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SARS-CoV-2 infection induces the production of autoantibodies in severe COVID-19 patients in an age-dependent manner

Fonseca, D. L. M.; Filgueiras, I. S.; Marques, A. H.; Vojdani, E.; Halpert, G.; Ostrinski, Y.; Baiocchi, G. C.; Placa, D. R.; Freire, P. P.; Pour, S. Z.; Moll, G.; Catar, R.; Lavi, Y. B.; Silverberg, J. I.; Zimmerman, J.; Miranda, G. C. d.; Carvalho, R. F.; Khan, T. A.; Heidecke, H.; Dalmolin, R. J.; Luchessi, A. D.; Ochs, H. D.; Schimke, L. F.; Amital, H.; Riemekasten, G.; Zyskind, I.; Rosenberg, A. Z.; Vojdani, A.; Shoenfeld, Y.; Cabral-Marques, O.

2022-12-05 infectious diseases
10.1101/2022.12.04.22282902 medRxiv
Show abstract

Age is a significant risk factor for the coronavirus disease 2019 (COVID-19) outcomes due to immunosenescence and certain age-dependent medical conditions (e.g., obesity, cardiovascular disorder, diabetes, chronic respiratory disease). However, despite the well-known influence of age on autoantibody biology in health & disease, its impact on the risk of developing severe COVID-19 remains poorly explored. Here, we performed a cross-sectional study of autoantibodies directed against 58 targets associated with autoimmune diseases in 159 individuals with different COVID-19 outcomes (with 71 mild, 61 moderate, and 27 severe patients) and 73 healthy controls. We found that the natural production of autoantibodies increases with age and is exacerbated by SARS-CoV-2 infection, mostly in severe COVID-19 patients. Multivariate regression analysis showed that severe COVID-19 patients have a significant age-associated increase of autoantibody levels against 16 targets (e.g., amyloid {beta} peptide, {beta} catenin, cardiolipin, claudin, enteric nerve, fibulin, insulin receptor a, and platelet glycoprotein). Principal component analysis with spectrum decomposition based on these autoantibodies indicated an age-dependent stratification of severe COVID-19 patients. Random forest analysis ranked autoantibodies targeting cardiolipin, claudin, and platelet glycoprotein as the three most crucial autoantibodies for the stratification of severe elderly COVID-19 patients. Follow-up analysis using binomial regression found that anti-cardiolipin and anti-platelet glycoprotein autoantibodies indicated a significantly increased likelihood of developing a severe COVID-19 phenotype, presenting a synergistic effect on worsening COVID-19 outcomes. These findings provide new key insights to explain why elderly patients less favorable outcomes have than young individuals, suggesting new associations of distinct autoantibody levels with disease severity.

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