Evidence map›Paper›PMID 31191554›Full record

ArticleFrontiers in immunology2019

Glucocorticoid Therapy of Multiple Sclerosis Patients Induces Anti-inflammatory Polarization and Increased Chemotaxis of Monocytes.

Henrike J Fischer, Tobias L K Finck, Hannah L Pellkofer, Holger M Reichardt, Fred Lühder

Open access · goldAbstract readComparative Study
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
1.6field-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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 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

5 authors at 1 institution in 1 country.

Henrike J FischerInstitute for Neuroimmunology and Multiple Sclerosis Research, University Medical Center Goettingen, Göttingen, Germany.
Tobias L K FinckInstitute for Neuroimmunology and Multiple Sclerosis Research, University Medical Center Goettingen, Göttingen, Germany.
Hannah L PellkoferDepartment of Neurology, University Medical Center Goettingen, Göttingen, Germany.
Holger M ReichardtInstitute for Cellular and Molecular Immunology, University Medical Center Goettingen, Göttingen, Germany.
Fred LühderInstitute for Neuroimmunology and Multiple Sclerosis Research, University Medical Center Goettingen, Göttingen, Germany.
University of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple Sclerosis (MS) is an autoimmune disease of the central nervous system (CNS), characterized by the infiltration of mononuclear cells into the CNS and a subsequent inflammation of the brain. Monocytes are implicated in disease pathogenesis not only in their function as potential antigen-presenting cells involved in the local reactivation of encephalitogenic T cells but also by independent effector functions contributing to structural damage and disease progression. However, monocytes also have beneficial effects as they can exert anti-inflammatory activity and promote tissue repair. Glucocorticoids (GCs) are widely used to treat acute relapses in MS patients. They act on a variety of cell types but their exact mechanisms of action including their modulation of monocyte function are not fully understood. Here we investigated effects of the therapeutically relevant GC methylprednisolone (MP) on monocytes from healthy individuals and MS patients

Indexed as

AdultAgedAntigens, CDAntigens, Differentiation, MyelomonocyticAnti-Inflammatory AgentsCD163 AntigenChemokine CCL2Chemotaxis, LeukocyteFemaleHumansMaleMethylprednisoloneMiddle AgedMonocytesMultiple Sclerosis, Chronic ProgressiveMultiple Sclerosis, Relapsing-RemittingAntigens, CDAntigens, Differentiation, MyelomonocyticAnti-Inflammatory AgentsCCL2 protein, humanCCR2 protein, humanCD163 AntigenChemokine CCL2MethylprednisoloneNR3C1 protein, humanReceptors, CCR2Receptors, Cell SurfaceReceptors, GlucocorticoidchemokinesM2 polarizationmethylprednisolone therapymonocytesmultiple sclerosis

Identifiers

PMID31191554
PMCPMC6549240
OpenAlexW2947976783

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.