Evidence map›Paper›PMID 41667669›Full record

ArticleScientific reports2026

Expanding SARS-CoV-2 antigen targets beyond spike using a baculovirus expression system.

Adnan Asadbeigi, Amirhossein Razavirad, Fatemeh Khajehahmadi, Mohsen Eghtedari, Reza Shirkoohi

Abstract readDataset
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Adnan AsadbeigiCancer Biology Research Center, Cancer Institute of Iran, Tehran University of Medical Sciences, Tehran, Iran.
Amirhossein RazaviradCancer Biology Research Center, Cancer Institute of Iran, Tehran University of Medical Sciences, Tehran, Iran.
Fatemeh KhajehahmadiDepartment of Medical Genetics, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Mohsen EghtedariCancer Biology Research Center, Cancer Institute of Iran, Tehran University of Medical Sciences, Tehran, Iran.
Reza ShirkoohiCancer Biology Research Center, Cancer Institute of Iran, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran. rshirkoohi@tums.ac.ir.

Funding

Tehran University of Medical Sciences and Health Services 99-1-228-47605
6 · The paper itself

Abstract

The ongoing antigenic evolution of SARS-CoV-2, particularly within the spike glycoprotein, threatens the long-term efficacy of spike-focused vaccines and serodiagnostics. While most authorized COVID-19 vaccines exclusively target the spike protein, growing evidence underscores multivalent strategies incorporating conserved viral antigens. Here, we employed a baculovirus expression vector system (BEVS) to co-express all four structural proteins, including spike, nucleocapsid, membrane, and envelope, in Sf9 insect cells. Surface-displayed antigens were used in a cell-based ELISA to profile IgG responses in convalescent sera. All antigens elicited detectable antibody binding, with nucleocapsid and membrane proteins provoking significantly stronger responses than spike (p < 0.001), and envelope protein showing intermediate reactivity. Statistical analyses revealed distinct patterns of antigenic reactivity. These findings validate the utility of BEVS for multiplex antigen presentation and highlight the immunological and diagnostic value of conserved non-spike antigens. Combined, this study advocates multivalent vaccine strategies and refines serodiagnostics by leveraging broader antigenic targets to counter immune escape.

Indexed as

Antibodies, ViralBaculoviridaeSARS-CoV-2Spike Glycoprotein, CoronavirusCOVID-19COVID-19 Serological TestingCOVID-19 VaccinesDNA, RecombinantGenetic VectorsHumansImmunoglobulin GSf9 CellsAntibodies, ViralCOVID-19 VaccinesDNA, RecombinantImmunoglobulin GSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Baculovirus expression vector systemIn-cell ELISA platformNext-generation vaccine platformSARS-CoV-2 structural antigens

Identifiers

PMID41667669
PMCPMC12963416

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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.