Evidence map›Paper›PMID 35357709›Full record

ArticleAllergy2022

Vaccine based on folded receptor binding domain-PreS fusion protein with potential to induce sterilizing immunity to SARS-CoV-2 variants.

Pia Gattinger, Bernhard Kratzer, Inna Tulaeva, Katarzyna Niespodziana, Anna Ohradanova-Repic, Laura Gebetsberger, Kristina Borochova, Erika Garner-Spitzer, Doris Trapin, Gerhard Hofer and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Allergy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 28 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

19 authors at 7 institutions in 3 countries.

Pia GattingerDepartment of Pathophysiology and Allergy Research, Division of Immunopathology, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0001-6724-8543
Bernhard KratzerCenter for Pathophysiology, Infectiology and Immunology, Institute of Immunology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0003-1091-4327
Inna TulaevaDepartment of Pathophysiology and Allergy Research, Division of Immunopathology, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-5825-2687
Katarzyna NiespodzianaDepartment of Pathophysiology and Allergy Research, Division of Immunopathology, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0003-0700-965X
Anna Ohradanova-RepicCenter for Pathophysiology, Infectiology and Immunology, Institute for Hygiene and Applied Immunology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-8005-8522
Laura GebetsbergerCenter for Pathophysiology, Infectiology and Immunology, Institute for Hygiene and Applied Immunology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-6480-6228
Kristina BorochovaDepartment of Pathophysiology and Allergy Research, Division of Immunopathology, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Erika Garner-SpitzerInstitute of Specific Prophylaxis and Tropical Medicine, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-5283-0458
Doris TrapinCenter for Pathophysiology, Infectiology and Immunology, Institute of Immunology, Medical University of Vienna, Vienna, Austria.
Gerhard HoferDepartment of Materials and Environmental Chemistry, University of Stockholm, Stockholm, Sweden.
Walter KellerInstitute of Molecular Biosciences, BioTechMed Graz, University of Graz, Graz, Austria.ORCID 0000-0002-2261-958X
Isabella BaumgartnerDepartment of Ophthalmology, Medical University Vienna, Vienna, Austria.
Ivan TancevskiDepartment of Internal Medicine II, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0001-5116-8960
Musa KhaitovNRC Institute of Immunology FMBA of Russia, Moscow, Russia.ORCID 0000-0003-4961-9640
Alexander KaraulovLaboratory for Immunopathology, Department of Clinical Immunology and Allergology, Sechenov First Moscow State Medical University, Moscow, Russia.
Hannes StockingerCenter for Pathophysiology, Infectiology and Immunology, Institute for Hygiene and Applied Immunology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0001-6404-4430
Ursula WiedermannInstitute of Specific Prophylaxis and Tropical Medicine, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-1302-3223
Winfried F PicklCenter for Pathophysiology, Infectiology and Immunology, Institute of Immunology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0003-0430-4952
Rudolf ValentaDepartment of Pathophysiology and Allergy Research, Division of Immunopathology, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0001-5944-3365
Medical University of Vienna · ATSechenov University · RUKarl Landsteiner University of Health Sciences · ATInnsbruck Medical University · ATPirogov Russian National Research Medical University · RUStockholm University · SEUniversity of Graz · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is responsible for the ongoing global COVID-19 pandemic. One possibility to control the pandemic is to induce sterilizing immunity through the induction and maintenance of neutralizing antibodies preventing SARS-CoV-2 from entering human cells to replicate in.

methodsWe report the construction and in vitro and in vivo characterization of a SARS-CoV-2 subunit vaccine (PreS-RBD) based on a structurally folded recombinant fusion protein consisting of two SARS-CoV-2 Spike protein receptor-binding domains (RBD) fused to the N- and C-terminus of hepatitis B virus (HBV) surface antigen PreS to enable the two unrelated proteins serving as immunologic carriers for each other.

resultsPreS-RBD, but not RBD alone, induced a robust and uniform RBD-specific IgG response in rabbits. Currently available genetic SARS-CoV-2 vaccines induce mainly transient IgG

conclusionThe PreS-RBD vaccine has the potential to serve as a combination vaccine for inducing sterilizing immunity against SARS-CoV-2 and HBV by stopping viral replication through the inhibition of cellular virus entry.

Indexed as

COVID-19COVID-19 VaccinesSARS-CoV-2Spike Glycoprotein, CoronavirusAnimalsAntibodies, NeutralizingAntibodies, ViralHumansImmunoglobulin GPandemicsRabbitsAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesImmunoglobulin GSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2antibody responseCOVID-19neutralizing antibodiesSARS-CoV-2sterilizing immunityvaccine

Identifiers

PMID35357709
PMCPMC9111473
OpenAlexW4221108814

What OpenQuestion holds

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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.