English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/216781
Share/Impact:
Statistics
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE
Exportar a otros formatos:

Title

The antibody response to the glycan α-Gal correlates with COVID-19 disease symptoms

AuthorsUrra, José Miguel; Ferreras-Colino, Elisa; Contreras, Marinela; Cabrera, Carmen M.; Fernández de Mera, Isabel G.; Villar, Margarita ; Cabezas-Cruz, Alejandro; Gortázar, Christian ; Fuente, José de la
Issue Date14-Jul-2020
PublisherBioRxiv
AbstractThe coronavirus disease 19 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has affected millions of people worldwide. The characterization of the immunological mechanisms involved in disease symptomatology and protective response is important to advance in disease control and prevention. Humans evolved by losing the capacity to synthesize the glycan Galα1-3Galβ1-(3)4GlcNAc-R (α-Gal), which resulted in the development of a protective response against pathogenic viruses and other microorganisms containing this modification on membrane proteins mediated by anti-α-Gal IgM/IgG antibodies produced in response to bacterial microbiota. In addition to anti-α-Gal antibody-mediated pathogen opsonization, this glycan induces various immune mechanisms that have shown protection in animal models against infectious diseases without inflammatory responses. In this study, we hypothesized that the immune response to α-Gal may contribute to the control of COVID-19. To address this hypothesis, we characterized the antibody response to α-Gal in patients at different stages of COVID-19 and in comparison with healthy control individuals. The results showed that while the inflammatory response and the anti-SARS-CoV-2 (Spike) IgG antibody titers increased, reduction in anti-α-Gal IgE, IgM and IgG antibody titers and alteration of anti-α-Gal antibody isotype composition correlated with COVID-19 severity. The results suggested that the inhibition of the α-Gal-induced immune response may translate into more aggressive viremia and severe disease inflammatory symptoms. These results support the proposal of developing interventions such as probiotics based on commensal bacteria with α-Gal epitopes to modify the microbiota and increase the α-Gal-induced protective immune response and reduce the severity of COVID-19.
Publisher version (URL)https://doi.org/10.1101/2020.07.14.201954
URIhttp://hdl.handle.net/10261/216781
DOIhttp://dx.doi.org/10.1101/2020.07.14.201954
Appears in Collections:(IREC) Artículos
(VICYT) Colección Especial COVID-19
Files in This Item:
File Description SizeFormat 
The antibody response_Urra.pdf1 MBAdobe PDFThumbnail
View/Open
Show full item record
Review this work
 


WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.