Evidence map›Paper›PMID 36845030›Full record

ArticleiScience2023

Incorporation of SARS-CoV-2 spike NTD to RBD protein vaccine improves immunity against viral variants.

Isabelle Montgomerie, Thomas W Bird, Olga R Palmer, Ngarangi C Mason, Theresa E Pankhurst, Blair Lawley, Leonor C Hernández, Rhodri Harfoot, Astrid Authier-Hall, Danielle E Anderson and 16 more

Open access · goldAbstract read
In one paragraph

Article in iScience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
5.2field-weighted citation impact, top 3% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Synthetic host defense peptide inhibits SARS-CoV-2 replicationAntimicrobial agents and chemotherapy · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Advancements in the Development of Anti-SARS-CoV-2 Therapeutics.International journal of molecular sciences · 2024
    Review
  11. Article
  12. Article
  13. Article
  14. 1-L Transcription of SARS-CoV-2 Spike Protein S1 Subunit.International journal of molecular sciences · 2024
    Article
  15. Article
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

26 authors at 5 institutions in 3 countries.

Isabelle MontgomerieSchool of Biological Sciences, Victoria University of Wellington, Wellington, New Zealand.
Thomas W BirdSchool of Biological Sciences, Victoria University of Wellington, Wellington, New Zealand.
Olga R PalmerMalaghan Institute of Medical Research, Wellington, New Zealand.
Ngarangi C MasonMalaghan Institute of Medical Research, Wellington, New Zealand.
Theresa E PankhurstMalaghan Institute of Medical Research, Wellington, New Zealand.
Blair LawleyDepartment of Microbiology and Immunology, School of Biomedical Sciences, University of Otago, Dunedin, New Zealand.
Leonor C HernándezDepartment of Microbiology and Immunology, School of Biomedical Sciences, University of Otago, Dunedin, New Zealand.
Rhodri HarfootDepartment of Microbiology and Immunology, School of Biomedical Sciences, University of Otago, Dunedin, New Zealand.
Astrid Authier-HallMalaghan Institute of Medical Research, Wellington, New Zealand.
Danielle E AndersonDepartment of Microbiology and Immunology, University of Melbourne, at The Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia.
Kerry L HilliganMalaghan Institute of Medical Research, Wellington, New Zealand.
Kaitlin H BuickMalaghan Institute of Medical Research, Wellington, New Zealand.
Naasson M MbenzaSchool of Biological Sciences, Victoria University of Wellington, Wellington, New Zealand.
Gerd MittelstädtFerrier Research Institute, Victoria University of Wellington, Wellington, New Zealand.
Samara MaxwellSchool of Biological Sciences, Victoria University of Wellington, Wellington, New Zealand.
Shubhra SinhaDepartment of Microbiology and Immunology, School of Biomedical Sciences, University of Otago, Dunedin, New Zealand.
Joanna KuangDepartment of Microbiology and Immunology, School of Biomedical Sciences, University of Otago, Dunedin, New Zealand.
Kanta SubbaraoDepartment of Microbiology and Immunology, University of Melbourne, at The Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia.
Emily J ParkerFerrier Research Institute, Victoria University of Wellington, Wellington, New Zealand.
Alan SherLaboratory of Parasitic Diseases, National Institutes of Health, Bethesda, MD, USA.
Ian F HermansMalaghan Institute of Medical Research, Wellington, New Zealand.
James E UssherDepartment of Microbiology and Immunology, School of Biomedical Sciences, University of Otago, Dunedin, New Zealand.
Miguel E Quiñones-MateuDepartment of Microbiology and Immunology, School of Biomedical Sciences, University of Otago, Dunedin, New Zealand.
Davide ComolettiSchool of Biological Sciences, Victoria University of Wellington, Wellington, New Zealand.
Lisa M ConnorSchool of Biological Sciences, Victoria University of Wellington, Wellington, New Zealand.
VAANZ Group
Malaghan Institute of Medical Research · NZUniversity of Otago · NZVictoria University of Wellington · NZNational Institutes of Health · USThe University of Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging SARS-CoV-2 variants pose a threat to human health worldwide. SARS-CoV-2 receptor binding domain (RBD)-based vaccines are suitable candidates for booster vaccines, eliciting a focused antibody response enriched for virus neutralizing activity. Although RBD proteins are manufactured easily, and have excellent stability and safety properties, they are poorly immunogenic compared to the full-length spike protein. We have overcome this limitation by engineering a subunit vaccine composed of an RBD tandem dimer fused to the N-terminal domain (NTD) of the spike protein. We found that inclusion of the NTD (1) improved the magnitude and breadth of the T cell and anti-RBD response, and (2) enhanced T follicular helper cell and memory B cell generation, antibody potency, and cross-reactive neutralization activity against multiple SARS-CoV-2 variants, including B.1.1.529 (Omicron BA.1). In summary, our uniquely engineered RBD-NTD-subunit protein vaccine provides a promising booster vaccination strategy capable of protecting against known SARS-CoV-2 variants of concern.

Indexed as

ImmunologyVirology

Identifiers

PMID36845030
PMCPMC9940465
OpenAlexW4321368122

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.