Evidence map›Paper›PMID 32870446›Full record

ArticleMolecular biotechnology2020

An AMA1/MSP1

Evelia M Milán-Noris, Elizabeth Monreal-Escalante, Sergio Rosales-Mendoza, Ruth E Soria-Guerra, Osman Radwan, John A Juvik, Schuyler S Korban

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular biotechnology, 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
0.3field-weighted citation impact, top 41% 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, 7 citations in OpenAlex.

  1. Malaria: past, present, and future.Signal transduction and targeted therapy · 2025
    Review
  2. Review
  3. 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

7 authors at 3 institutions in 2 countries.

Evelia M Milán-NorisDivision of Nutritional Sciences, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA.
Elizabeth Monreal-EscalanteLaboratorio de Biofarmacéuticos Recombinantes, Facultad de Ciencias Químicas, Universidad Autónoma de San Luis Potosí, Av. Dr. Manuel Nava 6, 78210, San Luis Potosi, SLP, Mexico.
Sergio Rosales-MendozaLaboratorio de Biofarmacéuticos Recombinantes, Facultad de Ciencias Químicas, Universidad Autónoma de San Luis Potosí, Av. Dr. Manuel Nava 6, 78210, San Luis Potosi, SLP, Mexico. rosales.s@fcq.uaslp.mx.
Ruth E Soria-GuerraLaboratorio de Ingeniería de Biorreactores, Facultad de Ciencias Químicas, Universidad Autónoma de San Luis Potosí, Av. Dr. Manuel Nava 6, 78210, San Luis Potosi, SLP, Mexico.
Osman RadwanDepartment of Natural Resources and Environmental Sciences, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA.
John A JuvikDivision of Nutritional Sciences, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA.
Schuyler S KorbanDivision of Nutritional Sciences, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA. korban@illinois.edu.ORCID http://orcid.org/0000-0003-1544-5160
Autonomous University of San Luis Potosí · MXUniversity of Illinois Urbana-Champaign · USUniversity of Dayton · US

Funding

University of Illinois Office of Research Project no. 65-325
6 · The paper itself

Abstract

Malaria is a tropical human disease, caused by protozoan parasites, wherein a significant number of the world's population is at risk. Annually, more than 219 million new cases are reported. Although there are prevention treatments, there are no highly and widely effective licensed anti-malarial vaccines available for use. Opportunities for utilization of plant-based vaccines as novel platforms for developing safe, reliable, and affordable treatments offer promise for developing such a vaccine against malaria. In this study, a Malchloroplast candidate vaccine was designed, composed of segments of AMA1 and MSP1 proteins, two epitopes of Plasmodium falciparum, along with a GK1 peptide from Taenia solium as adjuvant, and this was expressed in tobacco chloroplasts. Transplastomic tobacco lines were generated using biolistic transformation, and these were confirmed to carry the synthetic gene construct. Expression of the synthetic GK1 peptide was confirmed using RT-PCR and Western blots. Furthermore, the GK1 peptide was detected by HPLC at levels of up to 6 µg g

Indexed as

ImmunityAdjuvants, ImmunologicAnimalsAntigens, ProtozoanFemaleGenetic VectorsHumansImmunoglobulin GMalaria, FalciparumMalaria VaccinesMice, Inbred BALB CNicotianaPeptidesPlants, Genetically ModifiedPlasmidsPlasmodium falciparumAdjuvants, ImmunologicAntigens, ProtozoanImmunoglobulin GMalaria VaccinesPeptidesHumoral responseMolecular farmingPlasmodium falciparumPlastid transformationPolycistronicTransplastomicsVaccine adjuvant

Identifiers

PMID32870446
OpenAlexW3082337202

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.