Evidence map›Paper›PMID 38753442›Full record

ArticleEuropean journal of microbiology & immunology2024

Preclinical assessment of a recombinant RBD-Fc fusion protein as SARS-CoV-2 candidate vaccine.

Navid Dashti, Forough Golsaz-Shirazi, Haleh Soltanghoraee, Amir-Hassan Zarnani, Mehdi Mohammadi, Danyal Imani, Mahmood Jeddi-Tehrani, Mohammad Mehdi Amiri, Fazel Shokri

Abstract read
In one paragraph

Article in European journal of microbiology & immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

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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

9 authors.

Navid Dashti1Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Forough Golsaz-Shirazi1Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Haleh Soltanghoraee2Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Amir-Hassan Zarnani1Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Mehdi Mohammadi4Department of Medical Immunology, School of Medicine, Tehran University of Medical Sciences (TUMS), Tehran, Iran.
Danyal Imani1Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Mahmood Jeddi-Tehrani5Monoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Mohammad Mehdi Amiri1Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Fazel Shokri1Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.ORCID 0000-0003-2940-3404

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Waning immunity and emergence of new variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), highlight the need for further research in vaccine development. Methods: A recombinant fusion protein containing the receptor-binding domain (RBD) fused to the human IgG1 Fc (RBD-Fc) was produced in CHO-K1 cells. RBD-Fc was emulsified with four adjuvants to evaluate its immunogenicity. The RBD-specific humoral and cellular immune responses were assessed by ELISA. The virus neutralizing potency of the vaccine was investigated using four neutralization methods. Safety was studied in mice and rabbits, and Antibody-Dependent Enhancement (ADE) effects were investigated by flow cytometry. Results: RBD-Fc emulsified in Alum induced a high titer of anti-RBD antibodies with remarkable efficacy in neutralizing both pseudotyped and live SARS-CoV-2 Delta variant. The neutralization potency dropped significantly in response to the Omicron variant. RBD-Fc induced both TH2 and particularly TH1 immune responses. Histopathologic examinations demonstrated no substantial pathologic changes in different organs. No changes in serum biochemical and hematologic parameters were observed. ADE effect was not observed following immunization with RBD-Fc. Conclusion: RBD-Fc elicits highly robust neutralizing antibodies and cellular immune responses, with no adverse effects. Therefore, it could be considered a promising and safe subunit vaccine against SARS-CoV-2.

Indexed as

immunogenicityneutralizationRBD-FcsafetySARS-CoV-2vaccine

Identifiers

PMID38753442
PMCPMC11393645

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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.