Distinct subsets of anti-pulmonary autoantibodies correlate with disease severity and survival in severe COVID-19 patients

Author:

Tóth Emese,Fagyas Miklós,Nagy Béla,Siket Ivetta Mányiné,Szőke Blanka,Mártha Lilla,Mahdi Mohamed,Erdősi Gábor,Pólik Zsófia,Kappelmayer János,Papp Zoltán,Borbély Attila,Szabó Tamás,Balla József,Balla György,Bácsi Attila,Szekanecz Zoltán,Bai Péter,Tóth AttilaORCID

Abstract

AbstractAutoantibodies targeting the lung tissue were identified in severe COVID-19 patients in this retrospective study. Fifty-three percent of 104 patients developed anti-pulmonary antibodies, the majority of which were IgM class, suggesting that they developed upon infection with SARS-CoV-2. Anti-pulmonary antibodies correlated with worse pulmonary function and a higher risk of multiorgan failure that was further aggravated if 3 or more autoantibody clones were simultaneously present (multi-producers). Multi-producer patients were older than the patients with less or no autoantibodies. One of the identified autoantibodies (targeting a pulmonary protein of ~ 50 kDa) associated with worse clinical outcomes, including mortality. In summary, severe COVID-19 is associated with the development of lung-specific autoantibodies, which may worsen the clinical outcome. Tissue proteome-wide tests, such as the ones applied here, can be used to detect autoimmunity in the post-COVID state to identify the cause of symptoms and to reveal a new target for treatment.

Funder

Hungarian Academy of Sciences

Magyar Tudományos Akadémia

Hungarian Scientific Research Fund

National Research, Development and Innovation Office

NKFIH

University of Debrecen

Publisher

Springer Science and Business Media LLC

Subject

Geriatrics and Gerontology,Aging

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