Evidence map›Paper›PMID 31959159›Full record

ArticleBMC biotechnology2020

A self-aggregating peptide: implications for the development of thermostable vaccine candidates.

Adolfo Cruz-Reséndiz, Jesús Zepeda-Cervantes, Alicia Sampieri, Carlos Bastián-Eugenio, Gonzalo Acero, J Iván Sánchez-Betancourt, Goar Gevorkian, Luis Vaca

Open access · goldAbstract read
In one paragraph

Article in BMC biotechnology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Development of thermostable vaccine adjuvants.Expert review of vaccines · 2021
    Review
  4. Article
  5. Review
  6. Article
  7. Review
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

8 authors at 2 institutions in 2 countries.

Adolfo Cruz-ReséndizInstituto de Fisiología Celular, Universidad Nacional Autónoma de México, CDMX 04510, Mexico City, Mexico.
Jesús Zepeda-CervantesInstituto de Fisiología Celular, Universidad Nacional Autónoma de México, CDMX 04510, Mexico City, Mexico.
Alicia SampieriInstituto de Fisiología Celular, Universidad Nacional Autónoma de México, CDMX 04510, Mexico City, Mexico.
Carlos Bastián-EugenioInstituto de Fisiología Celular, Universidad Nacional Autónoma de México, CDMX 04510, Mexico City, Mexico.
Gonzalo AceroInstituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, CDMX 04510, Mexico City, Mexico.
J Iván Sánchez-BetancourtFacultad de Medicina Veterinaria y Zootecnia, Universidad Nacional Autónoma de México, CDMX 04510, Mexico City, Mexico.
Goar GevorkianInstituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, CDMX 04510, Mexico City, Mexico.
Luis VacaInstituto de Fisiología Celular, Universidad Nacional Autónoma de México, CDMX 04510, Mexico City, Mexico. lvaca@ifc.unam.mx.ORCID 0000-0003-2266-4847
Universidad Nacional Autónoma de México · MXUniversity of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe use of biomaterials has been expanded to improve the characteristics of vaccines. Recently we have identified that the peptide PH

resultsIn the present study we demonstrate the use of a system developed to generate nano and microparticles carrying as a fusion protein peptides or proteins of interest to be used as vaccines. These particles are purified easily by centrifugation. Immunization of animals with the particles in the absence of adjuvant result in a robust and long-lasting immune response. Proteins contained inside the particles are maintained for over 1 year at ambient temperature, preserving their immunological properties.

conclusionThe rapid and efficient production of the particles in addition to the robust immune response they generate position this system as an excellent method for the rapid response against emerging diseases. The thermostability conferred by the particle system facilitates the distribution of the vaccines in developing countries or areas with no electricity.

Indexed as

AnimalsAntigensDrug StabilityFemaleGreen Fluorescent ProteinsImmunizationImmunoglobulinsMiceNanoparticlesOcclusion Body Matrix ProteinsParticle SizePeptidesProtein AggregatesRecombinant Fusion ProteinsThermodynamicsVaccinesAntigensGreen Fluorescent ProteinsImmunoglobulinsOcclusion Body Matrix ProteinsPeptidesProtein AggregatesRecombinant Fusion ProteinsVaccinesImmunologyParticlesSelf-assemblingThermostableVaccines

Identifiers

PMID31959159
PMCPMC6971912
OpenAlexW3006209267

What OpenQuestion holds

Textmetadata
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.