4.7 Article

Severe Coronavirus Disease 2019 (COVID-19) is Associated With Elevated Serum Immunoglobulin (Ig) A and Antiphospholipid IgA Antibodies

Journal

CLINICAL INFECTIOUS DISEASES
Volume 73, Issue 9, Pages E2869-E2874

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciaa1496

Keywords

COVID-19; immunoglobulin A; autoimmunity; antiphospholipid syndrome; thromboembolisms

Funding

  1. Swiss National Science Foundation [PP00P3_157448, P400PM_194473, PZ00P3_179919]
  2. Research Fund of the Kantonsspital St. Gallen [20/20]
  3. Promedica Foundation [1449/M]
  4. Swiss National Science Foundation (SNF) [PZ00P3_179919, P400PM_194473] Funding Source: Swiss National Science Foundation (SNF)

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This study found that severe COVID-19 patients have a vigorous total IgA response and higher levels of IgA antibodies, which may be associated with complications of severe illness. Additionally, severe illness in COVID-19 patients is significantly correlated with elevated levels of anticardiolipin antibodies, suggesting a potential link to systemic autoimmunity.
Background. Severe coronavirus disease 2019 (COVID-19) frequently entails complications that bear similarities to autoimmune diseases. To date, there are little data on possible immunoglobulin (Ig) A-mediated autoimmune responses. Here, we aim to determine whether COVID-19 is associated with a vigorous total IgA response and whether IgA antibodies are associated with complications of severe illness. Since thrombotic events are frequent in severe COVID-19 and resemble hypercoagulation of antiphospholipid syndrome, our approach focused on antiphospholipid antibodies (aPL). Methods. In this retrospective cohort study, clinical data and aPL from 64 patients with COVID-19 were compared from 3 independent tertiary hospitals (1 in Liechtenstein, 2 in Switzerland). Samples were collected from 9 April to 1 May 2020. Results. Clinical records of 64 patients with COVID-19 were reviewed and divided into a cohort with mild illness (mCOVID; 41%), a discovery cohort with severe illness (sdCOVID; 22%) and a confirmation cohort with severe illness (scCOVID; 38%). Total IgA, IgG, and aPL were measured with clinical diagnostic kits. Severe illness was significantly associated with increased total IgA (sdCOVID, P =.01; scCOVID, P <.001), but not total IgG. Among aPL, both cohorts with severe illness significantly correlated with elevated anticardiolipin IgA (sdCOVID and scCOVID, P <.001), anticardiolipin IgM (sdCOVID, P =.003; scCOVID, P <.001), and anti-beta 2 glycoprotein-1 IgA (sdCOVID and scCOVID, P <.001). Systemic lupus erythematosus was excluded from all patients as a potential confounder. Conclusions. Higher total IgA and IgA-aPL were consistently associated with severe illness. These novel data strongly suggest that a vigorous antiviral IgA response, possibly triggered in the bronchial mucosa, induces systemic autoimmunity.

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