Evidence map›Paper›PMID 25241937›Full record

ReviewTranslational research : the journal of laboratory and clinical medicine2015

The meninges: new therapeutic targets for multiple sclerosis.

Abigail E Russi, Melissa A Brown

Open access · bronzeAbstract readReview
In one paragraph

Review in Translational research : the journal of laboratory and clinical medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 87 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Meninges: A Widespread Niche of Neural Progenitors for the Brain.The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry · 2021
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Mast cells and angiogenesis in multiple sclerosis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2020
    Review
  20. Review
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

2 authors at 1 institution in 1 country.

Abigail E RussiDepartment of Microbiology and Immunology, Northwestern University Feinberg School of Medicine, Chicago, Ill.
Melissa A BrownDepartment of Microbiology and Immunology, Northwestern University Feinberg School of Medicine, Chicago, Ill. Electronic address: m-brown12@northwestern.edu.
Northwestern University · US

Funding

Mechanisms of mast cell influence on EAE disease courseR01NS047578 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BROWN, MELISSA A · 2006 to 2010
$1.6M
Mechanisms Regulating Reduced c-Kit-Dependent EAE Susceptibility in Male SJL MiceR21NS081598 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BROWN, MELISSA A · 2012 to 2013
$418k
Mast cells' contribution to T cell immunityR56AI064769 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BROWN, MELISSA ANN · 2007 to 2007
$378k
C-kit Signaling Pathways Regulate EAE Susceptibility in Male SJL MiceF31NS084691 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SHORT, ABIGAIL ELIZABETH · 2013 to 2015
$143k
NIAID NIH HHS R56 AI064769NINDS NIH HHS F31 NS084691NINDS NIH HHS F31 NS084691-02NINDS NIH HHS R01 NS047578NINDS NIH HHS R01NS047578NINDS NIH HHS R21 NS081598NINDS NIH HHS R21NS081598
6 · The paper itself

Abstract

The central nervous system (CNS) largely comprises nonregenerating cells, including neurons and myelin-producing oligodendrocytes, which are particularly vulnerable to immune cell-mediated damage. To protect the CNS, mechanisms exist that normally restrict the transit of peripheral immune cells into the brain and spinal cord, conferring an "immune-specialized" status. Thus, there has been a long-standing debate as to how these restrictions are overcome in several inflammatory diseases of the CNS, including multiple sclerosis (MS). In this review, we highlight the role of the meninges, tissues that surround and protect the CNS and enclose the cerebral spinal fluid, in promoting chronic inflammation that leads to neuronal damage. Although the meninges have traditionally been considered structures that provide physical protection for the brain and spinal cord, new data have established these tissues as sites of active immunity. It has been hypothesized that the meninges are important players in normal immunosurveillance of the CNS but also serve as initial sites of anti-myelin immune responses. The resulting robust meningeal inflammation elicits loss of localized blood-brain barrier (BBB) integrity and facilitates a large-scale influx of immune cells into the CNS parenchyma. We propose that targeting the cells and molecules mediating these inflammatory responses within the meninges offers promising therapies for MS that are free from the constraints imposed by the BBB. Importantly, such therapies may avoid the systemic immunosuppression often associated with the existing treatments.

Indexed as

AnimalsAntibodies, MonoclonalBlood-Brain BarrierBrainEncephalomyelitis, Autoimmune, ExperimentalHumansInflammationMast CellsMeningesMiceModels, ImmunologicalMultiple SclerosisNeutrophil InfiltrationT-LymphocytesTranslational Research, BiomedicalAntibodies, Monoclonal

Identifiers

PMID25241937
PMCPMC4424790
OpenAlexW2081102318

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.