Evidence map›Paper›PMID 27619998›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

IFN-β Facilitates Neuroantigen-Dependent Induction of CD25+ FOXP3+ Regulatory T Cells That Suppress Experimental Autoimmune Encephalomyelitis.

Duncheng Wang, Debjani Ghosh, S M Touhidul Islam, Cody D Moorman, Ashton E Thomason, Daniel S Wilkinson, Mark D Mannie

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

19 citing papers in PubMed, 26 citations in OpenAlex.

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  13. Human CommensalFrontiers in immunology · 2020
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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

7 authors at 1 institution in 1 country.

Duncheng WangDepartment of Microbiology and Immunology, Brody School of Medicine, East Carolina University, Greenville, NC 27834; and.ORCID 0000-0002-2085-9512
Debjani GhoshDepartment of Microbiology and Immunology, Brody School of Medicine, East Carolina University, Greenville, NC 27834; and.
S M Touhidul IslamDepartment of Microbiology and Immunology, Brody School of Medicine, East Carolina University, Greenville, NC 27834; and.ORCID 0000-0003-2720-4102
Cody D MoormanDepartment of Microbiology and Immunology, Brody School of Medicine, East Carolina University, Greenville, NC 27834; and.
Ashton E ThomasonDepartment of Microbiology and Immunology, Brody School of Medicine, East Carolina University, Greenville, NC 27834; and.
Daniel S WilkinsonDepartment of Microbiology and Immunology, Brody School of Medicine, East Carolina University, Greenville, NC 27834; and.
Mark D MannieDepartment of Microbiology and Immunology, Brody School of Medicine, East Carolina University, Greenville, NC 27834; and manniem@ecu.edu.ORCID 0000-0003-0475-8516
East Carolina University · US

Funding

Interferon-beta as an Adjuvant for Tolerogenic VaccinationR01AI126398 · NIAID · EAST CAROLINA UNIVERSITY · PI MANNIE, MARK D. · 2016 to 2020
$2.1M
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
NIAID NIH HHS R01 AI126398NINDS NIH HHS R01 NS072150NINDS NIH HHS R15 NS075830
6 · The paper itself

Abstract

This study introduces a flexible format for tolerogenic vaccination that incorporates IFN-β and neuroantigen (NAg) in the Alum adjuvant. Tolerogenic vaccination required all three components, IFN-β, NAg, and Alum, for inhibition of experimental autoimmune encephalomyelitis (EAE) and induction of tolerance. Vaccination with IFN-β + NAg in Alum ameliorated NAg-specific sensitization and inhibited EAE in C57BL/6 mice in pretreatment and therapeutic regimens. Tolerance induction was specific for the tolerogenic vaccine Ag PLP178-191 or myelin oligodendrocyte glycoprotein (MOG)35-55 in proteolipid protein- and MOG-induced models of EAE, respectively, and was abrogated by pretreatment with a depleting anti-CD25 mAb. IFN-β/Alum-based vaccination exhibited hallmarks of infectious tolerance, because IFN-β + OVA in Alum-specific vaccination inhibited EAE elicited by OVA + MOG in CFA but not EAE elicited by MOG in CFA. IFN-β + NAg in Alum vaccination elicited elevated numbers and percentages of FOXP3

Indexed as

Adjuvants, ImmunologicAlum CompoundsAnimalsBystander EffectCells, CulturedEncephalomyelitis, Autoimmune, ExperimentalForkhead Transcription FactorsHumansImmune ToleranceInterferon-betaInterleukin-2 Receptor alpha SubunitMiceMice, Inbred C57BLMice, TransgenicMultiple SclerosisMyelin-Oligodendrocyte GlycoproteinAdjuvants, ImmunologicAlum Compoundsaluminum sulfateForkhead Transcription FactorsFoxp3 protein, mouseInterferon-betaInterleukin-2 Receptor alpha SubunitMyelin-Oligodendrocyte Glycoproteinmyelin oligodendrocyte glycoprotein (35-55)Myelin Proteolipid Proteinmyelin proteolipid protein (178-191)Peptide FragmentsVaccines

Identifiers

PMID27619998
PMCPMC5101178
OpenAlexW2528229375

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.