Evidence map›Paper›PMID 37751460›Full record

ArticlePloS one2023

Production and characterization of a chimeric antigen, based on nucleocapsid of SARS-CoV-2 fused to the extracellular domain of human CD154 in HEK-293 cells as a vaccine candidate against COVID-19.

Thailin Lao, Ileanet Avalos, Elsa María Rodríguez, Yasser Zamora, Alianet Rodriguez, Ailyn Ramón, Yanitza Alvarez, Ania Cabrales, Ivan Andújar, Luis Javier González and 6 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

16 authors at 1 institution in 1 country.

Thailin LaoCenter for Genetic Engineering and Biotechnology, Animal Biotechnology Department, Havana, Cuba.
Ileanet AvalosCenter for Genetic Engineering and Biotechnology, Animal Biotechnology Department, Havana, Cuba.
Elsa María RodríguezCenter for Genetic Engineering and Biotechnology, Animal Biotechnology Department, Havana, Cuba.
Yasser ZamoraCenter for Genetic Engineering and Biotechnology, Animal Biotechnology Department, Havana, Cuba.
Alianet RodriguezCenter for Genetic Engineering and Biotechnology, Animal Biotechnology Department, Havana, Cuba.
Ailyn RamónCenter for Genetic Engineering and Biotechnology, Laboratory of Molecular Oncology, Havana, Cuba.
Yanitza AlvarezCenter for Genetic Engineering and Biotechnology, Animal Biotechnology Department, Havana, Cuba.
Ania CabralesCenter for Genetic Engineering and Biotechnology, Systems Biology, Havana, Cuba.
Ivan AndújarCenter for Genetic Engineering and Biotechnology, Systems Biology, Havana, Cuba.
Luis Javier GonzálezCenter for Genetic Engineering and Biotechnology, Systems Biology, Havana, Cuba.
Pedro PuenteCenter for Genetic Engineering and Biotechnology, Animal housing, Havana, Cuba.
Cristina GarcíaCenter for Genetic Engineering and Biotechnology, Production Division, Havana, Cuba.
Leonardo GómezCenter for Genetic Engineering and Biotechnology, Production Division, Havana, Cuba.
Rodolfo ValdésCenter for Genetic Engineering and Biotechnology, Production Division, Havana, Cuba.
Mario Pablo EstradaCenter for Genetic Engineering and Biotechnology, Animal Biotechnology Department, Havana, Cuba.
Yamila CarpioCenter for Genetic Engineering and Biotechnology, Animal Biotechnology Department, Havana, Cuba.
Centro de Ingeniería Genética y Biotecnología · CU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite that more than one hundred vaccines against SARS-CoV-2 have been developed and that some of them were evaluated in clinical trials, the latest results revealed that these vaccines still face great challenges. Among the components of the virus, the N-protein constitutes an attractive target for a subunit vaccine because it is the most abundant, highly conserved and immunogenic protein. In the present work, a chimeric protein (N-CD protein) was constructed by the fusion of the N-protein to the extracellular domain of human CD154 as the molecular adjuvant. HEK-293 cells were transduced with lentiviral vector bearing the N-CD gene and polyclonal cell populations were obtained. The N-CD protein was purified from cell culture supernatant and further characterized by several techniques. Immunogenicity studies in mice and non-human primates showed the N-CD protein induced high IgG titers in both models after two doses. Moreover, overall health monitoring of non-human primates demonstrated that animals were healthy during 228 days after first immunization. Data obtained support further investigation in order to develop this chimeric protein as vaccine candidate against COVID-19 and other coronavirus diseases.

Indexed as

COVID-19VaccinesAnimalsCD40 LigandCOVID-19 VaccinesHEK293 CellsHumansMiceNucleocapsidRecombinant Fusion ProteinsSARS-CoV-2CD40 LigandCOVID-19 VaccinesRecombinant Fusion ProteinsVaccines

Identifiers

PMID37751460
PMCPMC10522030
OpenAlexW4387043455

What OpenQuestion holds

Textmetadata
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.