Immune response to SARS-CoV-2 Omicron variant in patients and vaccinees following homologous and heterologous vaccinations.


Journal

Communications biology
ISSN: 2399-3642
Titre abrégé: Commun Biol
Pays: England
ID NLM: 101719179

Informations de publication

Date de publication:
02 09 2022
Historique:
received: 06 02 2022
accepted: 16 08 2022
entrez: 2 9 2022
pubmed: 3 9 2022
medline: 9 9 2022
Statut: epublish

Résumé

The SARS-CoV-2 Omicron variant has rapidly replaced the Delta variant of concern. This new variant harbors worrisome mutations on the spike protein, which are able to escape the immunity elicited by vaccination and/or natural infection. To evaluate the impact and susceptibility of different serum samples to the Omicron variant BA.1, samples from COVID-19 patients and vaccinated individuals were tested for their ability to bind and neutralize the original SARS-CoV-2 virus and the Omicron variant BA.1. COVID-19 patients show the most drastic reduction in Omicron-specific antibody response in comparison with the response to the wild-type virus. Antibodies elicited by a triple homologous/heterologous vaccination regimen or following natural SARS-CoV-2 infection combined with a two-dose vaccine course, result in highest neutralization capacity against the Omicron variant BA.1. Overall, these findings confirm that vaccination of COVID-19 survivors and booster dose to vaccinees with mRNA vaccines is the correct strategy to enhance the antibody cross-protection against Omicron variant BA.1.

Identifiants

pubmed: 36056181
doi: 10.1038/s42003-022-03849-0
pii: 10.1038/s42003-022-03849-0
pmc: PMC9439265
doi:

Substances chimiques

Membrane Glycoproteins 0
Spike Glycoprotein, Coronavirus 0
Viral Envelope Proteins 0
spike protein, SARS-CoV-2 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

903

Informations de copyright

© 2022. The Author(s).

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Auteurs

Claudia Maria Trombetta (CM)

Department of Molecular and Developmental Medicine, University of Siena, Siena, Italy. trombetta@unisi.it.

Giulia Piccini (G)

VisMederi srl, Siena, Italy.

Margherita Leonardi (M)

VisMederi Research srl, Siena, Italy.

Francesca Dapporto (F)

VisMederi Research srl, Siena, Italy.

Serena Marchi (S)

Department of Molecular and Developmental Medicine, University of Siena, Siena, Italy.

Emanuele Andreano (E)

Monoclonal Antibody Discovery (MAD) Lab, Fondazione Toscana Life Sciences, Siena, Italy.

Ida Paciello (I)

Monoclonal Antibody Discovery (MAD) Lab, Fondazione Toscana Life Sciences, Siena, Italy.

Linda Benincasa (L)

VisMederi Research srl, Siena, Italy.

Piero Lovreglio (P)

Interdisciplinary Department of Medicine, Section of Occupational Medicine, University of Bari, Bari, Italy.

Nicola Buonvino (N)

U.O.C. Penitentiary Medicine-Department of Territorial Care, Bari Local Health Authority, Bari, Italy.

Nicola Decaro (N)

Department of Veterinary Medicine, University of Bari, Bari, Italy.

Angela Stufano (A)

Interdisciplinary Department of Medicine, Section of Occupational Medicine, University of Bari, Bari, Italy.

Eleonora Lorusso (E)

Department of Veterinary Medicine, University of Bari, Bari, Italy.

Emilio Bombardieri (E)

Humanitas Gavazzeni, Bergamo, Italy.

Antonella Ruello (A)

Humanitas Gavazzeni, Bergamo, Italy.

Simonetta Viviani (S)

Department of Molecular and Developmental Medicine, University of Siena, Siena, Italy.

Rino Rappuoli (R)

Monoclonal Antibody Discovery (MAD) Lab, Fondazione Toscana Life Sciences, Siena, Italy.
Department of Biotechnology, Chemistry and Pharmacy, University of Siena, Siena, Italy.

Eleonora Molesti (E)

VisMederi Research srl, Siena, Italy.

Alessandro Manenti (A)

VisMederi srl, Siena, Italy.

Emanuele Montomoli (E)

Department of Molecular and Developmental Medicine, University of Siena, Siena, Italy.
VisMederi srl, Siena, Italy.
VisMederi Research srl, Siena, Italy.

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Classifications MeSH