Evidence map›Paper›PMID 32811567›Full record

ArticleActa neuropathologica communications2020

Single-cell mass cytometry reveals complex myeloid cell composition in active lesions of progressive multiple sclerosis.

Chotima Böttcher, Marlijn van der Poel, Camila Fernández-Zapata, Stephan Schlickeiser, Julia K H Leman, Cheng-Chih Hsiao, Mark R Mizee, Adelia, Maria C J Vincenten, Desiree Kunkel and 3 more

Open access · goldAbstract read
In one paragraph

Article in Acta neuropathologica communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 6% 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, 1 synthesis or guideline pooled it, 56 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

13 authors at 4 institutions in 3 countries.

Chotima BöttcherDepartment of Neuropsychiatry and Laboratory of Molecular Psychiatry, Charité - Universitätsmedizin Berlin, Berlin, Germany. chotima.boettcher@charite.de.ORCID 0000-0002-6226-586X
Marlijn van der PoelNeuroimmunology Research Group, Netherlands Institute for Neuroscience, Amsterdam, The Netherlands.
Camila Fernández-ZapataDepartment of Neuropsychiatry and Laboratory of Molecular Psychiatry, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Stephan SchlickeiserBIH Center for Regenerative Therapies (BCRT), Charité - Universitätsmedizin Berlin, Berlin, Germany.
Julia K H LemanDepartment of Neuropsychiatry and Laboratory of Molecular Psychiatry, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Cheng-Chih HsiaoNeuroimmunology Research Group, Netherlands Institute for Neuroscience, Amsterdam, The Netherlands.
Mark R MizeeNeuroimmunology Research Group, Netherlands Institute for Neuroscience, Amsterdam, The Netherlands.
AdeliaNetherlands Brain Bank, Netherlands Institute for Neuroscience, Amsterdam, The Netherlands.
Maria C J VincentenNeuroimmunology Research Group, Netherlands Institute for Neuroscience, Amsterdam, The Netherlands.
Desiree KunkelFlow & Mass Cytometry Core Facility, Charité - Universitätsmedizin Berlin and Berlin Institute of Health (BIH), Berlin, Germany.
Inge HuitingaNeuroimmunology Research Group, Netherlands Institute for Neuroscience, Amsterdam, The Netherlands.
Jörg HamannNeuroimmunology Research Group, Netherlands Institute for Neuroscience, Amsterdam, The Netherlands.
Josef PrillerDepartment of Neuropsychiatry and Laboratory of Molecular Psychiatry, Charité - Universitätsmedizin Berlin, Berlin, Germany. josef.priller@charite.de.
Netherlands Institute for Neuroscience · NLCharité - Universitätsmedizin Berlin · DEBerlin Institute of Health at Charité - Universitätsmedizin Berlin · DEGerman Center for Neurodegenerative Diseases · DE

Funding

Medical Research Council MC_PC_16031
6 · The paper itself

Abstract

Myeloid cells contribute to inflammation and demyelination in the early stages of multiple sclerosis (MS), but it is still unclear to what extent these cells are involved in active lesion formation in progressive MS (PMS). Here, we have harnessed the power of single-cell mass cytometry (CyTOF) to compare myeloid cell phenotypes in active lesions of PMS donors with those in normal-appearing white matter from the same donors and control white matter from non-MS donors. CyTOF measurements of a total of 74 targeted proteins revealed a decreased abundance of homeostatic and TNF

Indexed as

MicrogliaMyeloid CellsBrainCell SeparationFlow CytometryHumansMultiple Sclerosis, Chronic ProgressiveSingle-Cell AnalysisActive lesionMass cytometryMicrogliaMyeloid cellsProgressive multiple sclerosis

Identifiers

PMID32811567
PMCPMC7437178
OpenAlexW3060060316

What OpenQuestion holds

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Registered trials

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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.