Evidence map›Paper›PMID 27256565›Full record

ArticleJournal of leukocyte biology2016

Depletion of CD4+ CD25+ regulatory T cells confers susceptibility to experimental autoimmune encephalomyelitis (EAE) in GM-CSF-deficient Csf2-/- mice.

Debjani Ghosh, Alan D Curtis, Daniel S Wilkinson, Mark D Mannie

Abstract read
In one paragraph

Article in Journal of leukocyte biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

Debjani GhoshDepartment of Microbiology and Immunology, Brody School of Medicine, East Carolina University, Greenville, North Carolina, USA; and.
Alan D CurtisDepartment of Microbiology and Immunology, Brody School of Medicine, East Carolina University, Greenville, North Carolina, USA; and.
Daniel S WilkinsonDepartment of Microbiology and Immunology, Brody School of Medicine, East Carolina University, Greenville, North Carolina, USA; and.
Mark D MannieDepartment of Microbiology and Immunology, Brody School of Medicine, East Carolina University, Greenville, North Carolina, USA; and The Harriet and John Wooten Laboratory for Alzheimer's and Neurodegenerative Disease Research, Brody School of Medicine, East Carolina University, Greenville, North Carolina, USA manniem@ecu.edu.
East Carolina University · US

Funding

Interferons as adjuvants for tolerogenic vaccinesR01NS072150 · NINDS · EAST CAROLINA UNIVERSITY · PI MANNIE, MARK D. · 2011 to 2015
$1.5M
Therapeutic vaccines for treatment of experimental autoimmune encephalomyelitis (R15NS075830 · NINDS · EAST CAROLINA UNIVERSITY · PI MANNIE, MARK D. · 2011 to 2011
$429k
NINDS NIH HHS R01 NS072150NINDS NIH HHS R15 NS075830
6 · The paper itself

Abstract

Previous studies established that GM-CSF-deficient (Csf2-deficient) mice exhibit profound resistance to experimental autoimmune encephalomyelitis. This study addressed whether the resistance of Csf2-deficient mice was a result of a requirement for GM-CSF in controlling the functional balance between effector and regulatory T cell subsets during experimental autoimmune encephalomyelitis. The main observation was that treatment with the anti-CD25 mAb PC61 rendered Csf2-deficient mice fully susceptible to severe, chronic experimental autoimmune encephalomyelitis, with disease incidences and severities equivalent to that of C57BL/6 mice. When both donors and recipients were treated with PC61 in a passive model of experimental autoimmune encephalomyelitis, adoptive transfer of myelin-specific Csf2-deficient T cells into Csf2-deficient recipients resulted in a nonresolving chronic course of severe paralytic experimental autoimmune encephalomyelitis. The peripheral Csf2-deficient T cell repertoire was marked by elevated CD3

Indexed as

Lymphocyte DepletionAdoptive TransferAnimalsAntibodies, MonoclonalCD4-Positive T-LymphocytesDisease SusceptibilityEncephalomyelitis, Autoimmune, ExperimentalGranulocyte-Macrophage Colony-Stimulating FactorGranulocytesImmunophenotypingInterleukin-2 Receptor alpha SubunitLeukocyte CountLymphocyte CountMiceMice, Inbred C57BLMyelin-Oligodendrocyte GlycoproteinAntibodies, MonoclonalGranulocyte-Macrophage Colony-Stimulating FactorInterleukin-2 Receptor alpha SubunitMyelin-Oligodendrocyte Glycoproteinmyelin oligodendrocyte glycoprotein (35-55)Peptide FragmentsFOXP3+ T cellsmultiple sclerosisneuroimmunologytolerance

Identifiers

PMID27256565
PMCPMC5014742
OpenAlexW2411228224

What OpenQuestion holds

Textmetadata
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.