Evidence map›Paper›PMID 28941240›Full record

ArticleStem cells translational medicine2017

Dynamic Changes in Brain Mesenchymal Perivascular Cells Associate with Multiple Sclerosis Disease Duration, Active Inflammation, and Demyelination.

Ellen Iacobaeus, Rachael V Sugars, Anton Törnqvist Andrén, Jessica J Alm, Hong Qian, Janek Frantzen, Jia Newcombe, Kanar Alkass, Henrik Druid, Matteo Bottai and 2 more

Open access · goldAbstract read
In one paragraph

Article in Stem cells translational medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 16% 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

23 citing papers in PubMed, 44 citations in OpenAlex.

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  9. Towards a Unified Approach in Autoimmune Fibrotic Signalling Pathways.International journal of molecular sciences · 2023
    Review
  10. Article
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  12. CNS Pericytes Modulate Local T Cell Infiltration in EAE.International journal of molecular sciences · 2022
    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

12 authors at 10 institutions in 5 countries.

Ellen IacobaeusDivision of Clinical Immunology, Department of Laboratory Medicine, Finland.ORCID 0000-0001-7832-8215
Rachael V SugarsDivision of Oral Facial Diagnostics and Surgery, Department of Dental Medicine, Finland.
Anton Törnqvist AndrénDivision of Clinical Immunology, Department of Laboratory Medicine, Finland.
Jessica J AlmDivision of Clinical Immunology, Department of Laboratory Medicine, Finland.
Hong QianCenter for Hematology and Regenerative Medicine, Department of Medicine, Stockholm, Sweden.
Janek FrantzenDivision of Clinical Neuroscience, Department of Neurosurgery, University of Turku and Turku University Hospital, Finland.
Jia NewcombeNeuroResource, UCL Institute of Neurology, University College London, London, England, United Kingdom.
Kanar AlkassKI Donatum, Department of Forensic Medicine, Stockholm, Sweden.
Henrik DruidKI Donatum, Department of Forensic Medicine, Stockholm, Sweden.
Matteo BottaiUnit of Biostatistics, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Matias RöyttäDepartment of Pathology, University of Turku and Turku University Hospital, Finland.
Katarina Le BlancDivision of Clinical Immunology, Department of Laboratory Medicine, Finland.
358 (Finland) · FISwedish National Board of Forensic Medicine · SECenter for Neuroscience and Regenerative Medicine · USCenter for Neurosciences · USCS Diagnostics · DEKarolinska Institutet · SEKarolinska University Hospital · SETurku University Hospital · FIUniversity College London · GBUniversity of Turku · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vascular changes, including blood brain barrier destabilization, are common pathological features in multiple sclerosis (MS) lesions. Blood vessels within adult organs are reported to harbor mesenchymal stromal cells (MSCs) with phenotypical and functional characteristics similar to pericytes. We performed an immunohistochemical study of MSCs/pericytes in brain tissue from MS and healthy persons. Post-mortem brain tissue from patients with early progressive MS (EPMS), late stage progressive MS (LPMS), and healthy persons were analyzed for the MSC and pericyte markers CD146, platelet-derived growth factor receptor beta (PDGFRβ), CD73, CD271, alpha-smooth muscle actin, and Ki67. The MS samples included active, chronic active, chronic inactive lesions, and normal-appearing white matter. MSC and pericyte marker localization were detected in association with blood vessels, including subendothelial CD146

Indexed as

5'-NucleotidaseAdultAgedAged, 80 and overBlood VesselsBrainCD146 AntigenFemaleHumansKi-67 AntigenMaleMesenchymal Stem CellsMiddle AgedMultiple SclerosisMyelin SheathNerve Tissue Proteins5'-NucleotidaseCD146 AntigenKi-67 AntigenNerve Tissue ProteinsNGFR protein, humanReceptor, Platelet-Derived Growth Factor betaReceptors, Nerve Growth FactorBlood vesselsCentral nervous systemMesenchymal stromal cellMultiple sclerosisNeuroinflammationPericytePerivascular niche

Identifiers

PMID28941240
PMCPMC6430046
OpenAlexW2759269620

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.