Evidence map›Paper›PMID 27294161›Full record

ArticleJournal of immunology research2016

Systemic Administration of Proteoglycan Protects BALB/c Retired Breeder Mice from Experimental Arthritis.

Larissa Lumi Watanabe Ishikawa, Priscila Maria Colavite, Thais Fernanda de Campos Fraga-Silva, Luiza Ayumi Nishiyama Mimura, Thais Graziela Donegá França, Sofia Fernanda Gonçalves Zorzella-Pezavento, Fernanda Chiuso-Minicucci, Larissa Doddi Marcolino, Camila Marques, Maura Rosane Valerio Ikoma and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of immunology research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 96% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 2 institutions in 1 country.

Larissa Lumi Watanabe IshikawaDepartment of Microbiology and Immunology, Institute of Biosciences of Botucatu, São Paulo State University (UNESP), 18618-689 Botucatu, SP, Brazil.
Priscila Maria ColaviteDepartment of Microbiology and Immunology, Institute of Biosciences of Botucatu, São Paulo State University (UNESP), 18618-689 Botucatu, SP, Brazil.
Thais Fernanda de Campos Fraga-SilvaDepartment of Microbiology and Immunology, Institute of Biosciences of Botucatu, São Paulo State University (UNESP), 18618-689 Botucatu, SP, Brazil.
Luiza Ayumi Nishiyama MimuraDepartment of Microbiology and Immunology, Institute of Biosciences of Botucatu, São Paulo State University (UNESP), 18618-689 Botucatu, SP, Brazil.
Thais Graziela Donegá FrançaDepartment of Microbiology and Immunology, Institute of Biosciences of Botucatu, São Paulo State University (UNESP), 18618-689 Botucatu, SP, Brazil.
Sofia Fernanda Gonçalves Zorzella-PezaventoDepartment of Microbiology and Immunology, Institute of Biosciences of Botucatu, São Paulo State University (UNESP), 18618-689 Botucatu, SP, Brazil.
Fernanda Chiuso-MinicucciDepartment of Microbiology and Immunology, Institute of Biosciences of Botucatu, São Paulo State University (UNESP), 18618-689 Botucatu, SP, Brazil.
Larissa Doddi MarcolinoDepartment of Pathology, Botucatu Medical School, 18618-970 Botucatu, SP, Brazil.
Camila MarquesLaboratory of Flow Cytometry, Amaral Carvalho Foundation, 17210-120 Jaú, SP, Brazil.
Maura Rosane Valerio IkomaLaboratory of Flow Cytometry, Amaral Carvalho Foundation, 17210-120 Jaú, SP, Brazil.
Alexandrina SartoriDepartment of Microbiology and Immunology, Institute of Biosciences of Botucatu, São Paulo State University (UNESP), 18618-689 Botucatu, SP, Brazil.
Universidade Estadual Paulista (Unesp) · BRHospital Amaral Carvalho · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study was undertaken to evaluate the prophylactic potential of proteoglycan (PG) administration in experimental arthritis. Female BALB/c retired breeder mice received two (2xPG50 and 2xPG100 groups) or three (3xPG50 group) intraperitoneal doses of bovine PG (50 μg or 100 μg) every three days. A week later the animals were submitted to arthritis induction by immunization with three i.p. doses of bovine PG associated with dimethyldioctadecylammonium bromide adjuvant at intervals of 21 days. Disease severity was daily assessed after the third dose by score evaluation. The 3xPG50 group showed significant reduction in prevalence and clinical scores. This protective effect was associated with lower production of IFN-γ and IL-17 and increased production of IL-5 and IL-10 by spleen cells restimulated in vitro with PG. Even though previous PG administration restrained dendritic cells maturation this procedure did not alter the frequency of regulatory Foxp3(+) T cells. Lower TNF-α and IL-6 levels and higher expression of ROR-γ and GATA-3 were detected in the paws of protected animals. A delayed-type hypersensitivity reaction confirmed specific tolerance induction. Taken together, these results indicate that previous PG inoculation determines a specific tolerogenic effect that is able to decrease severity of subsequently induced arthritis.

Indexed as

AnimalsArthritis, ExperimentalCell DifferentiationCytokinesDendritic CellsDisease Models, AnimalFemaleMiceMice, Inbred BALB CProtective AgentsProteoglycansSeverity of Illness IndexT-Lymphocytes, RegulatoryTranscription FactorsCytokinesProtective AgentsProteoglycansTranscription Factors

Identifiers

PMID27294161
PMCPMC4887641
OpenAlexW2403360148

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.