Evidence map›Paper›PMID 35631687›Full record

ArticlePharmaceutics2022

Development of an LNP-Encapsulated mRNA-RBD Vaccine against SARS-CoV-2 and Its Variants.

Cong Liu, Nino Rcheulishvili, Zhigao Shen, Dimitri Papukashvili, Fengfei Xie, Ziqian Wang, Xingyun Wang, Yunjiao He, Peng George Wang

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.4field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
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  5. Research Progress on Liposome Pulmonary Delivery ofJournal of aerosol medicine and pulmonary drug delivery · 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

9 authors at 1 institution in 1 country.

Cong LiuSchool of Medicine, Southern University of Science and Technology, Shenzhen 518000, China.
Nino RcheulishviliSchool of Medicine, Southern University of Science and Technology, Shenzhen 518000, China.ORCID 0000-0001-5982-8230
Zhigao ShenSchool of Medicine, Southern University of Science and Technology, Shenzhen 518000, China.
Dimitri PapukashviliSchool of Medicine, Southern University of Science and Technology, Shenzhen 518000, China.ORCID 0000-0002-4793-2636
Fengfei XieSchool of Medicine, Southern University of Science and Technology, Shenzhen 518000, China.
Ziqian WangSchool of Medicine, Southern University of Science and Technology, Shenzhen 518000, China.
Xingyun WangSchool of Medicine, Southern University of Science and Technology, Shenzhen 518000, China.
Yunjiao HeSchool of Medicine, Southern University of Science and Technology, Shenzhen 518000, China.
Peng George WangSchool of Medicine, Southern University of Science and Technology, Shenzhen 518000, China.ORCID 0000-0003-3335-6794
Southern University of Science and Technology · CN

Funding

COVID-19 Prevention and Control Special Project of Guangdong Education Department 2020KZDZX1181Shenzhen Overseas High Level Talent (Peacock Plan) Project KQTD20200909113758004
6 · The paper itself

Abstract

Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is undoubtedly the most challenging pandemic in the current century and remains a global health emergency. As the number of COVID-19 cases in the world is on the rise and variants continue to emerge, there is an urgent need for vaccines. Among all immunization approaches, mRNA vaccines have demonstrated more promising results in response to this challenge. Herein, we designed an mRNA-based vaccine encoding the receptor-binding domain (RBD) of SARS-CoV-2 encapsulated in lipid nanoparticles (LNPs). Intramuscular (i.m.) administration of the mRNA-RBD vaccine elicited broad-spectrum neutralizing antibodies and cellular responses against not only the wild-type SARS-CoV-2 virus but also Delta and Omicron variants. These results indicated that two doses of mRNA-RBD immunization conferred a strong immune response in mice against the wild-type SARS-CoV-2, while the booster dose provided a sufficient immunity against SARS-CoV-2 and its variants. Taken together, the three-dose regimen strategy of the mRNA-RBD vaccine proposed in the present study appears to be a promising reference for the development of mRNA vaccines targeting SARS-CoV-2 variants.

Indexed as

COVID-19DeltaLNPsmRNA vaccineneutralizing antibodiesOmicronRBDSARS-CoV-2

Identifiers

PMID35631687
PMCPMC9143166
OpenAlexW4281252060

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.