Evidence map›Paper›PMID 39744938›Full record

ArticleThe Journal of clinical investigation2025

A single-cell compendium of human cerebrospinal fluid identifies disease-associated immune cell populations.

Claudia Cantoni, Roman A Smirnov, Maria Firulyova, Prabhakar S Andhey, Tara R Bradstreet, Ekaterina Esaulova, Marina Terekhova, Elizabeth A Schwarzkopf, Nada M Abdalla, Maksim Kleverov and 8 more

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2025. 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
–field-weighted citation impact
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.

  1. Review
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  3. CD8Nature communications · 2026
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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

18 authors.

Claudia CantoniDepartment of Translational Neuroscience, Barrow Neurological Institute, Phoenix, Arizona USA.
Roman A SmirnovDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Maria FirulyovaDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Prabhakar S AndheyDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Tara R BradstreetDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Ekaterina EsaulovaDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Marina TerekhovaDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Elizabeth A SchwarzkopfDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Nada M AbdallaDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Maksim KleverovDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Joseph J SabatinoWeill Institute for Neurosciences, UCSF, San Francisco, California, USA.
Kang LiuRegeneron Pharmaceuticals, Tarrytown, New York, USA.
Nicholas SchwabDepartment of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany.
Gerd Meyer Zu HörsteDepartment of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany.
Anne H CrossDepartment of Neurology, Washington University School of Medicine, St. Louis, Missouri, USA.
Maxim N ArtyomovDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Brian T EdelsonDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Gregory F WuDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.

Funding

WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
Research Education ComponentP30AG066444 · NIA · WASHINGTON UNIVERSITY · PI Carlos Cruchaga · 2020 to 2026
$28.7M
Detection of disease-relevant CD8+ T cells in Multiple SclerosisK08NS107619 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SABATINO, JOSEPH JOHN · 2019 to 2023
$1.0M
Immunologic Characterization of CSF microglia in multiple sclerosisR21NS121818 · NINDS · WASHINGTON UNIVERSITY · PI EDELSON, BRIAN TODD, WU, GREGORY · 2021 to 2022
$433k
CSRD VA I01 CX002383NCATS NIH HHS UL1 TR002345NIA NIH HHS P30 AG066444NINDS NIH HHS K08 NS107619NINDS NIH HHS R21 NS121818
6 · The paper itself

Abstract

Single-cell transcriptomics applied to cerebrospinal fluid (CSF) for elucidating the pathophysiology of neurologic diseases has produced only a preliminary characterization of CSF immune cells. CSF derives from and borders central nervous system (CNS) tissue, allowing for comprehensive accounting of cell types along with their relative abundance and immunologic profiles relevant to CNS diseases. Using integration techniques applied to publicly available datasets in combination with our own studies, we generated a compendium with 139 subjects encompassing 135 CSF and 58 blood samples. Healthy subjects and individuals across a wide range of diseases, such as multiple sclerosis (MS), Alzheimer's disease, Parkinson's disease, COVID-19, and autoimmune encephalitis, were included. We found differences in lymphocyte and myeloid subset frequencies across different diseases as well as in their distribution between blood and CSF. We identified what we believe to be a new subset of AREG+ dendritic cells exclusive to the CSF that was more abundant in subjects with MS compared with healthy controls. Finally, transcriptional cell states in CSF microglia-like cells and lymphoid subsets were elucidated. Altogether, we have created a reference compendium for single-cell transcriptional profiling encompassing CSF immune cells useful to the scientific community for future studies on neurologic diseases.

Indexed as

COVID-19Multiple SclerosisSingle-Cell AnalysisAdultAgedAlzheimer DiseaseDendritic CellsFemaleHumansMaleMicrogliaMiddle AgedParkinson DiseaseSARS-CoV-2TranscriptomeAdaptive immunityImmunologyInnate immunityNeurological disordersNeuroscience

Identifiers

PMID39744938
PMCPMC11684814

What OpenQuestion holds

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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.