/s12985-023-02191-z.

Abstract

Background: Interest in complications and sequelae following Coronavirus disease 2019 (COVID-19) is increasing. Several articles have reported COVID-19-associated autoimmune diseases and the association between autoantibodies and the severity of COVID-19. Thromboembolic complications are frequent in patients with COVID-19, and the anti-phospholipid antibodies (aPL) is frequently detected. We conducted this study to investigate the prevalence, clinical significance, and persistence of anti-nuclear antibodies (ANA) and aPLs in COVID-19.

Methods: We enrolled patients diagnosed with COVID-19 with oxygen demand and admitted to a tertiary hospital in South Korea between July 2020 and March 2022. ANA and aPLs levels were assessed using an immunoassay kit.

Results: A total of 248 patients were enrolled in the study. Among them, five patients were ANA-positive, and 41 were aPL-positive (IgM anti-cardiolipin (aCL) antibody in seven patients, IgG aCL in seven patients, IgM anti-β2Glycoprotein1 antibody (aβ2-GPI) in 32 patients, and IgG aβ2-GPI in one patient). Two of five ANA-positive patients, 13 of 32 IgM aβ2-GPI-positive patients, 5 of 7 IgM aCL-positive patients, and 2 of 7 IgG aCL-positive patients were eligible for follow-up analysis, and 100%, 69.2%, 40%, and 50% of the patients remained autoantibody-positive, respectively. There were no differences in clinical outcomes between the autoantibody-positive and autoantibody-negative groups, except for the IgG aCL group showing a tendency for worse outcomes.

Conclusion: A significant proportion of COVID-19 patients with oxygen demand were autoantibody-positive, and autoantibodies persisted for several months after symptom onset. Whether these autoantibodies are related to long-term sequelae in COVID-19 patients requires further investigation.

Keywords: Anti-nuclear antibody; Anti-phospholipid antibody; Autoantibody; COVID-19.

MeSH terms

  • Antibodies, Anticardiolipin
  • Autoantibodies*
  • COVID-19* / epidemiology
  • Clinical Relevance
  • Humans
  • Immunoglobulin G
  • Immunoglobulin M
  • Oxygen
  • Prevalence
  • beta 2-Glycoprotein I

Substances

  • Autoantibodies
  • beta 2-Glycoprotein I
  • Immunoglobulin G
  • Antibodies, Anticardiolipin
  • Immunoglobulin M
  • Oxygen