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Cross-Sectional Evaluation of Humoral Responses against SARS-CoV-2 Spike

Authors :
Jérémie Prévost
Romain Gasser
Guillaume Beaudoin-Bussières
Jonathan Richard
Ralf Duerr
Annemarie Laumaea
Sai Priya Anand
Guillaume Goyette
Mehdi Benlarbi
Shilei Ding
Halima Medjahed
Antoine Lewin
Josée Perreault
Tony Tremblay
Gabrielle Gendron-Lepage
Nicolas Gauthier
Marc Carrier
Diane Marcoux
Alain Piché
Myriam Lavoie
Alexandre Benoit
Vilayvong Loungnarath
Gino Brochu
Elie Haddad
Hannah D. Stacey
Matthew S. Miller
Marc Desforges
Pierre J. Talbot
Graham T. Gould Maule
Marceline Côté
Christian Therrien
Bouchra Serhir
Renée Bazin
Michel Roger
Andrés Finzi
Source :
Cell Reports Medicine, Vol 1, Iss 7, Pp 100126- (2020)
Publication Year :
2020
Publisher :
Elsevier, 2020.

Abstract

Summary: SARS-CoV-2 is responsible for the coronavirus disease 2019 (COVID-19) pandemic, infecting millions of people and causing hundreds of thousands of deaths. The Spike glycoproteins of SARS-CoV-2 mediate viral entry and are the main targets for neutralizing antibodies. Understanding the antibody response directed against SARS-CoV-2 is crucial for the development of vaccine, therapeutic, and public health interventions. Here, we perform a cross-sectional study on 106 SARS-CoV-2-infected individuals to evaluate humoral responses against SARS-CoV-2 Spike. Most infected individuals elicit anti-Spike antibodies within 2 weeks of the onset of symptoms. The levels of receptor binding domain (RBD)-specific immunoglobulin G (IgG) persist over time, and the levels of anti-RBD IgM decrease after symptom resolution. Although most individuals develop neutralizing antibodies within 2 weeks of infection, the level of neutralizing activity is significantly decreased over time. Our results highlight the importance of studying the persistence of neutralizing activity upon natural SARS-CoV-2 infection.

Details

Language :
English
ISSN :
26663791
Volume :
1
Issue :
7
Database :
Directory of Open Access Journals
Journal :
Cell Reports Medicine
Publication Type :
Academic Journal
Accession number :
edsdoj.f77f34cf5d734e3f9175ba9330620ffe
Document Type :
article
Full Text :
https://doi.org/10.1016/j.xcrm.2020.100126