Evidence map›Paper›PMID 27980033›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

The brain parenchyma has a type I interferon response that can limit virus spread.

Eugene Drokhlyansky, Didem Göz Aytürk, Timothy K Soh, Ryan Chrenek, Elaine O'Loughlin, Charlotte Madore, Oleg Butovsky, Constance L Cepko

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

37 citing papers in PubMed, 54 citations in OpenAlex.

  1. Immune signaling and function in neurodegeneration.The Journal of clinical investigation · 2026
    Review
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  4. Abortive and productive infection of CNS cell types following in vivo delivery of VSV.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  14. Repurposing of Tetracyclines for COVID-19 Neurological and Neuropsychiatric Manifestations: A Valid Option to Control SARS-CoV-2-Associated Neuroinflammation?Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2021
    Article
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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

8 authors at 3 institutions in 1 country.

Eugene DrokhlyanskyDepartment of Genetics, Harvard Medical School, Boston, MA 02115.
Didem Göz AytürkDepartment of Genetics, Harvard Medical School, Boston, MA 02115.
Timothy K SohDepartment of Microbiology and Immunobiology, Program in Virology, Harvard Medical School, Boston, MA 02115.
Ryan ChrenekDepartment of Genetics, Harvard Medical School, Boston, MA 02115.
Elaine O'LoughlinAnn Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115.
Charlotte MadoreAnn Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115.
Oleg ButovskyAnn Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115.
Constance L CepkoDepartment of Genetics, Harvard Medical School, Boston, MA 02115; cepko@genetics.med.harvard.edu.
Harvard University · USHoward Hughes Medical Institute · USBrigham and Women's Hospital · US

Funding

Mouse Neurodevelopmental Behavior CoreU54HD090255 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI POMEROY, SCOTT LOREN · 2016 to 2020
$5.2M
Targeting TGFb/IFNy-IRF8 Signaling to Modulate Monocytes and their Crosstalk with Microglia and Astrocytes to Treat Multiple SclerosisR01NS088137 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI Oleg Butovsky · 2014 to 2026
$4.9M
Development of novel transsynaptic tracers for use in the central nervous systemR01NS083848 · NINDS · HARVARD MEDICAL SCHOOL · PI CEPKO, CONSTANCE L · 2013 to 2017
$1.8M
The role of p97 in protein degradation during aging and diseaseF31AG041582 · NIA · HARVARD MEDICAL SCHOOL · PI DROKHLYANSKY, EUGENE · 2011 to 2013
$92k
NIA NIH HHS F31 AG041582NICHD NIH HHS U54 HD090255NINDS NIH HHS R01 NS083848NINDS NIH HHS R01 NS088137
6 · The paper itself

Abstract

The brain has a tightly regulated environment that protects neurons and limits inflammation, designated "immune privilege." However, there is not an absolute lack of an immune response. We tested the ability of the brain to initiate an innate immune response to a virus, which was directly injected into the brain parenchyma, and to determine whether this response could limit viral spread. We injected vesicular stomatitis virus (VSV), a transsynaptic tracer, or naturally occurring VSV-derived defective interfering particles (DIPs), into the caudate-putamen (CP) and scored for an innate immune response and inhibition of virus spread. We found that the brain parenchyma has a functional type I interferon (IFN) response that can limit VSV spread at both the inoculation site and among synaptically connected neurons. Furthermore, we characterized the response of microglia to VSV infection and found that infected microglia produced type I IFN and uninfected microglia induced an innate immune response following virus injection.

Indexed as

AnimalsBrainImmunity, InnateInterferon Type IMaleMiceMice, Inbred C57BLParenchymal TissueVesicular StomatitisVesiculovirusVirus ReplicationInterferon Type Ibraininnate immunityinterferonvesicular stomatitis virusVSV

Identifiers

PMID27980033
PMCPMC5224383
OpenAlexW2563106671

What OpenQuestion holds

Textmetadata
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.