Evidence map›Paper›PMID 35603198›Full record

ArticleFrontiers in immunology2022

Design of a Recombinant Multivalent Epitope Vaccine Based on SARS-CoV-2 and Its Variants in Immunoinformatics Approaches.

Mingkai Yu, Yuejie Zhu, Yujiao Li, Zhiqiang Chen, Zhiwei Li, Jing Wang, Zheng Li, Fengbo Zhang, Jianbing Ding

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

29 citing papers in PubMed, 39 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

9 authors at 2 institutions in 1 country.

Mingkai YuDepartment of Immunology, School of Basic Medical Sciences, Xinjiang Medical University, Urumqi, China.
Yuejie ZhuReproductive Medicine Center, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Yujiao LiDepartment of Blood Transfusion, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Zhiqiang ChenDepartment of Immunology, School of Basic Medical Sciences, Xinjiang Medical University, Urumqi, China.
Zhiwei LiClinical Laboratory Center, Xinjiang Uygur Autonomous Region People's Hospital, Urumqi, China.
Jing WangXinjiang Laboratory of Respiratory Disease Research, Traditional Chinese Medicine Hospital Affiliated to Xinjiang Medical University, Urumqi, China.
Zheng LiXinjiang Laboratory of Respiratory Disease Research, Traditional Chinese Medicine Hospital Affiliated to Xinjiang Medical University, Urumqi, China.
Fengbo ZhangDepartment of Clinical Laboratory, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Jianbing DingDepartment of Immunology, School of Basic Medical Sciences, Xinjiang Medical University, Urumqi, China.
Xinjiang Medical University · CNFirst Affiliated Hospital of Xinjiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of an effective multivalent vaccine against SARS-CoV-2 variants is an important means to improve the global public health situation caused by COVID-19. In this study, we identified the antigen epitopes of the main global epidemic SARS-CoV-2 and mutated virus strains using immunoinformatics approach, and screened out 8 cytotoxic T lymphocyte epitopes (CTLEs), 17 helper T lymphocyte epitopes (HTLEs), 9 linear B-cell epitopes (LBEs) and 4 conformational B-cell epitopes (CBEs). The global population coverage of CTLEs and HTLEs was 93.16% and 99.9% respectively. These epitopes were spliced together by corresponding linkers and recombined into multivalent vaccine. In silico tests, the vaccine protein was a non-allergen and the docking with TLR-3 molecule showed a strong interaction. The results of immune simulation showed that the vaccine may be helpful to initiate both cellular and humoral immunity against all VOC. The optimistic immunogenicity of the vaccine was confirmed

Indexed as

COVID-19SARS-CoV-2COVID-19 VaccinesEpitopes, B-LymphocyteEpitopes, T-LymphocyteHumansMolecular Docking SimulationVaccines, CombinedCOVID-19 VaccinesEpitopes, B-LymphocyteEpitopes, T-LymphocyteVaccines, CombinedCOVID-19epitopeimmunoinformaticsSARS-CoV-2vaccinevariant

Identifiers

PMID35603198
PMCPMC9120605
OpenAlexW4229065141

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.