Evidence map›Paper›PMID 29178933›Full record

ArticleActa neuropathologica communications2017

The chronically inflamed central nervous system provides niches for long-lived plasma cells.

Karolin Pollok, Ronja Mothes, Carolin Ulbricht, Alina Liebheit, Jan David Gerken, Sylvia Uhlmann, Friedemann Paul, Raluca Niesner, Helena Radbruch, Anja Erika Hauser

Open access · goldAbstract read
In one paragraph

Article in Acta neuropathologica communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

41 citing papers in PubMed, 67 citations in OpenAlex.

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  19. NAIR: Network Analysis of Immune Repertoire.Frontiers in immunology · 2023
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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

10 authors at 3 institutions in 1 country.

Karolin PollokCharité - Universitätsmedizin Berlin, Immune Dynamics and Intravital Microscopy, 10117 Berlin, Germany.
Ronja MothesCharité - Universitätsmedizin Berlin, Immune Dynamics and Intravital Microscopy, 10117 Berlin, Germany.
Carolin UlbrichtCharité - Universitätsmedizin Berlin, Immune Dynamics and Intravital Microscopy, 10117 Berlin, Germany.
Alina LiebheitCharité - Universitätsmedizin Berlin, Immune Dynamics and Intravital Microscopy, 10117 Berlin, Germany.
Jan David GerkenCharité - Universitätsmedizin Berlin, Immune Dynamics and Intravital Microscopy, 10117 Berlin, Germany.
Sylvia UhlmannCharité - Universitätsmedizin Berlin, Immune Dynamics and Intravital Microscopy, 10117 Berlin, Germany.
Friedemann PaulCharité - Universitätsmedizin Berlin, Experimental and Clinical Research Center and Clinical and Experimental Multiple Sclerosis Research Center, Department of Neurology, and Max Delbrück Center for Molecular Medicine, Berlin, Germany.
Raluca NiesnerDeutsches Rheuma-Forschungszentrum Berlin, a Leibniz Institute, Biophysical Analytics, 10117 Berlin, Germany.
Helena RadbruchDept. of Neuropathology Charité - Universitätsmedizin Berlin, Charitéplatz 1, 10117, Berlin, Germany. helena.radbruch@charite.de.
Anja Erika HauserCharité - Universitätsmedizin Berlin, Immune Dynamics and Intravital Microscopy, 10117 Berlin, Germany. anja.hauser-hankeln@charite.de.
Charité - Universitätsmedizin Berlin · DEGerman Rheumatism Research Centre · DEMax Delbrück Center · DE

Funding

Berlin Institute of Health Doctoral scholarshipDeutsche Forschungsgemeinschaft EXC 257 NeuroCureDeutsche Forschungsgemeinschaft TRR130, C01Deutsche Forschungsgemeinschaft TRR130, TP17Novartis Foundation Unconditional grant
6 · The paper itself

Abstract

Although oligoclonal bands in the cerebrospinal fluid have been a hallmark of multiple sclerosis diagnosis for over three decades, the role of antibody-secreting cells in multiple sclerosis remains unclear. T and B cells are critical for multiple sclerosis pathogenesis, but increasing evidence suggests that plasma cells also contribute, through secretion of autoantibodies. Long-lived plasma cells are known to drive various chronic inflammatory conditions as e.g. systemic lupus erythematosus, however, to what extent they are present in autoimmune central nervous system inflammation has not yet been investigated. In brain biopsies from multiple sclerosis patients and other neurological diseases, we could detect non-proliferating plasma cells (CD138

Indexed as

AdultAgedAnimalsAntigens, CDCalcium-Binding ProteinsChemokine CXCL12Disease Models, AnimalDNA-Binding ProteinsEncephalomyelitis, Autoimmune, ExperimentalFemaleFlow CytometryGlial Fibrillary Acidic ProteinHumansKi-67 AntigenMaleMiceAIF1 protein, humanAntigens, CDCalcium-Binding ProteinsChemokine CXCL12DNA-Binding ProteinsGlial Fibrillary Acidic ProteinKi-67 AntigenMicrofilament ProteinsVascular Cell Adhesion Molecule-1B cellsExperimental autoimmune encephalomyelitisMultiple sclerosisPlasma cells

Identifiers

PMID29178933
PMCPMC5702095
OpenAlexW2770244745

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.