Evidence map›Paper›PMID 33758842›Full record

ArticlebioRxiv : the preprint server for biology2021

Antibody responses to SARS-CoV-2 mRNA vaccines are detectable in saliva.

Thomas J Ketas, Devidas Chaturbhuj, Victor M Cruz-Portillo, Erik Francomano, Encouse Golden, Sharanya Chandrasekhar, Gargi Debnath, Randy Diaz-Tapia, Anila Yasmeen, Wilhem Leconet and 8 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed, 34 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 2 institutions in 2 countries.

Thomas J KetasDepartment of Microbiology and Immunology, Weill Cornell Medicine, New York, NY 10065.
Devidas ChaturbhujDepartment of Microbiology and Immunology, Weill Cornell Medicine, New York, NY 10065.
Victor M Cruz-PortilloDepartment of Microbiology and Immunology, Weill Cornell Medicine, New York, NY 10065.
Erik FrancomanoDepartment of Microbiology and Immunology, Weill Cornell Medicine, New York, NY 10065.
Encouse GoldenDepartment of Radiation Oncology, Weill Cornell Medicine, New York, NY 10065.
Sharanya ChandrasekharDepartment of Radiation Oncology, Weill Cornell Medicine, New York, NY 10065.
Gargi DebnathDepartment of Microbiology and Immunology, Weill Cornell Medicine, New York, NY 10065.
Randy Diaz-TapiaDepartment of Microbiology and Immunology, Weill Cornell Medicine, New York, NY 10065.
Anila YasmeenDepartment of Microbiology and Immunology, Weill Cornell Medicine, New York, NY 10065.
Wilhem LeconetDepartment of Urology, Weill Cornell Medicine, New York, NY 10065.
Zhen ZhaoDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY 10065.
Philip J M BrouwerDepartment of Medical Microbiology and Infection Prevention, Amsterdam University Medical Centers, Location AMC, University of Amsterdam, Amsterdam Infection & Immunity Institute, 1105 AZ Amsterdam, the Netherlands.
Melissa M CushingDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY 10065.
Rogier W SandersDepartment of Microbiology and Immunology, Weill Cornell Medicine, New York, NY 10065.
Albert CupoDepartment of Microbiology and Immunology, Weill Cornell Medicine, New York, NY 10065.
P J KlasseDepartment of Microbiology and Immunology, Weill Cornell Medicine, New York, NY 10065.
Silvia C FormentiDepartment of Radiation Oncology, Weill Cornell Medicine, New York, NY 10065.
John P MooreDepartment of Microbiology and Immunology, Weill Cornell Medicine, New York, NY 10065.
Cornell University · USAmsterdam University Medical Centers · NL

Funding

Neutralization of Primate Immunodeficiency VirusesR01AI036082 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI JOHN P MOORE · 1994 to 2026
$4.3M
Genetic protection of hematopoietic stem cells for stable HIV controlR01AI100652 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI AN, DONG SUNG · 2012 to 2016
$1.9M
NIAID NIH HHS R01 AI036082NIAID NIH HHS R01 AI100652
6 · The paper itself

Abstract

Vaccines are critical for curtailing the COVID-19 pandemic (1, 2). In the USA, two highly protective mRNA vaccines are available: BNT162b2 from Pfizer/BioNTech and mRNA-1273 from Moderna (3, 4). These vaccines induce antibodies to the SARS-CoV-2 S-protein, including neutralizing antibodies (NAbs) predominantly directed against the Receptor Binding Domain (RBD) (1-4). Serum NAbs are induced at modest levels within ~1 week of the first dose, but their titers are strongly boosted by a second dose at 3 (BNT162b2) or 4 weeks (mRNA-1273) (3, 4). SARS-CoV-2 is most commonly transmitted nasally or orally and infects cells in the mucosae of the respiratory and to some extent also the gastrointestinal tract (5). Although serum NAbs may be a correlate of protection against COVID-19, mucosal antibodies might directly prevent or limit virus acquisition by the nasal, oral and conjunctival routes (5). Whether the mRNA vaccines induce mucosal immunity has not been studied. Here, we report that antibodies to the S-protein and its RBD are present in saliva samples from mRNA-vaccinated healthcare workers (HCW). Within 1-2 weeks after their second dose, 37/37 and 8/8 recipients of the Pfizer and Moderna vaccines, respectively, had S-protein IgG antibodies in their saliva, while IgA was detected in a substantial proportion. These observations may be relevant to vaccine-mediated protection from SARS-CoV-2 infection and disease.

Indexed as

COVID-19RBDsalivaSARS-CoV-2S-protein

Identifiers

PMID33758842
PMCPMC7987001
OpenAlexW3133593904

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.