Evidence map›Paper›PMID 34960155›Full record

ReviewVaccines2021

VLP-Based COVID-19 Vaccines: An Adaptable Technology against the Threat of New Variants.

Wasim A Prates-Syed, Lorena C S Chaves, Karin P Crema, Larissa Vuitika, Aline Lira, Nelson Côrtes, Victor Kersten, Francisco E G Guimarães, Mohammad Sadraeian, Fernando L Barroso da Silva and 5 more

Open access · goldAbstract readReview
In one paragraph

Review in Vaccines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.7field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Review
  3. Microbial Nanoparticles in Biological Plant Protection.International journal of molecular sciences · 2025
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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

15 authors at 4 institutions in 5 countries.

Wasim A Prates-SyedDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo (ICB/USP), São Paulo 05508000, SP, Brazil.ORCID 0000-0002-2032-3902
Lorena C S ChavesDepartment of Microbiology and Immunology, School of Medicine, Emory University, Claudia Nance Rollins Building, Atlanta, GA 30329, USA.ORCID 0000-0001-7515-0781
Karin P CremaDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo (ICB/USP), São Paulo 05508000, SP, Brazil.
Larissa VuitikaDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo (ICB/USP), São Paulo 05508000, SP, Brazil.
Aline LiraDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo (ICB/USP), São Paulo 05508000, SP, Brazil.ORCID 0000-0001-9405-4955
Nelson CôrtesDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo (ICB/USP), São Paulo 05508000, SP, Brazil.ORCID 0000-0002-6829-9075
Victor KerstenDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo (ICB/USP), São Paulo 05508000, SP, Brazil.
Francisco E G GuimarãesSão Carlos Institute of Physics, IFSC-USP, São Carlos 13566590, SP, Brazil.ORCID 0000-0002-2504-7812
Mohammad SadraeianSão Carlos Institute of Physics, IFSC-USP, São Carlos 13566590, SP, Brazil.ORCID 0000-0002-7384-2247
Fernando L Barroso da SilvaDepartment of Biomolecular Sciences, School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto 14040903, SP, Brazil.ORCID 0000-0003-2526-2085
Otávio Cabral-MarquesDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo (ICB/USP), São Paulo 05508000, SP, Brazil.ORCID 0000-0002-3183-6236
José A M BarbutoDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo (ICB/USP), São Paulo 05508000, SP, Brazil.ORCID 0000-0001-9526-6781
Momtchilo RussoDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo (ICB/USP), São Paulo 05508000, SP, Brazil.ORCID 0000-0003-3553-3184
Niels O S CâmaraDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo (ICB/USP), São Paulo 05508000, SP, Brazil.ORCID 0000-0001-5436-1248
Gustavo Cabral-MirandaDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo (ICB/USP), São Paulo 05508000, SP, Brazil.
Universidade de São Paulo · BREmory University · USNorth Carolina State University · USUniversity of Technology Sydney · AU

Funding

São Paulo Research Foundation 2019/14526-0 and 2020/05146-7
6 · The paper itself

Abstract

Virus-like particles (VLPs) are a versatile, safe, and highly immunogenic vaccine platform. Recently, there are developmental vaccines targeting SARS-CoV-2, the causative agent of COVID-19. The COVID-19 pandemic affected humanity worldwide, bringing out incomputable human and financial losses. The race for better, more efficacious vaccines is happening almost simultaneously as the virus increasingly produces variants of concern (VOCs). The VOCs Alpha, Beta, Gamma, and Delta share common mutations mainly in the spike receptor-binding domain (RBD), demonstrating convergent evolution, associated with increased transmissibility and immune evasion. Thus, the identification and understanding of these mutations is crucial for the production of new, optimized vaccines. The use of a very flexible vaccine platform in COVID-19 vaccine development is an important feature that cannot be ignored. Incorporating the spike protein and its variations into VLP vaccines is a desirable strategy as the morphology and size of VLPs allows for better presentation of several different antigens. Furthermore, VLPs elicit robust humoral and cellular immune responses, which are safe, and have been studied not only against SARS-CoV-2 but against other coronaviruses as well. Here, we describe the recent advances and improvements in vaccine development using VLP technology.

Indexed as

COVID-19SARS-CoV-2vaccinesvirus-like particles

Identifiers

PMID34960155
PMCPMC8708688
OpenAlexW3216059092

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.