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Single-reaction multi-antigen serological test for comprehensive evaluation of SARS-CoV-2 patients by flow cytometry

Authors :
Consejo Superior de Investigaciones Científicas (España)
Comunidad de Madrid
Ministerio de Ciencia, Innovación y Universidades (España)
Agencia Estatal de Investigación (España)
European Commission
Instituto de Salud Carlos III
Fundación la Caixa
Banco Santander
Conferencia de Rectores de las Universidades Españolas
Valés-Gómez, Mar [0000-0001-7424-3206]
Cáceres-Martell, Yaiza
Fernández-Soto, Daniel
Campos-Silva, Carmen
García-Cuesta, Eva María
Casasnovas, José María
Navas-Herrera, David
Beneítez-Martínez, Alexandra
Martinez-Fleta, Pedro
Alfranca, Arántzazu
Sánchez-Madrid, Francisco
Escudero López, Gabriela
Vilches, Carlos
Jara-Acevedo, Ricardo
Reyburn, H. T.
Rodríguez-Frade, José Miguel
Valés-Gómez, Mar
Consejo Superior de Investigaciones Científicas (España)
Comunidad de Madrid
Ministerio de Ciencia, Innovación y Universidades (España)
Agencia Estatal de Investigación (España)
European Commission
Instituto de Salud Carlos III
Fundación la Caixa
Banco Santander
Conferencia de Rectores de las Universidades Españolas
Valés-Gómez, Mar [0000-0001-7424-3206]
Cáceres-Martell, Yaiza
Fernández-Soto, Daniel
Campos-Silva, Carmen
García-Cuesta, Eva María
Casasnovas, José María
Navas-Herrera, David
Beneítez-Martínez, Alexandra
Martinez-Fleta, Pedro
Alfranca, Arántzazu
Sánchez-Madrid, Francisco
Escudero López, Gabriela
Vilches, Carlos
Jara-Acevedo, Ricardo
Reyburn, H. T.
Rodríguez-Frade, José Miguel
Valés-Gómez, Mar
Publication Year :
2021

Abstract

Here, we describe a new, simple, highly multiplexed serological test that generates a more complete picture of seroconversion than single antigen-based assays. Flow cytometry is used to detect multiple Ig isotypes binding to four SARS-CoV-2 antigens: the Spike glycoprotein, its RBD fragment (the main target for neutralizing antibodies), the nucleocapsid protein, and the main cysteine-like protease in a single reaction. Until now, most diagnostic serological tests measured antibodies to only one antigen and in some laboratory-confirmed patients no SARS-CoV-2-specific antibodies could be detected. Our data reveal that while most patients respond against all the viral antigens tested, others show a marked bias to make antibodies against either proteins exposed on the viral particle or those released after cellular infection. With this assay, it was possible to discriminate between patients and healthy controls with 100% confidence. Analysing the response of multiple Ig isotypes to the four antigens in combination may also help to establish a correlation with the severity degree of disease. A more detailed description of the immune responses of different patients to SARS-CoV-2 virus might provide insight into the wide array of clinical presentations of COVID-19.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1286580905
Document Type :
Electronic Resource