Mucosal immune response after the booster dose of the BNT162b2 COVID-19 vaccine.


Journal

EBioMedicine
ISSN: 2352-3964
Titre abrégé: EBioMedicine
Pays: Netherlands
ID NLM: 101647039

Informations de publication

Date de publication:
Feb 2023
Historique:
received: 07 06 2022
revised: 21 12 2022
accepted: 23 12 2022
pubmed: 12 1 2023
medline: 15 2 2023
entrez: 11 1 2023
Statut: ppublish

Résumé

To date, only a few studies reported data regarding the development of mucosal immune response after the BNT162b2-booster vaccination. Samples of both serum and saliva of 50 healthcare workers were collected at the day of the booster dose (T3) and after two weeks (T4). Anti-S1-protein IgG and IgA antibody titres and the neutralizing antibodies against the Wuhan wild-type Receptor-Binding Domain in both serum and saliva were measured by quantitative and competitive ELISA, respectively. Data were compared with those recorded after the primary vaccination cycle (T2). Neutralizing antibodies against the variants of concern were measured in those individuals with anti-Wuhan neutralizing antibodies in their saliva. After eight months from the second dose, IgG decreased in both serum (T2 The BNT162b2-booster vaccination elicits a strong systemic immune response but fails in activating an effective mucosal immunity against the Omicron BA.1 variant. This work was funded by the Department of Medicine and Surgery, University of Insubria, and supported by Fondazione Umberto Veronesi (COVID-19 Insieme per la ricerca di tutti, 2020), Italy.

Sections du résumé

BACKGROUND BACKGROUND
To date, only a few studies reported data regarding the development of mucosal immune response after the BNT162b2-booster vaccination.
METHODS METHODS
Samples of both serum and saliva of 50 healthcare workers were collected at the day of the booster dose (T3) and after two weeks (T4). Anti-S1-protein IgG and IgA antibody titres and the neutralizing antibodies against the Wuhan wild-type Receptor-Binding Domain in both serum and saliva were measured by quantitative and competitive ELISA, respectively. Data were compared with those recorded after the primary vaccination cycle (T2). Neutralizing antibodies against the variants of concern were measured in those individuals with anti-Wuhan neutralizing antibodies in their saliva.
FINDINGS RESULTS
After eight months from the second dose, IgG decreased in both serum (T2
INTERPRETATION CONCLUSIONS
The BNT162b2-booster vaccination elicits a strong systemic immune response but fails in activating an effective mucosal immunity against the Omicron BA.1 variant.
FUNDING BACKGROUND
This work was funded by the Department of Medicine and Surgery, University of Insubria, and supported by Fondazione Umberto Veronesi (COVID-19 Insieme per la ricerca di tutti, 2020), Italy.

Identifiants

pubmed: 36628844
pii: S2352-3964(22)00617-X
doi: 10.1016/j.ebiom.2022.104435
pmc: PMC9828819
pii:
doi:

Substances chimiques

BNT162 Vaccine 0
COVID-19 Vaccines 0
Antibodies, Neutralizing 0
Immunoglobulin A 0
Immunoglobulin G 0
Antibodies, Viral 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104435

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests None to declare.

Auteurs

Lorenzo Azzi (L)

Azienda Socio-Sanitaria Territoriale dei Sette Laghi, Department of Medicine and Surgery, University of Insubria, Varese, Italy.

Daniela Dalla Gasperina (D)

Azienda Socio-Sanitaria Territoriale dei Sette Laghi, Department of Medicine and Surgery, University of Insubria, Varese, Italy.

Giovanni Veronesi (G)

Research Centre in Epidemiology and Preventive Medicine (EPIMED), Department of Medicine and Surgery, University of Insubria, Varese, Italy.

Mariam Shallak (M)

Laboratory of General Pathology and Immunology "Giovanna Tosi", Department of Medicine and Surgery, University of Insubria, Varese, Italy.

Vittorio Maurino (V)

Azienda Socio-Sanitaria Territoriale dei Sette Laghi, Department of Biotechnologies and Life Sciences, University of Insubria, Varese, Italy.

Andreina Baj (A)

Azienda Socio-Sanitaria Territoriale dei Sette Laghi, Department of Medicine and Surgery, University of Insubria, Varese, Italy.

Francesco Gianfagna (F)

Research Centre in Epidemiology and Preventive Medicine (EPIMED), Department of Medicine and Surgery, University of Insubria, Varese, Italy; Mediterranea Cardiocentro, Naples, Italy.

Pierpaolo Cavallo (P)

Department of Physics, University of Salerno, Fisciano (SA), Italy; Institute for Complex Systems, National Research Council, Rome, Italy.

Francesco Dentali (F)

Azienda Socio-Sanitaria Territoriale dei Sette Laghi, Department of Medicine and Surgery, University of Insubria, Varese, Italy.

Lucia Tettamanti (L)

Azienda Socio-Sanitaria Territoriale dei Sette Laghi, Department of Biotechnologies and Life Sciences, University of Insubria, Varese, Italy.

Fabrizio Maggi (F)

Azienda Socio-Sanitaria Territoriale dei Sette Laghi, Department of Medicine and Surgery, University of Insubria, Varese, Italy.

Lorenzo Stefano Maffioli (LS)

Chief Medical Officer, Azienda Socio-Sanitaria Territoriale dei Sette Laghi, Varese, Italy.

Angelo Tagliabue (A)

Azienda Socio-Sanitaria Territoriale dei Sette Laghi, Department of Medicine and Surgery, University of Insubria, Varese, Italy.

Roberto Sergio Accolla (RS)

Laboratory of General Pathology and Immunology "Giovanna Tosi", Department of Medicine and Surgery, University of Insubria, Varese, Italy.

Greta Forlani (G)

Laboratory of General Pathology and Immunology "Giovanna Tosi", Department of Medicine and Surgery, University of Insubria, Varese, Italy. Electronic address: greta.forlani@uninsubria.it.

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Classifications MeSH