Evidence map›Paper›PMID 24463292›Full record

ArticleInternational journal of molecular sciences2014

Regulation of an autoimmune model for multiple sclerosis in Th2-biased GATA3 transgenic mice.

Viromi Fernando, Seiichi Omura, Fumitaka Sato, Eiichiro Kawai, Nicholas E Martinez, Sadie Faith Elliott, Keigyou Yoh, Satoru Takahashi, Ikuo Tsunoda

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

30 citing papers in PubMed, 50 citations in OpenAlex.

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  15. Immunoregulatory Effects of Tolerogenic Probiotics in Multiple Sclerosis.Advances in experimental medicine and biology · 2021
    Review
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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

9 authors at 2 institutions in 2 countries.

Viromi FernandoDepartment of Microbiology and Immunology, Center for Tumor and Molecular Virology, Louisiana State University Health Sciences Center, Shreveport, LA 71130, USA. viromi.fernando@gmail.com.
Seiichi OmuraDepartment of Microbiology and Immunology, Center for Tumor and Molecular Virology, Louisiana State University Health Sciences Center, Shreveport, LA 71130, USA. omura.s@hotmail.com.
Fumitaka SatoDepartment of Microbiology and Immunology, Center for Tumor and Molecular Virology, Louisiana State University Health Sciences Center, Shreveport, LA 71130, USA. fsato@lsuhsc.edu.
Eiichiro KawaiDepartment of Microbiology and Immunology, Center for Tumor and Molecular Virology, Louisiana State University Health Sciences Center, Shreveport, LA 71130, USA. ekawai-thk@umin.ac.jp.
Nicholas E MartinezDepartment of Microbiology and Immunology, Center for Tumor and Molecular Virology, Louisiana State University Health Sciences Center, Shreveport, LA 71130, USA. nmarti@lsuhsc.edu.
Sadie Faith ElliottDepartment of Microbiology and Immunology, Center for Tumor and Molecular Virology, Louisiana State University Health Sciences Center, Shreveport, LA 71130, USA. Iloveham2011@yahoo.com.
Keigyou YohDepartment of Nephrology, Division of Clinical Medicine, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki 305-8575, Japan. k-yohnpr@umin.ac.jp.
Satoru TakahashiDepartment of Anatomy and Embryology, Faculty of Medicine, International Institute for Integrative Sleep Medicine (WPI-IIIS), Life Science Center, Tsukuba Research Alliance (TARA), Laboratory Animal Resource Center (LARC), University of Tsukuba, 1-1-1 Tennoudai, Tsukuba, Ibaraki 305-8575, Japan. satoruta@md.tsukuba.ac.jp.
Ikuo TsunodaDepartment of Microbiology and Immunology, Center for Tumor and Molecular Virology, Louisiana State University Health Sciences Center, Shreveport, LA 71130, USA. itsuno@lsuhsc.edu.
Louisiana State University Health Sciences Center Shreveport · USUniversity of Tsukuba · JP

Funding

RECRUITMENT YEAR FOR PI#5P20RR018724 · NCRR · LOUISIANA STATE UNIV HSC SHREVEPORT · PI TSUNODA, IKUO · 2003 to 2011
$16.1M
COBRE Center for Molecular and Tumor VirologyP30GM110703 · NIGMS · LOUISIANA STATE UNIV HSC SHREVEPORT · PI SAPP, MARTIN · 2014 to 2018
$4.8M
COBRE Center for Molecular and Tumor VirologyP20GM103433 · NIGMS · LOUISIANA STATE UNIV HSC SHREVEPORT · PI O'CALLAGHAN, DENNIS JOHN · 2012 to 2012
$1.9M
Axonal degeneration can trigger demyelinating diseaseR21NS059724 · NINDS · UNIVERSITY OF UTAH · PI TSUNODA, IKUO · 2008 to 2009
$357k
NCRR NIH HHS 5P20RR018724NCRR NIH HHS P20 RR018724NIGMS NIH HHS 8P20GM103433NIGMS NIH HHS P20 GM103433NIGMS NIH HHS P30 GM110703NINDS NIH HHS R21 NS059724NINDS NIH HHS R21NS059724
6 · The paper itself

Abstract

T helper (Th)2 cells have been proposed to play a neuroprotective role in multiple sclerosis (MS). This is mainly based on "loss-of-function" studies in an animal model for MS, experimental autoimmune encephalomyelitis (EAE), using blocking antibodies against Th2 related cytokines, and knockout mice lacking Th2-related molecules. We tested whether an increase of Th2 responses ("gain-of-function" approach) could alter EAE, the approach of novel GATA binding protein 3 (GATA3)-transgenic (tg) mice that overexpress GATA3, a transcription factor required for Th2 differentiation. In EAE induced with myelin oligodendrocyte glycoprotein (MOG)35-55 peptide, GATA3-tg mice had a significantly delayed onset of disease and a less severe maximum clinical score, compared with wild-type C57BL/6 mice. Histologically, GATA3-tg mice had decreased levels of meningitis and demyelination in the spinal cord, and anti-inflammatory cytokine profiles immunologically, however both groups developed similar levels of MOG-specific lymphoproliferative responses. During the early stage, we detected higher levels of interleukin (IL)-4 and IL-10, with MOG and mitogen stimulation of regional lymph node cells in GATA3-tg mice. During the late stage, only mitogen stimulation induced higher IL-4 and lower interferon-γ and IL-17 production in GATA3-tg mice. These results suggest that a preexisting bias toward a Th2 immune response may reduce the severity of inflammatory demyelinating diseases, including MS.

Indexed as

AnimalsCD3 ComplexCytokinesDemyelinating DiseasesDisease Models, AnimalEncephalomyelitis, Autoimmune, ExperimentalFemaleGATA3 Transcription FactorLymphocyte ActivationMaleMiceMice, TransgenicMultiple SclerosisMutationMyelin-Oligodendrocyte GlycoproteinSpinal CordCD3 ComplexCytokinesGATA3 Transcription FactorMyelin-Oligodendrocyte Glycoprotein

Identifiers

PMID24463292
PMCPMC3958817
OpenAlexW2145521029

What OpenQuestion holds

Textmetadata
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.