Evidence map›Paper›PMID 35527696›Full record

ArticleJournal of clinical laboratory analysis2022

Nucleocapsid protein of SARS-CoV-2 is a potential target for developing new generation of vaccine.

Weixu Feng, Yunru Xiang, Lianpeng Wu, Zhuo Chen, Qingfeng Li, Jun Chen, Yanru Guo, Dandan Xia, Na Chen, Lifang Zhang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
5.6field-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

31 citing papers in PubMed, 56 citations in OpenAlex.

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  12. Molecular characterization of SARS-CoV-2 nucleocapsid protein.Frontiers in cellular and infection microbiology · 2024
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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

12 authors at 3 institutions in 2 countries.

Weixu FengSchool of Basic Medical Science, Wenzhou Medical University, Wenzhou, China.
Yunru XiangSchool of Basic Medical Science, Wenzhou Medical University, Wenzhou, China.
Lianpeng WuDepartment of Laboratory Medicine, The Sixth People Hospital of Wenzhou, Wenzhou, China.
Zhuo ChenSchool of Basic Medical Science, Wenzhou Medical University, Wenzhou, China.
Qingfeng LiSchool of Basic Medical Science, Wenzhou Medical University, Wenzhou, China.
Jun ChenSchool of Basic Medical Science, Wenzhou Medical University, Wenzhou, China.
Yanru GuoSchool of Basic Medical Science, Wenzhou Medical University, Wenzhou, China.
Dandan XiaDepartment of Laboratory Medicine, The Sixth People Hospital of Wenzhou, Wenzhou, China.
Na ChenDepartment of Laboratory Medicine, The Sixth People Hospital of Wenzhou, Wenzhou, China.
Lifang ZhangSchool of Basic Medical Science, Wenzhou Medical University, Wenzhou, China.
Shanli ZhuSchool of Basic Medical Science, Wenzhou Medical University, Wenzhou, China.ORCID https://orcid.org/0000-0002-6539-8078
Kong-Nan ZhaoSchool of Basic Medical Science, Wenzhou Medical University, Wenzhou, China.
Wenzhou Medical University · CNWenzhou City People's Hospital · CNThe University of Queensland · AU

Funding

Key Projects of Health and Hygiene WKJ-ZJ-2138
6 · The paper itself

Abstract

backgroundSARS-CoV-2 has spread worldwide causing more than 400 million people with virus infections since early 2020. Currently, the existing vaccines targeting the spike glycoprotein (S protein) of SARS-CoV-2 are facing great challenge from the infection of SARS-CoV-2 virus and its multiple S protein variants. Thus, we need to develop a new generation of vaccines to prevent infection of the SARS-CoV-2 variants. Compared with the S protein, the nucleocapsid protein (N protein) of SARS-CoV-2 is more conservative and less mutations, which also plays a vital role in viral infection. Therefore, the N protein may have the great potential for developing new vaccines.

methodsThe N protein of SARS-CoV-2 was recombinantly expressed and purified in Escherichia coli. Western Blot and ELISA assays were used to demonstrate the immunoreactivity of the recombinant N protein with the serum of 22 COVID-19 patients. We investigated further the response of the specific serum antibodies and cytokine production in BALB/c mice immunized with recombinant N protein by Western Blot and ELISA.

resultsThe N protein had good immunoreactivity and the production of IgG antibody against N protein in COVID-19 patients was tightly correlated with disease severity. Furthermore, the N protein was used to immunize BALB/c mice to have elicited strong immune responses. Not only high levels of IgG antibody, but also cytokine-IFN-γ were produced in the N protein-immunized mice. Importantly, the N protein immunization induced a high level of IgM antibody produced in the mice.

conclusionSARS-CoV-2 N protein shows a great big bundle of potentiality for developing a new generation of vaccines in fighting infection of SARS-CoV-2 and its variants.

Indexed as

COVID-19VaccinesAnimalsAntibodies, ViralCytokinesHumansImmunoglobulin GMiceMice, Inbred BALB CNucleocapsid ProteinsSARS-CoV-2Spike Glycoprotein, CoronavirusAntibodies, ViralCytokinesImmunoglobulin GNucleocapsid ProteinsSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Vaccinesantibodyimmune responsenucleocapsid proteinSARS-CoV-2vaccine

Identifiers

PMID35527696
PMCPMC9169192
OpenAlexW4229372745

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.