Abnormal antibodies to self-carbohydrates in SARS-CoV-2-infected patients

Author:

Butler Dorothy L1,Imberti Luisa2,Quaresima Virginia2,Fiorini Chiara2,Barnett Jason,Chauvin Samuel,Cheng Xi,Danielson Jeffrey,Dobbs Kerry,Garabedian Elizabeth,Kuram Vasu,Lau William,Li Zhiwen,Magliocco Mary,Matthews Helen,Nambiar Marshall,Samuel Smilee,Shaw Elana,Stack Michael,Weber Sarah,Xirasagar Sandhya,Zhang Yu,Gildersleeve Jeffrey C1,

Affiliation:

1. Chemical Biology Laboratory, Center for Cancer Research, National Cancer Institute , Frederick, MD 21702, USA

2. Centro di Ricerca Emato-oncologica AIL (CREA) and Diagnostic Department, ASST Spedali Civili di Brescia , Brescia, Italy

Abstract

Abstract Our immune system is critical for preventing and treating SARS-CoV-2 infections, but aberrant immune responses can have deleterious effects. While antibodies to glycans could recognize the virus and influence the clinical outcome, little is known about their roles. Using a carbohydrate antigen microarray, we profiled serum antibodies in healthy control subjects and COVID-19 patients from two separate cohorts. COVID-19 patients had numerous autoantibodies to self-glycans, including antiganglioside antibodies that can cause neurological disorders. Additionally, nearly all antiglycan IgM signals were lower in COVID-19 patients, indicating a global dysregulation of this class of antibodies. Autoantibodies to certain N-linked glycans correlated with more severe disease, as did low levels of antibodies to the Forssman antigen and ovalbumin. Collectively, this study indicates that expanded testing for antiglycan antibodies could be beneficial for clinical analysis of COVID-19 patients and illustrates the importance of including host and viral carbohydrate antigens when studying immune responses to viruses.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

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