Evidence map›Paper›PMID 17900707›Full record

ReviewJournal of neuroimmunology2007

Control of experimental autoimmune encephalomyelitis by CD4+ suppressor T cells: peripheral versus in situ immunoregulation.

Margaret S Bynoe, Paula Bonorino, Christophe Viret

Abstract readComparative StudyReview
In one paragraph

Review in Journal of neuroimmunology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
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

3 authors.

Margaret S BynoeDepartment of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, New York 14850, USA. msb76@cornell.edu
Paula Bonorino
Christophe Viret

Funding

Tolerance induction in EAE by epicutaneous immunizationK22AI057854 · NIAID · CORNELL UNIVERSITY ITHACA · PI BYNOE, MARGARET S · 2005 to 2006
$268k
NIAID NIH HHS AI57854NIAID NIH HHS K22 AI057854
6 · The paper itself

Abstract

The pathogenesis of experimental autoimmune encephalomyelitis (EAE) can be efficiently kept under control by specialized subsets of CD4+ T lymphocytes able to negatively regulate the function of T cells with encephalitogenic potential. A number of observations support a role for such suppressor T cells in controlling early phases of disease development at the level of peripheral lymphoid organs but there is also evidence suggesting immunoregulation within the central nervous system (CNS) microenvironment itself. This review evaluates the sites of regulation based on available data from distinct experimental models. We then discuss these aspects with reference to suppressor CD4+ T cells induced through the epicutaneous application of pure CNS antigens that confer long term protection against EAE. Finally, we give an overview of genes recently discovered to be important in regulation of the immune system that may also prove to be key players in the modulation of EAE and MS.

Indexed as

AnimalsBrainCD4-Positive T-LymphocytesEncephalomyelitis, Autoimmune, ExperimentalGlycoproteinsHumansImmunizationInterleukin-17Interleukin-23Multiple SclerosisMyelin-Oligodendrocyte GlycoproteinPeptide FragmentsT-Lymphocytes, RegulatoryGlycoproteinsInterleukin-17Interleukin-23Myelin-Oligodendrocyte Glycoproteinmyelin oligodendrocyte glycoprotein (35-55)Peptide Fragments

Identifiers

PMID17900707
PMCPMC2117378

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.