Evidence map›Paper›PMID 35393790›Full record

ArticleEMBO molecular medicine2022

BNT162b2 vaccine induces antibody release in saliva: a possible role for mucosal viral protection?

Abbass Darwich, Chiara Pozzi, Giulia Fornasa, Michela Lizier, Elena Azzolini, Ilaria Spadoni, Francesco Carli, Antonio Voza, Antonio Desai, Carlo Ferrero and 4 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
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  7. SARS-CoV-2-specific mucosal immune response in vaccinated versus infected children.Frontiers in cellular and infection microbiology · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 2 countries.

Abbass Darwich *Department of Biomedical Sciences, Humanitas University, Milan, Italy.
Chiara Pozzi *IRCCS Humanitas Research Hospital, Milan, Italy.ORCID 0000-0003-2153-6130
Giulia FornasaIRCCS Humanitas Research Hospital, Milan, Italy.ORCID 0000-0002-2250-7983
Michela LizierIRCCS Humanitas Research Hospital, Milan, Italy.ORCID 0000-0002-3173-5793
Elena AzzoliniDepartment of Biomedical Sciences, Humanitas University, Milan, Italy.
Ilaria SpadoniDepartment of Biomedical Sciences, Humanitas University, Milan, Italy.
Francesco CarliDepartment of Informatics, Università degli Studi di Torino, Torino, Italy.
Antonio VozaDepartment of Biomedical Sciences, Humanitas University, Milan, Italy.
Antonio DesaiDepartment of Biomedical Sciences, Humanitas University, Milan, Italy.ORCID 0000-0003-4674-4905
Carlo FerreroIRCCS Humanitas Research Hospital, Milan, Italy.ORCID 0000-0003-4332-5836
Luca GermagnoliIRCCS Humanitas Research Hospital, Milan, Italy.
ICH COVID-19 Task-force
Alberto MantovaniDepartment of Biomedical Sciences, Humanitas University, Milan, Italy.
Maria RescignoDepartment of Biomedical Sciences, Humanitas University, Milan, Italy.ORCID 0000-0002-6464-509X
Humanitas University · ITIRCCS Humanitas Research Hospital · ITUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vaccination against an airborne pathogen is very effective if it induces also the development of mucosal antibodies that can protect against infection. The mRNA-based vaccine-encoding SARS-CoV-2 full-length spike protein (BNT162b2, Pfizer/BioNTech) protects also against infection despite being administered systemically. Here, we show that upon vaccination, cognate IgG molecules are also found in the saliva and are more abundant in SARS-CoV-2 previously exposed subjects, paralleling the development of plasma IgG. The antibodies titer declines at 3 months from vaccination. We identified a concentration of specific IgG in the plasma above which the relevant IgG can be detected in the saliva. Regarding IgA antibodies, we found only protease-susceptible IgA1 antibodies in plasma while they were present at very low levels in the saliva over the course of vaccination of SARS-CoV-2-naïve subjects. Thus, in response to BNT162b2 vaccine, plasma IgG can permeate into mucosal sites and participate in viral protection. It is not clear why IgA1 are detected in low amount, they may be proteolytically cleaved.

Indexed as

COVID-19SARS-CoV-2Antibodies, ViralBNT162 VaccineCOVID-19 VaccinesHumansImmunoglobulin AImmunoglobulin GSalivaVaccinationAntibodies, ViralBNT162 VaccineCOVID-19 VaccinesImmunoglobulin AImmunoglobulin GBNT162b2IgAIgGmucosal immunitySARS-CoV-2

Identifiers

PMID35393790
PMCPMC9081904
OpenAlexW4224291430

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.