Evidence map›Paper›PMID 26260055›Full record

ArticleMalaria journal2015

Effect of mushroom Agaricus blazei on immune response and development of experimental cerebral malaria.

Cynthia H Val, Fátima Brant, Aline S Miranda, Flávia G Rodrigues, Bruno C L Oliveira, Elândia A Santos, Diego R R Assis, Lísia Esper, Bruno C Silva, Milene A Rachid and 5 more

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

6 citing papers in PubMed, 19 citations in OpenAlex.

  1. Combinatorial chemistry & high throughput screening · 2026
    Article
  2. Review
  3. Review
  4. Review
  5. Frontiers in immunology · 2020
    Article
  6. 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

15 authors at 3 institutions in 2 countries.

Cynthia H ValDepartment of Biochemistry and Immunology, Institute of Biological Science, Federal University of Minas Gerais, Bloco O4, 190 Av. Antônio Carlos, 6627-Pampulha, Belo Horizonte, MG, 31270-901, Brazil. Cynthia_honorato7@yahoo.com.br.
Fátima BrantDepartment of Biochemistry and Immunology, Institute of Biological Science, Federal University of Minas Gerais, Bloco O4, 190 Av. Antônio Carlos, 6627-Pampulha, Belo Horizonte, MG, 31270-901, Brazil. fatimacbrant@gmail.com.
Aline S MirandaProgramme in Health Sciences: Infectious Diseases and Tropical Medicine, Medical School, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil. alines.miranda@hotmail.com.
Flávia G RodriguesDepartment of Biochemistry and Immunology, Institute of Biological Science, Federal University of Minas Gerais, Bloco O4, 190 Av. Antônio Carlos, 6627-Pampulha, Belo Horizonte, MG, 31270-901, Brazil. flarodri2007@gmail.com.
Bruno C L OliveiraDepartment of Biochemistry and Immunology, Institute of Biological Science, Federal University of Minas Gerais, Bloco O4, 190 Av. Antônio Carlos, 6627-Pampulha, Belo Horizonte, MG, 31270-901, Brazil. bcabraloliveira@yahoo.com.br.
Elândia A SantosDepartment of Biochemistry and Immunology, Institute of Biological Science, Federal University of Minas Gerais, Bloco O4, 190 Av. Antônio Carlos, 6627-Pampulha, Belo Horizonte, MG, 31270-901, Brazil. elandiaas@yahoo.com.br.
Diego R R AssisDepartment of Biochemistry and Immunology, Institute of Biological Science, Federal University of Minas Gerais, Bloco O4, 190 Av. Antônio Carlos, 6627-Pampulha, Belo Horizonte, MG, 31270-901, Brazil. assisdrr@gmail.com.
Lísia EsperDepartment of Biochemistry and Immunology, Institute of Biological Science, Federal University of Minas Gerais, Bloco O4, 190 Av. Antônio Carlos, 6627-Pampulha, Belo Horizonte, MG, 31270-901, Brazil. lisiaesper@gmail.com.
Bruno C SilvaDepartment of Pathology, Institute of Biological Science, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil. brunobiopsy@yahoo.com.br.
Milene A RachidDepartment of Pathology, Institute of Biological Science, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil. milenerachid@gmail.com.
Herbert B TanowitzDepartment of Pathology and Department of Medicine, Albert Einstein College of Medicine, Bronx, NY, USA. herbert.tanowitz@einstein.yu.edu.
Antônio L TeixeiraProgramme in Health Sciences: Infectious Diseases and Tropical Medicine, Medical School, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil. altexr@gmail.com.
Mauro M TeixeiraDepartment of Biochemistry and Immunology, Institute of Biological Science, Federal University of Minas Gerais, Bloco O4, 190 Av. Antônio Carlos, 6627-Pampulha, Belo Horizonte, MG, 31270-901, Brazil. mmtex.ufmg@gmail.com.
Wiliam C B RégisPrograma de Pós Graduação em Biologia de Vertebrados da Pontifícia Universidade Católica de Minas Gerais, Belo Horizonte, MG, Brazil. wregis@pucminas.br.
Fabiana S MachadoDepartment of Biochemistry and Immunology, Institute of Biological Science, Federal University of Minas Gerais, Bloco O4, 190 Av. Antônio Carlos, 6627-Pampulha, Belo Horizonte, MG, 31270-901, Brazil. machadofs@icb.ufmg.br.
Universidade Federal de Minas Gerais · BRAlbert Einstein College of Medicine · USPontifícia Universidade Católica de Minas Gerais · BR

Funding

T. cruzi: pathogenesis modulation by eicosanoidsR01AI076248 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI TANOWITZ, HERBERT BERNARD · 2008 to 2012
$2.3M
NIAID NIH HHS R01 AI076248
6 · The paper itself

Abstract

backgroundCerebral malaria (CM) is debilitating and sometimes fatal. Disease severity has been associated with poor treatment access, therapeutic complexity and drug resistance and, thus, alternative therapies are increasingly necessary. In this study, the effect of the administration of Agaricus blazei, a mushroom of Brazilian origin in a model of CM caused by Plasmodium berghei, strain ANKA, was investigated in mice.

methodsC57BL/6 mice were pre-treated with aqueous extract or fractions of A. blazei, or chloroquine, infected with P. berghei ANKA and then followed by daily administration of A. blazei or chloroquine. Parasitaemia, body weight, survival and clinical signs of the disease were evaluated periodically. The concentration of pro-and anti-inflammatory cytokines, histopathology and in vitro analyses were performed.

resultsMice treated with A. blazei aqueous extract or fraction C, that shows antioxidant activity, displayed lower parasitaemia, increased survival, reduced weight loss and protection against the development of CM. The administration of A. blazei resulted in reduced levels of TNF, IL-1β and IL-6 production when compared to untreated P. berghei-infected mice. Agaricus blazei (aqueous extract or fraction C) treated infected mice displayed reduction of brain lesions. Although chloroquine treatment reduced parasitaemia, there was increased production of proinflammatory cytokines and damage in the CNS not observed with A. blazei treatment. Moreover, the in vitro pretreatment of infected erythrocytes followed by in vivo infection resulted in lower parasitaemia, increased survival, and little evidence of clinical signs of disease.

conclusionsThis study strongly suggests that the administration of A. blazei (aqueous extract or fraction C) was effective in improving the consequences of CM in mice and may provide novel therapeutic strategies.

Indexed as

AgaricusAnimalsAnti-Inflammatory AgentsAntimalarialsBiological ProductsBrainCytokinesFemaleMalaria, CerebralMiceMice, Inbred C57BLAnti-Inflammatory AgentsAntimalarialsBiological ProductsCytokines

Identifiers

PMID26260055
PMCPMC4531523
OpenAlexW2140477552

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.