ELISA-Based Analysis Reveals an Anti-SARS-CoV-2 Protein Immune Response Profile Associated with Disease Severity.

COVID-19 SARS-CoV-2 antibodies SARS-CoV-2 linear epitopes disease severity

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
14 Jan 2022
Historique:
received: 14 12 2021
revised: 04 01 2022
accepted: 11 01 2022
entrez: 21 1 2022
pubmed: 22 1 2022
medline: 22 1 2022
Statut: epublish

Résumé

Since the start of the COVID-19 pandemic, many studies have investigated the humoral response to SARS-CoV-2 during infection. Studies with native viral proteins constitute a first-line approach to assessing the overall immune response, but small peptides are an accurate and valuable tool for the fine characterization of B-cell epitopes, despite the restriction of this approach to the determination of linear epitopes. In this study, we used ELISA and peptides covering a selection of structural and non-structural SARS-CoV-2 proteins to identify key epitopes eliciting a strong immune response that could serve as a biological signature of disease characteristics, such as severity, in particular. We used 213 plasma samples from a cohort of patients well-characterized clinically and biologically and followed for COVID-19 infection. We found that patients developing severe disease had higher titers of antibodies mapping to multiple specific epitopes than patients with mild to moderate disease. These data are potentially important as they could be used for immunological profiling to improve our knowledge of the quantitative and qualitative characteristics of the humoral response in relation to patient outcome.

Identifiants

pubmed: 35054099
pii: jcm11020405
doi: 10.3390/jcm11020405
pmc: PMC8781066
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Agence Nationale de la Recherche
ID : ANR-20-COVI-0011-01
Organisme : Centre Val de Loire
ID : 2020 00140687

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Auteurs

Charline Herrscher (C)

Inserm U1259 Morphogénèse et Antigénicité du VIH et des virus des Hépatites, Université de Tours et CHRU de Tours, 37000 Tours, France.

Sébastien Eymieux (S)

Inserm U1259 Morphogénèse et Antigénicité du VIH et des virus des Hépatites, Université de Tours et CHRU de Tours, 37000 Tours, France.

Christophe Gaborit (C)

Epidémiologie des Données Cliniques en Centre-Val de Loire (EpiDcliC), Centre Hospitalier Universitaire de Tours, 37000 Tours, France.

Hélène Blasco (H)

Service de Biochimie et Biologie Moléculaire, CHRU de Tours, 37000 Tours, France.

Julien Marlet (J)

Inserm U1259 Morphogénèse et Antigénicité du VIH et des virus des Hépatites, Université de Tours et CHRU de Tours, 37000 Tours, France.
Service de Bactériologie-Virologie-Hygiène, CHRU de Tours, 37000 Tours, France.

Karl Stefic (K)

Inserm U1259 Morphogénèse et Antigénicité du VIH et des virus des Hépatites, Université de Tours et CHRU de Tours, 37000 Tours, France.
Service de Bactériologie-Virologie-Hygiène, CHRU de Tours, 37000 Tours, France.

Philippe Roingeard (P)

Inserm U1259 Morphogénèse et Antigénicité du VIH et des virus des Hépatites, Université de Tours et CHRU de Tours, 37000 Tours, France.

Leslie Grammatico-Guillon (L)

Inserm U1259 Morphogénèse et Antigénicité du VIH et des virus des Hépatites, Université de Tours et CHRU de Tours, 37000 Tours, France.
Epidémiologie des Données Cliniques en Centre-Val de Loire (EpiDcliC), Centre Hospitalier Universitaire de Tours, 37000 Tours, France.

Christophe Hourioux (C)

Inserm U1259 Morphogénèse et Antigénicité du VIH et des virus des Hépatites, Université de Tours et CHRU de Tours, 37000 Tours, France.

Classifications MeSH