Evidence map›Paper›PMID 33217916›Full record

ArticleVaccines2020

COVID-19 Infection Detection and Prevention by SARS-CoV-2 Active Antigens: A Synthetic Vaccine Approach.

José Manuel Lozano, Luz Mary Salazar, Ángela Torres, Adriana Arévalo-Jamaica, Carlos Franco-Muñoz, Marcela Mercado-Reyes, Fabio Ancizar Aristizabal

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2020. 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
0.1field-weighted citation impact, top 47% 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. Monkeypox: potential vaccine development strategies.Trends in pharmacological sciences · 2023
    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

7 authors at 2 institutions in 1 country.

José Manuel LozanoDepartamento de Farmacia, Universidad Nacional de Colombia- Sede Bogotá, Carrera 30#45-03, Bogotá DC 111321, Colombia.ORCID 0000-0001-6039-0213
Luz Mary SalazarGrupo de Investigación: Mimetismo Molecular de los Agentes Infecciosos, Departamento de Farmacia, Universidad Nacional de Colombia-Sede Bogotá, Carrera 30 #45-03, Bogotá DC 111321, Colombia.
Ángela TorresGrupo de Investigación: Mimetismo Molecular de los Agentes Infecciosos, Departamento de Farmacia, Universidad Nacional de Colombia-Sede Bogotá, Carrera 30 #45-03, Bogotá DC 111321, Colombia.
Adriana Arévalo-JamaicaDirección de Investigación en Salud Pública, Instituto Nacional de Salud, Bogotá 111321, Colombia.
Carlos Franco-MuñozDirección de Investigación en Salud Pública, Instituto Nacional de Salud, Bogotá 111321, Colombia.
Marcela Mercado-ReyesDirección de Investigación en Salud Pública, Instituto Nacional de Salud, Bogotá 111321, Colombia.
Fabio Ancizar AristizabalDepartamento de Farmacia, Universidad Nacional de Colombia- Sede Bogotá, Carrera 30#45-03, Bogotá DC 111321, Colombia.
Universidad Nacional de Colombia · COInstituto Nacional de Salud · CO

Funding

Universidad Nacional de Colombia HERMES-50090
6 · The paper itself

Abstract

COVID-19, a global pandemic causing to date more than 50 million cases and more than a million deaths, has to be controlled. SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) was identified as the causative agent. Controversy about this virus origin and infectious mechanism for adapting to humans remains a matter for discussion. Among all strategies for obtaining safe and potent vaccines, approaches based on attenuated-killed virus and non-replicating RNA viral vectors are demonstrating promising results. However, specificity of viral components targeted by human antibodies so far has not been demonstrated. A consistent strategy for obtaining functional-active antigens from SARS-CoV-2 specific ligands lead us to propose and test a number of synthetic components. From hundreds of starting sequences only fifteen fulfilled the design requirements and were produced as monomer and polymer forms and immuno-chemically tested. The design was based on worldwide representative reported virus genomes. A bioinformatics scheme by conventional methods and knowledge on MHC-I and II antigen processing mechanisms and HLA haplotype-restriction was performed including sensitive and resistant human populations to virus infection. Covid-19 patients' sera reactivity for synthetic SARS-CoV-2-designed components have proven a high recognition of specific molecules, as well as some evidence for a long-lasting humoral immune response.

Indexed as

antigen designCOVID-19SARS-CoV-2synthetic-vaccine candidate

Identifiers

PMID33217916
PMCPMC7712209
OpenAlexW3100639279

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.