Evidence map›Paper›PMID 35871873›Full record

ArticleVaccine2022

Skin-patch delivered subunit vaccine induces broadly neutralising antibodies against SARS-CoV-2 variants of concern.

Christopher L D McMillan, Alberto A Amarilla, Naphak Modhiran, Jovin J Y Choo, Armira Azuar, Kate E Honeyman, Alexander A Khromykh, Paul R Young, Daniel Watterson, David A Muller

Open access · hybridAbstract read
In one paragraph

Article in Vaccine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

7 citing papers in PubMed, 17 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Christopher L D McMillanSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Queensland, Australia.
Alberto A AmarillaSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Queensland, Australia.
Naphak ModhiranSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Queensland, Australia.
Jovin J Y ChooSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Queensland, Australia.
Armira AzuarSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Queensland, Australia.
Kate E HoneymanSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Queensland, Australia.
Alexander A KhromykhSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Queensland, Australia.
Paul R YoungSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Queensland, Australia; Australian Infectious Diseases Research Centre, Global Virus Network Centre of Excellence, Brisbane, Queensland, Australia.
Daniel WattersonSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Queensland, Australia; Australian Infectious Diseases Research Centre, Global Virus Network Centre of Excellence, Brisbane, Queensland, Australia.
David A MullerSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Queensland, Australia; Australian Infectious Diseases Research Centre, Global Virus Network Centre of Excellence, Brisbane, Queensland, Australia. Electronic address: d.muller4@uq.edu.au.
University of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ongoing SARS-CoV-2 pandemic continues to pose an enormous health challenge globally. The ongoing emergence of variants of concern has resulted in decreased vaccine efficacy necessitating booster immunizations. This was particularly highlighted by the recent emergence of the Omicron variant, which contains over 30 mutations in the spike protein and quickly became the dominant viral strain in global circulation. We previously demonstrated that delivery of a SARS-CoV-2 subunit vaccine via a high-density microarray patch (HD-MAP) induced potent immunity resulting in robust protection from SARS-CoV-2 challenge in mice. Here we show that serum from HD-MAP immunized animals maintained potent neutralisation against all variants tested, including Delta and Omicron. These findings highlight the advantages of HD-MAP vaccine delivery in inducing high levels of neutralising antibodies and demonstrates its potential at providing protection from emerging viral variants.

Indexed as

COVID-19Viral VaccinesAnimalsAntibodies, NeutralizingAntibodies, ViralBroadly Neutralizing AntibodiesCOVID-19 VaccinesHumansMiceSARS-CoV-2Spike Glycoprotein, CoronavirusVaccines, SubunitAntibodies, NeutralizingAntibodies, ViralBroadly Neutralizing AntibodiesCOVID-19 VaccinesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Vaccines, SubunitViral VaccinesCOVID-19Microarray patchSARS-CoV-2Vaccine

Identifiers

PMID35871873
PMCPMC9291373
OpenAlexW4285736078

What OpenQuestion holds

Textmetadata
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.