Evidence map›Paper›PMID 31882925›Full record

ArticleScientific reports2019

Oral treatment with T6-loaded yeast cell wall particles reduces the parasitemia in murine visceral leishmaniasis model.

Débora B Scariot, Hélito Volpato, Nilma S Fernandes, Danielle Lazarin-Bidóia, Olga Borges, Maria do Céu Sousa, Fernanda A Rosa, Andrey P Jacomini, Sueli O Silva, Tânia Ueda-Nakamura and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 25% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Cell Death and Unprecedent Cytoskeletal Changes inChemical & biomedical imaging · 2026
    Article
  2. NRF2 signaling drives chemoresistance in NSCLC and glioblastoma.Molecular and cellular biochemistry · 2026
    Article
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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

12 authors at 2 institutions in 2 countries.

Débora B ScariotLaboratório de Inovação Tecnológica no Desenvolvimento de Fármacos e Cosméticos, State University of Maringá, Maringa, 87020-900, Brazil.
Hélito VolpatoLaboratório de Inovação Tecnológica no Desenvolvimento de Fármacos e Cosméticos, State University of Maringá, Maringa, 87020-900, Brazil.
Nilma S FernandesCellular Biology Graduate Program, State University of Maringá, Maringa, 87020-900, Brazil.ORCID http://orcid.org/0000-0002-2824-0618
Danielle Lazarin-BidóiaLaboratório de Inovação Tecnológica no Desenvolvimento de Fármacos e Cosméticos, State University of Maringá, Maringa, 87020-900, Brazil.ORCID http://orcid.org/0000-0003-2579-0048
Olga BorgesFaculty of Pharmacy, University of Coimbra, Coimbra, 3000-548, Portugal.
Maria do Céu SousaFaculty of Pharmacy, University of Coimbra, Coimbra, 3000-548, Portugal.
Fernanda A RosaChemistry Department, State University of Maringá, Maringa, 87020-900, Brazil.
Andrey P JacominiChemistry Department, State University of Maringá, Maringa, 87020-900, Brazil.
Sueli O SilvaLaboratório de Inovação Tecnológica no Desenvolvimento de Fármacos e Cosméticos, State University of Maringá, Maringa, 87020-900, Brazil.
Tânia Ueda-NakamuraLaboratório de Inovação Tecnológica no Desenvolvimento de Fármacos e Cosméticos, State University of Maringá, Maringa, 87020-900, Brazil.
Adley F RubiraChemistry Department, State University of Maringá, Maringa, 87020-900, Brazil.
Celso V NakamuraLaboratório de Inovação Tecnológica no Desenvolvimento de Fármacos e Cosméticos, State University of Maringá, Maringa, 87020-900, Brazil. cvnakamura@gmail.com.
Universidade Estadual de Maringá · BRUniversity of Coimbra · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Yeast cell wall particles isolated from Saccharomyces cerevisiae (scYCWPs) have a rich constitution of β-glucan derived from the cell wall. After removing intracellular contents, β-glucan molecules are readily recognized by dectin-1 receptors, present on the cytoplasmic membrane surface of the mononuclear phagocytic cells and internalized. Leishmania spp. are obligate intracellular parasites; macrophages are its primary host cells. An experimental murine model of visceral leishmaniasis caused by L. infantum was used to evaluate the antileishmanial activity of oral administration of these particles. A low-water soluble thiophene previously studied in vitro against L. infantum was entrapped into scYCWPs to direct it into the host cell, in order to circumvent the typical pharmacokinetic problems of water-insoluble compounds. We found that scYCWPs + T6 reduced the parasitic burden in the liver and spleen. There was an increase in IFN-γ levels related to nitric oxide production, explaining the reduction of the L. infantum burden in the tissue. Histological analysis did not show signals of tissue inflammation and biochemical analysis from plasma did not indicate signals of cytotoxicity after scYCWPs + T6 treatment. These findings suggested that scYCWPs + T6 administered through oral route reduced the parasitic burden without causing toxic effects, satisfying requirements for development of new strategies to treat leishmaniasis.

Indexed as

Administration, OralAnimalsAntiprotozoal AgentsCell WallDisease Models, AnimalLeishmaniasis, VisceralMiceMice, Inbred BALB CParasitemiaSaccharomyces cerevisiaeAntiprotozoal Agents

Identifiers

PMID31882925
PMCPMC6934808
OpenAlexW2997497639

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.