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Description of SARS-CoV-2 T-cell polyfunctionality features

Authors :
Pérez-Gómez, Alberto
Gasca-Capote, María del Carmen
Vitallé, Joana
Ostos, Francisco José
Serna, Ana
Trujillo-Rodríguez, María
Muñoz-Muela, Esperanza
Giráldez-Pérez, Teresa
Praena-Segovia, Julia
Navarro-Amuedo, María Dolores
Paniagua-García, María
García-Gutiérrez, Manuel
Aguilar Guisado, Manuela
Rivas-Jeremías, Inmaculada
Jiménez-León, María Reyes
Bachiller, Sara
Fernández-Villar, Alberto
Pérez-González, Alexandre
Gutiérrez-Valencia, Alicia
Rafii-El-Idrissi Benhnia, Mohamed
Weiskopf, Daniela
Sette, Alessandro
López-Cortés, Luis F.
Poveda, Eva
Ruiz-Mateos, Ezequiel
Virgen del Rocío Hospital COVID-19 Working Team
COHVID-GS Working Team
Junta de Andalucía
National Institutes of Health (US)
Instituto de Salud Carlos III
Red Española de Investigación en SIDA
European Commission
Consejo Superior de Investigaciones Científicas (España)
Pérez-Gómez, Alberto
Pérez-González, Alexandre
Pérez-Gómez, Alberto [0000-0002-3644-2914]
Pérez-González, Alexandre [0000-0003-4836-6768]
Source :
Digital.CSIC. Repositorio Institucional del CSIC, instname
Publication Year :
2021
Publisher :
BioRxiv, 2021.

Abstract

SARS-CoV-2 specific T-cell response has been associated with disease severity, immune memory and heterologous response to endemic coronaviruses. However, an integrative approach combining a comprehensive analysis of the quality of SARS-CoV-2 specific T-cell response with antibody levels in these three scenarios is needed. In the present study we found that, in acute infection, while mild disease was associated with high T-cell polyfunctionality biased to IL-2 production and inversely correlated with anti-S IgG levels, combinations only including IFN-gamma; with absence of perforin production predominated in severe disease. Seven months after infection, both non-hospitalized and previously hospitalized patients presented robust anti-S IgG levels and SARS-CoV-2 specific T-cell response. In addition, only previously hospitalized patients showed a T-cell exhaustion profile. Finally, combinations including IL-2 in response to S protein of endemic coronaviruses, were the ones associated with SARS-CoV-2 S-specific T-cell response in pre-COVID-19 samples from healthy donors. These results have implications for protective immunity against SARS-CoV-2 and recurrent COVID-19 and may help for the design of new prototypes and boosting vaccine strategies.<br />Consejeria de Transformacion Economica, Industria, Conocimiento y Universidades Junta de Andalucia (research Project CV20-85418) (ERM) NIH contract 75N9301900065 (AS, DW) Consejeria de Salud Junta de Andalucia (Research Contract RH-0037-2020 to JV) Instituto de Salud Carlos III (CP19/00159 to AGV, FI17/00186 to MRJL, FI19/00083 to CGC, CM20/00243 to APG and COV20/00698 to support COHVID-GS) Red Temática de Investigación Cooperativa en SIDA (RD16/0025/0020; RD16/0025/0026), which is included in the Acción Estratégica en Salud, Plan Nacional de Investigación Científica, Desarrollo e Innovación Tecnológica, 2008 to 2011 and 2013 to 2016 Instituto de Salud Carlos III, Fondos FEDER. ERM was supported by the Spanish Research Council (CSIC). “Contratación de Personal Investigador Doctor” supported by the European Social Fund and Junta de Andalucía (PAIDI DOCTOR- Convocatoria 2019-2020). (FJO, SB).

Details

Language :
English
Database :
OpenAIRE
Journal :
Digital.CSIC. Repositorio Institucional del CSIC, instname
Accession number :
edsair.dedup.wf.001..28f280407a711b5407969502baa123d7