Single-cell analysis of cerebrospinal fluid reveals common features of neuroinflammation

Neuroinflammation is often characterized by immune cell infiltrates in the cerebrospinal fluid (CSF). Here, we apply single-cell RNA sequencing to explore the functional characteristics of these cells in patients with various inflammatory, infectious, and non-inflammatory neurological disorders. We show that CSF is distinct from the peripheral blood in terms of both cellular composition and gene expression. We report that the cellular and transcriptional landscape of CSF is altered in neuroinflammation but is strikingly similar across different neuroinflammatory disorders. We find clonal expansion of CSF lymphocytes in all disorders but most pronounced in inflammatory diseases, and we functionally characterize the transcriptional features of these cells. Finally, we explore the genetic control of gene expression in CSF lymphocytes. Our results highlight the common features of immune cells in the CSF compartment across diverse neurological diseases and may help to identify new targets for drug development or repurposing in multiple sclerosis (MS).

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Publication Details

Journal
Cell Reports Medicine
Published
2024-12-20
DOI
https://doi.org/10.1016/j.xcrm.2024.101733
Citations
7
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
1.64

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article

Single-cell analysis of cerebrospinal fluid reveals common features of neuroinflammation

Friederike Held, Benjamin M. Jacobs, Bernhard Hemmer, Raghda Al-Najjar et al.
7 citations
Cell Reports Medicine
Single-cell and spatial transcriptomics
1.64
article

Single-cell analysis of cerebrospinal fluid reveals common features of neuroinflammation

Friederike Held, Benjamin M. Jacobs, Bernhard Hemmer, Raghda Al-Najjar, Maria Ban, Jonathan Else, Christiane Gasperi, Mollie O. McKeon, Albert Pukaj, Sudhakar Reddy Kalluri, S. Sawcer
article en
7 citations

Abstract

Neuroinflammation is often characterized by immune cell infiltrates in the cerebrospinal fluid (CSF). Here, we apply single-cell RNA sequencing to explore the functional characteristics of these cells in patients with various inflammatory, infectious, and non-inflammatory neurological disorders. We show that CSF is distinct from the peripheral blood in terms of both cellular composition and gene expression. We report that the cellular and transcriptional landscape of CSF is altered in neuroinflammation but is strikingly similar across different neuroinflammatory disorders. We find clonal expansion of CSF lymphocytes in all disorders but most pronounced in inflammatory diseases, and we functionally characterize the transcriptional features of these cells. Finally, we explore the genetic control of gene expression in CSF lymphocytes. Our results highlight the common features of immune cells in the CSF compartment across diverse neurological diseases and may help to identify new targets for drug development or repurposing in multiple sclerosis (MS).

Cell Reports MedicineVol. 6(1)
Queen Mary University of London (GB), University of Cambridge (GB), Munich Cluster for Systems Neurology (DE), Technical University of Munich (DE)
National Institute for Health and Care Research, Multiple Sclerosis Society, European Commission, Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, Medical Research Council, NIHR Cambridge Biomedical Research Centre
Zero hunger
Openalex Percentile: Top 16%
Single-cell and spatial transcriptomics
1.64
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