Evidence map›Paper›PMID 36703980›Full record

Trial reportFrontiers in immunology2022

Persistence of salivary antibody responses after COVID-19 vaccination is associated with oral microbiome variation in both healthy and people living with HIV.

Mahin Ghorbani, Khaled Al-Manei, Sabrina Naud, Katie Healy, Giorgio Gabarrini, Michal Jacek Sobkowiak, Puran Chen, Shilpa Ray, Mira Akber, Sandra Muschiol and 9 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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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

19 authors at 4 institutions in 2 countries.

Mahin GhorbaniDepartment of Dental Medicine, Karolinska Institutet, Huddinge, Sweden.
Khaled Al-ManeiDepartment of Dental Medicine, Karolinska Institutet, Huddinge, Sweden.
Sabrina NaudDepartment of Dental Medicine, Karolinska Institutet, Huddinge, Sweden.
Katie HealyDepartment of Dental Medicine, Karolinska Institutet, Huddinge, Sweden.
Giorgio GabarriniDepartment of Dental Medicine, Karolinska Institutet, Huddinge, Sweden.
Michal Jacek SobkowiakDepartment of Dental Medicine, Karolinska Institutet, Huddinge, Sweden.
Puran ChenDepartment of Medicine, Huddinge, Karolinska Institutet, Huddinge, Sweden.
Shilpa RayDepartment of Laboratory Medicine, Karolinska Institutet, Huddinge, Sweden.
Mira AkberDepartment of Medicine, Huddinge, Karolinska Institutet, Huddinge, Sweden.
Sandra MuschiolDepartment of Clinical Microbiology, Karolinska University Hospital, Stockholm, Sweden.
Gordana BogdanovicDepartment of Clinical Microbiology, Karolinska University Hospital, Stockholm, Sweden.
Peter BergmanDepartment of Laboratory Medicine, Karolinska Institutet, Huddinge, Sweden.
Per LjungmanDepartment of Medicine, Huddinge, Karolinska Institutet, Huddinge, Sweden.
Marcus BuggertDepartment of Medicine, Huddinge, Karolinska Institutet, Huddinge, Sweden.
Hans-Gustaf LjunggrenDepartment of Medicine, Huddinge, Karolinska Institutet, Huddinge, Sweden.
Elisa PinDepartment of Protein Science, SciLifeLab, KTH Royal Institute of Technology, Stockholm, Sweden.
Piotr NowakDepartment of Medicine, Huddinge, Karolinska Institutet, Huddinge, Sweden.
Soo AlemanDepartment of Medicine, Huddinge, Karolinska Institutet, Huddinge, Sweden.
Margaret Sällberg ChenDepartment of Dental Medicine, Karolinska Institutet, Huddinge, Sweden.
Karolinska Institutet · SEKarolinska University Hospital · SEKing Saud University · SAKTH Royal Institute of Technology · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coevolution of microbiome and immunity at mucosal sites is essential for our health. Whether the oral microbiome, the second largest community after the gut, contributes to the immunogenicity of COVID-19 vaccines is not known. We investigated the baseline oral microbiome in individuals in the COVAXID clinical trial receiving the BNT162b2 mRNA vaccine. Participants (n=115) included healthy controls (HC; n=57) and people living with HIV (PLHIV; n=58) who met the study selection criteria. Vaccine-induced Spike antibodies in saliva and serum from 0 to 6 months were assessed and comparative analyses were performed against the individual salivary 16S ASV microbiome diversity. High- versus low vaccine responders were assessed on general, immunological, and oral microbiome features. Our analyses identified oral microbiome features enriched in high-

Indexed as

BNT162 VaccineCOVID-19Antibodies, ViralAntibody FormationHIV InfectionsHumansImmunoglobulin A, SecretorySalivaAntibodies, ViralBNT162 VaccineImmunoglobulin A, SecretorycampylobactergemellagranulicatellaleptotrichiamRNA vaccinationOral microbiomesalivaSARS-CoV-2

Identifiers

PMID36703980
PMCPMC9871925
OpenAlexW4315471619

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.