Evidence map›Paper›PMID 25669994›Full record

ArticleJournal of neuroimmunology2015

Homeostatic interferon expression in neurons is sufficient for early control of viral infection.

Sarah E Cavanaugh, Alicia M Holmgren, Glenn F Rall

Abstract read
In one paragraph

Article in Journal of neuroimmunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

26 citing papers in PubMed, 35 citations in OpenAlex.

  1. Getting on your last nerve: IFNs and resistance to infection.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Review
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  17. Human iPSC-Derived Neuronal Cells FromFrontiers in neuroscience · 2020
    Article
  18. Review
  19. Article
  20. CNS infection and immune privilege.Nature reviews. Neuroscience · 2018
    Review
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

3 authors at 2 institutions in 1 country.

Sarah E CavanaughFox Chase Cancer Center, Program in Immune Cell Development and Host Defense, 333 Cottman Avenue, Philadelphia, PA 19111, United States; Department of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA 19129, United States.
Alicia M HolmgrenFox Chase Cancer Center, Program in Immune Cell Development and Host Defense, 333 Cottman Avenue, Philadelphia, PA 19111, United States; Department of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA 19129, United States.
Glenn F RallFox Chase Cancer Center, Program in Immune Cell Development and Host Defense, 333 Cottman Avenue, Philadelphia, PA 19111, United States. Electronic address: glenn.rall@fccc.edu.
Drexel University · USFox Chase Cancer Center · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Margaret von Mehren · 1985 to 2026
$138.8M
Intra- and Inter-Neuronal Viral TraffickingR01NS060701 · NINDS · RESEARCH INST OF FOX CHASE CAN CTR · PI RALL, GLENN F · 2008 to 2012
$2.1M
Pathogenesis of Neurotropic RNA Virus InfectionsR01NS040500 · NINDS · RESEARCH INST OF FOX CHASE CAN CTR · PI RALL, GLENN F · 2002 to 2006
$1.6M
Analysis of neuronal signaling pathways following interferon stimulationF31NS076202 · NINDS · DREXEL UNIVERSITY · PI CAVANAUGH, SARAH ELIZABETH · 2011 to 2013
$38k
NCI NIH HHS P30 CA006927NCI NIH HHS P30CA006927NINDS NIH HHS F31 NS076202NINDS NIH HHS NS076202-01A1NINDS NIH HHS R01 NS040500NINDS NIH HHS R01 NS060701NINDS NIH HHS R01 NS40500
6 · The paper itself

Abstract

The mechanisms by which neurons respond to inflammatory mediators such as interferons (IFNs) remain largely undefined. We previously showed that the activation and nuclear localization of the core IFN signaling molecule, Stat1, are muted and delayed in primary mouse hippocampal neurons treated with IFN gamma as compared to control mouse embryonic fibroblasts (MEFs). Here, we show that the kinetics of Stat1 and Stat2 activation following type I IFN exposure are also unique in neurons, affecting gene expression and neuronal response. Specifically, despite lower basal expression of many IFN stimulated genes in neurons, basal expression of the type I IFN themselves is significantly higher in primary hippocampal neurons compared to MEF. Elevated homeostatic IFN in neurons is critical and sufficient for early control of viral infection. These data provide further evidence that neurons exploit unique signaling responses to IFNs, and define an important contribution of homeostatic IFN within the CNS. Such differences are likely critical for the ability of neurons to survive a viral challenge.

Indexed as

2',5'-Oligoadenylate SynthetaseAnimalsCells, CulturedCytokinesDisease Models, AnimalEmbryo, MammalianFibroblastsHippocampusInterferonsMeaslesMeasles virusMembrane Cofactor ProteinMiceMice, TransgenicNeuronsPhosphopyruvate Hydratase2',5'-Oligoadenylate SynthetaseCytokinesG1p2 protein, mouseInterferonsMembrane Cofactor ProteinPhosphopyruvate HydrataseRNA, MessengerSTAT1 Transcription FactorSTAT2 Transcription FactorUbiquitinsInterferonNeuronSignalingStat1Stat2

Identifiers

PMID25669994
PMCPMC4325274
OpenAlexW1978215409

What OpenQuestion holds

Textmetadata
LicenceTDM
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.