Evidence map›Paper›PMID 36418303›Full record

ArticleNature communications2022

Differential compartmentalization of myeloid cell phenotypes and responses towards the CNS in Alzheimer's disease.

Camila Fernández Zapata, Ginevra Giacomello, Eike J Spruth, Jinte Middeldorp, Gerardina Gallaccio, Adeline Dehlinger, Claudia Dames, Julia K H Leman, Roland E van Dijk, Andreas Meisel and 7 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 30 citations in OpenAlex.

  1. Immune-proteo-metabolomic changes link to Aβ and tau pathology in Alzheimer disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
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  8. Review
  9. Thinking outside the brain: Gut microbiome influence on innate immunity within neurodegenerative disease.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. 1,2-Current issues in molecular biology · 2023
    Article
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

17 authors at 6 institutions in 3 countries.

Camila Fernández ZapataExperimental and Clinical Research Center, a cooperation between the Max Delbrück Center for Molecular Medicine in the Helmholtz Association and Charité Universitätsmedizin Berlin, Berlin, 13125, Germany.ORCID 0000-0003-4795-6053
Ginevra GiacomelloInstitute of Pharmacy, Freie Universität Berlin, Berlin, 14195, Germany.ORCID 0000-0002-0914-4241
Eike J SpruthDepartment of Neuropsychiatry and Laboratory of Molecular Psychiatry, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, 10117, Germany.
Jinte MiddeldorpDepartment of Translational Neuroscience, University Medical Center Utrecht Brain Center, Utrecht University, 3584 CX, Utrecht, The Netherlands.
Gerardina GallaccioExperimental and Clinical Research Center, a cooperation between the Max Delbrück Center for Molecular Medicine in the Helmholtz Association and Charité Universitätsmedizin Berlin, Berlin, 13125, Germany.ORCID 0000-0002-1060-5244
Adeline DehlingerExperimental and Clinical Research Center, a cooperation between the Max Delbrück Center for Molecular Medicine in the Helmholtz Association and Charité Universitätsmedizin Berlin, Berlin, 13125, Germany.ORCID 0000-0001-6611-114X
Claudia DamesDepartment of Neurology and Experimental Neurology, Charité-Universitätsmedizin Berlin, Berlin, 10117, Germany.ORCID 0000-0002-9030-9532
Julia K H LemanDepartment of Neuropsychiatry and Laboratory of Molecular Psychiatry, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, 10117, Germany.
Roland E van DijkDepartment of Translational Neuroscience, University Medical Center Utrecht Brain Center, Utrecht University, 3584 CX, Utrecht, The Netherlands.
Andreas MeiselDepartment of Neurology and Experimental Neurology, Charité-Universitätsmedizin Berlin, Berlin, 10117, Germany.ORCID 0000-0001-7233-5342
Stephan SchlickeiserInstitute of Medical Immunology, BIH Center for Regenerative Therapies (BCRT), Berlin Institute of Health at Charité - Universitätsmedizin Berlin, Berlin, 13353, Germany.ORCID 0000-0003-3142-2890
Desiree KunkelFlow & Mass Cytometry Core Facility, Berlin Institute of Health at Charité - Universitätsmedizin Berlin, Berlin, 13353, Germany.
Elly M HolDepartment of Translational Neuroscience, University Medical Center Utrecht Brain Center, Utrecht University, 3584 CX, Utrecht, The Netherlands.ORCID 0000-0001-5604-2603
Friedemann PaulExperimental and Clinical Research Center, a cooperation between the Max Delbrück Center for Molecular Medicine in the Helmholtz Association and Charité Universitätsmedizin Berlin, Berlin, 13125, Germany.
Maria Kristina ParrInstitute of Pharmacy, Freie Universität Berlin, Berlin, 14195, Germany.ORCID 0000-0001-7407-8300
Josef PrillerDepartment of Neuropsychiatry and Laboratory of Molecular Psychiatry, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, 10117, Germany. josef.priller@charite.de.ORCID 0000-0001-7596-0979
Chotima BöttcherExperimental and Clinical Research Center, a cooperation between the Max Delbrück Center for Molecular Medicine in the Helmholtz Association and Charité Universitätsmedizin Berlin, Berlin, 13125, Germany. chotima.boettcher@charite.de.ORCID 0000-0002-6226-586X
Max Delbrück Center · DEHumboldt-Universität zu Berlin · DEUtrecht University · NLBerlin Institute of Health at Charité - Universitätsmedizin Berlin · DECharité - Universitätsmedizin Berlin · DEFreie Universität Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myeloid cells are suggested as an important player in Alzheimer´s disease (AD). However, its continuum of phenotypic and functional changes across different body compartments and their use as a biomarker in AD remains elusive. Here, we perform multiple state-of-the-art analyses to phenotypically and metabolically characterize immune cells between peripheral blood (n = 117), cerebrospinal fluid (CSF, n = 117), choroid plexus (CP, n = 13) and brain parenchyma (n = 13). We find that CSF cells increase expression of markers involved in inflammation, phagocytosis, and metabolism. Changes in phenotype of myeloid cells from AD patients are more pronounced in CP and brain parenchyma and upon in vitro stimulation, suggesting that AD-myeloid cells are more vulnerable to environmental changes. Our findings underscore the importance of myeloid cells in AD and the detailed characterization across body compartments may serve as a resource for future studies focusing on the assessment of these cells as biomarkers in AD.

Indexed as

Alzheimer DiseaseBiomarkersChoroid PlexusHumansMyeloid CellsMyeloid Progenitor CellsPhenotypeBiomarkers

Identifiers

PMID36418303
PMCPMC9684147
OpenAlexW4309908757

What OpenQuestion holds

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LicenceCC BY
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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.