Evidence map›Paper›PMID 37199229›Full record

Trial reportImmunology2023

Ability of SpikoGen®, an Advax-CpG adjuvanted recombinant spike protein vaccine, to induce cross-neutralising antibodies against SARS-CoV-2 variants.

Yoshikazu Honda-Okubo, Anna Antipov, Greiciely Andre, Saghar Barati, Hamidreza Kafi, Nikolai Petrovsky

Open access · bronzeAbstract readRandomized Controlled TrialClinical Trial, Phase II
In one paragraph

Trial report in Immunology, 2023. 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
2.3field-weighted citation impact, top 12% 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, 12 citations in OpenAlex.

  1. Trial
  2. Molecular mechanisms of SARS-CoV-2 entry: implications for biomedical strategies.Microbiology and molecular biology reviews : MMBR · 2025
    Review
  3. Broadly active intranasal influenza vaccine with a nanocomplex particulate adjuvant targeting mast cells and toll-like receptor 9.Journal of controlled release : official journal of the Controlled Release Society · 2025
    Article
  4. Article
  5. Design and Synthesis of Polyphenolic Imidazo[4,5-ACS pharmacology & translational science · 2024
    Article
  6. Article
  7. Review
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

6 authors at 2 institutions in 1 country.

Yoshikazu Honda-OkuboVaxine Pty Ltd, Adelaide, South Australia, Australia.ORCID 0000-0002-2872-8621
Anna AntipovVaxine Pty Ltd, Adelaide, South Australia, Australia.ORCID 0000-0001-6557-7781
Greiciely AndreVaxine Pty Ltd, Adelaide, South Australia, Australia.ORCID 0000-0002-2467-4291
Saghar BaratiMedical Department, Orchid Pharmed Company, Tehran, Iran.ORCID 0000-0002-5620-338X
Hamidreza KafiMedical Department, Orchid Pharmed Company, Tehran, Iran.
Nikolai PetrovskyVaxine Pty Ltd, Adelaide, South Australia, Australia.ORCID 0000-0002-1580-5245
Vaxine (Australia) · AUFlinders University · AU

Funding

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

Abstract

SpikoGen® vaccine is a subunit COVID-19 vaccine expressed in insect cells comprising recombinant spike protein extracellular domain formulated with Advax-CpG55.2™ adjuvant. A Phase 2 trial was conducted in 400 adult participants randomised 3:1 to receive two intramuscular doses of SpikoGen® vaccine or saline placebo 3 weeks apart. Some Phase 2 trial participants later enrolled in a separate booster study and received a third dose of SpikoGen® vaccine. This stored serum was used to assess the ability of SpikoGen® vaccine to induce cross-neutralising antibodies against SARS-CoV-2 variants of concern. Sera taken at baseline and 2 weeks after the second vaccine dose from baseline seronegative Phase 2 subjects was evaluated using a panel of spike pseudotype lentivirus neutralisation assays for the ability to cross-neutralise a wide range of SARS-CoV-2 variants, including Omicron BA.1, BA.2 and BA.4/5. Stored samples of subjects who participated in both the 2-dose Phase 2 trial and a third dose booster trial 6 months later were also analysed for changes in cross-neutralising antibodies over time and dose. Two weeks after the second dose, sera broadly cross-neutralised most variants of concern, albeit with titres against Omicron variants being ~10-fold lower. While Omicron titres fell to low levels 6 months after the second vaccine dose in most subjects, they showed a ~20-fold rise after the third dose booster, after which there was only a ~2-3-fold difference in neutralisation of Omicron and the ancestral strains. Despite being based on the ancestral Wuhan sequence, after two doses, SpikoGen® vaccine induced broadly cross-neutralising serum antibodies. Titres then reduced over time but were rapidly restored by a third dose booster. This resulted in high neutralisation including against the Omicron variants. This data supports ongoing use of SpikoGen® vaccine for protection against recent SARS-CoV-2 Omicron variants.

Indexed as

COVID-19COVID-19 VaccinesAdjuvants, ImmunologicAdultAntibodies, NeutralizingAntibodies, ViralBroadly Neutralizing AntibodiesHumansInulinSARS-CoV-2Spike Glycoprotein, CoronavirusVaccines, SubunitVaccines, SyntheticAdjuvants, ImmunologicAntibodies, NeutralizingAntibodies, ViralBroadly Neutralizing AntibodiesCOVID-19 Vaccinesdelta inulinInulinSARS-CoV-2 recombinant spike protein with delta inulin and CpG-ODN adjuvant vaccineSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Vaccines, SubunitVaccines, Syntheticantibodiesimmunotherapylungvaccination

Identifiers

PMID37199229
PMCPMC10524547
OpenAlexW4377011856

What OpenQuestion 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 OpenQuestion graph.