Evidence map›Paper›PMID 37863669›Full record

ArticleVaccine2023

Advax-CpG55.2-adjuvanted monovalent or trivalent SARS-CoV-2 recombinant spike protein vaccine protects hamsters against heterologous infection with Beta or Delta variants.

Yoshikazu Honda-Okubo, Richard Bowen, Mckinzee Barker, Helle Bielefeldt-Ohmann, Nikolai Petrovsky

Open access · greenAbstract read
In one paragraph

Article in Vaccine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Trial
  2. Trial
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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

5 authors at 4 institutions in 2 countries.

Yoshikazu Honda-OkuboVaxine Pty Ltd., Bedford Park, Adelaide, SA 5042, Australia; College of Medicine and Public Health, Flinders University, Adelaide, SA 5042, Australia.
Richard BowenDepartment of Biomedical Sciences, Colorado State University, Fort Collins, CO 80523, USA.
Mckinzee BarkerDepartment of Biomedical Sciences, Colorado State University, Fort Collins, CO 80523, USA.
Helle Bielefeldt-OhmannSchool of Chemistry & Molecular Biosciences, The University of Queensland, St. Lucia, Qld 4072, Australia.
Nikolai PetrovskyVaxine Pty Ltd., Bedford Park, Adelaide, SA 5042, Australia. Electronic address: nikolai.petrovsky@vaxine.net.
Colorado State University · USFlinders University · AUThe University of Queensland · AUVaxine (Australia) · AU

Funding

NIAID NIH HHS HHSN272200800039CNIAID NIH HHS HHSN272201400053CNIAID NIH HHS HHSN272201800024CNIAID NIH HHS HHSN272201800044C
6 · The paper itself

Abstract

The ongoing evolution of SARS-CoV-2 variants emphasizes the need for vaccines providing broad cross-protective immunity. This study was undertaken to assess the ability of Advax-CpG55.2 adjuvanted monovalent recombinant spike protein (Wuhan, Beta, Gamma) vaccines or a trivalent formulation to protect hamsters againstBeta or Delta virus infection. The ability of vaccines to block virus transmission to naïve co-housed animals was also assessed. In naïve hosts, the Beta variant induced higher virus loads than the Delta variant, and conversely the Delta variant caused more severe disease and was more likely to be associated with virus transmission. The trivalent vaccine formulation provided the best protection against both Beta and Delta infection and also completely prevented virus transmission. The next best performing vaccine was the original monovalent Wuhan-based vaccine. Notably, hamsters that received the monovalent Gamma spike vaccine had the highest viral loads and clinical disease of all the vaccine groups, a potential signal of antibody dependent-enhancement (ADE). These hamsters were also the most likely to transmit Delta virus to naïve recipients. In murine studies, the Gamma spike vaccine induced the highest total spike protein to RBD IgG ratio and the lowest levels of neutralizing antibody, a context that could predispose to ADE. Overall, the study results confirmed that the current SpikoGen® vaccine based on Wuhan spike protein was still able to protect against clinical disease caused by either the Beta or Delta virus variants but suggested additional protection may be obtained by combining it with extra variant spike proteins to make a multivalent formulation. This study highlights the complexity of optimizing vaccine protection against multiple SARS-CoV-2 variants and stresses the need to continue to pursue new and improved COVID-19 vaccines able to provide robust, long-lasting, and broadly cross-protective immunity against constantly evolving SARS-CoV-2 variants.

Indexed as

COVID-19VaccinesAdjuvants, ImmunologicAnimalsAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesCricetinaeHumansInulinMiceSARS-CoV-2Spike Glycoprotein, CoronavirusAdjuvants, ImmunologicAntibodies, NeutralizingAntibodies, ViralCOVID-19 Vaccinesdelta inulinInulinSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2VaccinesAdjuvantAdvaxCoronavirusCOVID-19PandemicSARS-Cov-2Vaccine

Identifiers

PMID37863669
PMCPMC10873063
OpenAlexW4387749417

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.