Neutralizing Antibody Response of Vaccinees to SARS-CoV-2 Variants.

SARS-CoV-2 neutralizing antibody vaccine variants

Journal

Vaccines
ISSN: 2076-393X
Titre abrégé: Vaccines (Basel)
Pays: Switzerland
ID NLM: 101629355

Informations de publication

Date de publication:
18 May 2021
Historique:
received: 20 04 2021
revised: 14 05 2021
accepted: 16 05 2021
entrez: 2 6 2021
pubmed: 3 6 2021
medline: 3 6 2021
Statut: epublish

Résumé

Due to their increased transmissibility, three variants of high concern have emerged in the United Kingdom (also known as B.1.1.7 lineage or VOC-202012/01), South Africa (B.1.351 lineage), and Brazil (P1 lineage) with multiple substitutions in the spike protein. Since neutralizing antibodies elicited by vaccination are likely considered as correlates of protection for SARS-CoV-2 infection, it is important to analyze whether vaccinees with mRNA BNT162b2 are equally protected against these emerging SARS-CoV-2 variants. To this aim, we enrolled healthy subjects one month after complete vaccination with Comirnaty and evaluated the neutralizing response against the native Wuhan strain and the emerging B.1.1.7, B.1.351 and P1 lineages, by using the microneutralization assay, currently considered the gold standard test for the evaluation and detection of functional neutralizing antibodies. The most remarkable finding of this study was the significantly lower neutralizing antibody titer against B.1.351 lineage, compared to the wild-type virus. No significant differences were observed with the other two lineages. These findings provide evidence that vaccinated subjects may not be equally protected against all SARS-CoV-2 lineages.

Identifiants

pubmed: 34069852
pii: vaccines9050517
doi: 10.3390/vaccines9050517
pmc: PMC8157345
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Gabriele Anichini (G)

Virology Unit, Department of Medical Biotechnologies, Siena University Hospital, 53100 Siena, Italy.

Chiara Terrosi (C)

Virology Unit, Department of Medical Biotechnologies, Siena University Hospital, 53100 Siena, Italy.

Gianni Gori Savellini (G)

Virology Unit, Department of Medical Biotechnologies, Siena University Hospital, 53100 Siena, Italy.

Claudia Gandolfo (C)

Virology Unit, Department of Medical Biotechnologies, Siena University Hospital, 53100 Siena, Italy.

Federico Franchi (F)

Emergency, Anesthesia and Intensive Care Unit, Department of Medicine, Surgery and Neurosciences, Siena University Hospital, 53100 Siena, Italy.

Maria Grazia Cusi (MG)

Virology Unit, Department of Medical Biotechnologies, Siena University Hospital, 53100 Siena, Italy.

Classifications MeSH