Evidence map›Paper›PMID 40810508›Full record

ArticleJournal of virology2025

Neurovascular pericytes are susceptible to infection by JC polyomavirus.

Bethany A O'Hara, Kaitlin Garabian, Wenqing Yuan, Walter J Atwood, Sheila A Haley

Abstract read
In one paragraph

Article in Journal of virology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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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

5 authors.

Bethany A O'Hara *Department of Cell Biology, Biochemistry, and Molecular Biology, Brown University, Providence, Rhode Island, USA.ORCID 0000-0002-6158-5159
Kaitlin Garabian *Department of Cell Biology, Biochemistry, and Molecular Biology, Brown University, Providence, Rhode Island, USA.ORCID 0009-0002-5385-4889
Wenqing YuanDepartment of Cell Biology, Biochemistry, and Molecular Biology, Brown University, Providence, Rhode Island, USA.ORCID 0000-0002-8928-4884
Walter J AtwoodDepartment of Cell Biology, Biochemistry, and Molecular Biology, Brown University, Providence, Rhode Island, USA.ORCID 0000-0002-3763-9073
Sheila A HaleyDepartment of Cell Biology, Biochemistry, and Molecular Biology, Brown University, Providence, Rhode Island, USA.ORCID 0000-0003-2855-5668

Funding

Progressive Multifocal Leukoenephalopathy: Endemic Viruses and Lethal Brain DiseaseR35NS116836 · NINDS · BROWN UNIVERSITY · PI Walter J Atwood · 2020 to 2026
$5.7M
NIH HHS R35 NS5271118NINDS NIH HHS R35 NS116836
6 · The paper itself

Abstract

Progressive multifocal leukoencephalopathy (PML), an often-fatal neurodegenerative disease, is caused by the neuroinvasive polyomavirus JCPyV. Peripheral organs, including the kidney, are the site of lifelong persistent infections that are asymptomatic. In a subset of immunosuppressed or immunomodulated patients, the virus invades the central nervous system infecting oligodendrocytes, which leads to the multifocal white matter disease known as PML. The mechanisms that lead to neuroinvasion by JCPyV have not been well described. The brain is protected from viruses and other pathogens by physiological barriers, including the blood-cerebrospinal fluid barrier and the blood-brain barrier. To better understand the mechanism by which the virus breaches these barriers, we focused our attention on studying virus interactions with pericytes, which are an essential component of the blood-brain barrier. We found that the virus binds to pericytes in a receptor-dependent manner and that pericytes are susceptible to JCPyV infection. Previous work from our group demonstrated that JCPyV was capable of penetrating an intact endothelial cell barrier. Once across the endothelium, JCPyV would come in direct contact with pericytes, and we hypothesize pericyte infection would amplify and facilitate robust penetration into the brain parenchyma. This is the first demonstration that pericytes, a principal component of the blood-brain barrier, are susceptible to the neuroinvasive human polyomavirus JCPyV.IMPORTANCEJCPyV infects at least half the adult population worldwide. An asymptomatic, persistent infection is typically established in the kidney and possibly other peripheral organs. In immunosuppressed individuals, the virus can reactivate and cause progressive multifocal leukoencephalopathy, a deadly disease of the central nervous system (CNS). The pathogenic route the virus takes from the periphery to the CNS is unknown. Here, we demonstrate for the first time that JCPyV can infect human cerebrovascular pericytes, a cell type that contributes to the blood-brain barrier. This observation suggests that the virus could use the pericytes as a means to penetrate the blood-brain barrier to reach its pathogenic targets in the brain parenchyma.

Indexed as

JC VirusPericytesPolyomavirus InfectionsBlood-Brain BarrierBrainCells, CulturedHumansLeukoencephalopathy, Progressive MultifocalPolysaccharidesProtein BindingReceptors, VirusVirus AttachmentVirus InternalizationPolysaccharidesReceptors, Virusblood brain barrierhost rangeJCPyVpericytespolyomavirusprogressive multifocal leukoencephalopathy

Identifiers

PMID40810508
PMCPMC12455973

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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.