| Literature DB >> 30232286 |
Shelli F Farhadian1,2, Sameet S Mehta3, Chrysoula Zografou2,4, Kevin Robertson5, Richard W Price6, Jenna Pappalardo3,4, Jennifer Chiarella2, David A Hafler2,4, Serena S Spudich2.
Abstract
Central nervous system (CNS) immune activation is an important driver of neuronal injury during several neurodegenerative and neuroinflammatory diseases. During HIV infection, CNS immune activation is associated with high rates of neurocognitive impairment, even during sustained long-term suppressive antiretroviral therapy (ART). However, the cellular subsets that drive immune activation and neuronal damage in the CNS during HIV infection and other neurological conditions remain unknown, in part because CNS cells are difficult to access in living humans. Using single-cell RNA sequencing (scRNA-seq) on cerebrospinal fluid (CSF) and blood from adults with and without HIV, we identified a rare (<5% of cells) subset of myeloid cells that are found only in CSF and that present a gene expression signature that overlaps significantly with neurodegenerative disease-associated microglia. This highlights the power of scRNA-seq of CSF to identify rare CNS immune cell subsets that may perpetuate neuronal injury during HIV infection and other conditions.Entities:
Keywords: AIDS/HIV; Inflammation; Neurological disorders
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Year: 2018 PMID: 30232286 PMCID: PMC6237230 DOI: 10.1172/jci.insight.121718
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708