Evidence map›Paper›PMID 24771856›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

An increase in tolerogenic dendritic cell and natural regulatory T cell numbers during experimental autoimmune encephalomyelitis in Rras-/- mice results in attenuated disease.

Avijit Ray, Sreemanti Basu, Nichole M Miller, Andrew M Chan, Bonnie N Dittel

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-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

14 citing papers in PubMed, 19 citations in OpenAlex.

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  7. R-Ras1 and R-Ras2 Are Essential for Oligodendrocyte Differentiation and Survival for Correct Myelination in the Central Nervous System.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    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

5 authors at 2 institutions in 1 country.

Avijit RayBlood Research Institute, BloodCenter of Wisconsin, Milwaukee, WI 53201;
Sreemanti BasuBlood Research Institute, BloodCenter of Wisconsin, Milwaukee, WI 53201; Department of Microbiology and Molecular Genetics, Medical College of Wisconsin, Milwaukee, WI 53226; and.
Nichole M MillerBlood Research Institute, BloodCenter of Wisconsin, Milwaukee, WI 53201;
Andrew M ChanDivision of Hematology and Oncology, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI 53226.
Bonnie N DittelBlood Research Institute, BloodCenter of Wisconsin, Milwaukee, WI 53201; Department of Microbiology and Molecular Genetics, Medical College of Wisconsin, Milwaukee, WI 53226; and bonnie.dittel@bcw.edu.
Versiti Blood Center of Wisconsin · USMedical College of Wisconsin · US

Funding

The Role of B Cells in Regulating AutoimmunityR01AI069358 · NIAID · VERSITI WISCONSIN, INC. · PI DITTEL, BONNIE N · 2008 to 2012
$2.0M
Mechanisms of Regulatory B Cell FunctionR56AI106672 · NIAID · VERSITI WISCONSIN, INC. · PI DITTEL, BONNIE N · 2013 to 2013
$392k
NIAID NIH HHS R01 AI069358NIAID NIH HHS R56 AI106672
6 · The paper itself

Abstract

R-Ras is a member of the Ras superfamily of small GTPases, which are regulators of various cellular processes, including adhesion, survival, proliferation, trafficking, and cytokine production. R-Ras is expressed by immune cells and has been shown to modulate dendritic cell (DC) function in vitro and has been associated with liver autoimmunity. We used Rras-deficient mice to study the mechanism whereby R-Ras contributes to autoimmunity using experimental autoimmune encephalomyelitis (EAE), a mouse model of the CNS autoimmune disease multiple sclerosis. We found that a lack of R-Ras in peripheral immune cells resulted in attenuated EAE disease. Further investigation revealed that, during EAE, absence of R-Ras promoted the formation of MHC II(low) DC concomitant with a significant increase in proliferation of natural regulatory T cells, resulting in an increase in their cell numbers in the periphery. Our study suggests a novel role for R-Ras in promoting autoimmunity through negative regulation of natural regulatory T cell numbers by inhibiting the development of MHCII(low) DC with tolerogenic potential.

Indexed as

Immune ToleranceAnimalsDendritic CellsEncephalomyelitis, Autoimmune, ExperimentalHistocompatibility Antigens Class IIMiceMice, KnockoutMultiple Sclerosisras ProteinsT-Lymphocytes, RegulatoryHistocompatibility Antigens Class IIras ProteinsRras protein, mouse

Identifiers

PMID24771856
PMCPMC4041102
OpenAlexW1899891922

What OpenQuestion holds

Textmetadata
LicenceTDM
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.