Evidence map›Paper›PMID 25777301›Full record

ArticleMicrobes and infection2015

IRF3 deficiency impacts granzyme B expression and maintenance of memory T cell function in response to viral infection.

Tyler C Moore, Alexander J Vogel, Thomas M Petro, Deborah M Brown

Open access · greenAbstract read
In one paragraph

Article in Microbes and infection, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

13 citing papers in PubMed, 15 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

Tyler C MooreSchool of Biological Sciences, University of Nebraska-Lincoln, USA.
Alexander J VogelSchool of Biological Sciences, University of Nebraska-Lincoln, USA.
Thomas M PetroNebraska Center for Virology, University of Nebraska-Lincoln, USA; Department of Oral Biology, University of Nebraska Medical Center, USA.
Deborah M BrownSchool of Biological Sciences, University of Nebraska-Lincoln, USA; Nebraska Center for Virology, University of Nebraska-Lincoln, USA. Electronic address: dbrown7@unl.edu.
University of Nebraska–Lincoln · US

Funding

SUPPRESSIVE ROLE OF TGFBETA IN METASTASIS OF COLON CANCERP20RR018759 · NCRR · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI WAHL, JAMES K · 2003 to 2011
$17.9M
Research Pilot Project ProgramP30GM106397 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI JOHNSON, KEITH R · 2013 to 2017
$4.9M
Nebraska Center for VirologyP30GM103509 · NIGMS · UNIVERSITY OF NEBRASKA LINCOLN · PI WOOD, CHARLES · 2012 to 2014
$3.3M
Research Training in Comparative Viral PathogenesisT32AI060547 · NIAID · UNIVERSITY OF NEBRASKA LINCOLN · PI WOOD, CHARLES · 2004 to 2013
$2.5M
Nebraska Center for Cellular SignalingP20GM103489 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI JOHNSON, KEITH R · 2012 to 2012
$2.0M
Generation and Regulation of Anti-Viral CD4 T Cells with Cytolytic PotentialR56AI100929 · NIAID · UNIVERSITY OF NEBRASKA LINCOLN · PI BROWN, DEBORAH M. · 2013 to 2013
$351k
NCRR NIH HHS P20 RR018759NCRR NIH HHS P20-RR018759NIAID NIH HHS R56 AI100929NIAID NIH HHS R56-AI100929NIAID NIH HHS T32 AI060547NIAID NIH HHS T32-AI060547NIGMS NIH HHS P20 GM103489NIGMS NIH HHS P30 GM103509NIGMS NIH HHS P30-GM103509NIGMS NIH HHS P30 GM106397
6 · The paper itself

Abstract

The role of interferon regulatory factor 3 (IRF3) in the innate immune response to infection has been well studied. However, less is known about IRF3 signaling in shaping the adaptive T cell response. To determine the role of IRF3 in the generation and maintenance of effective anti-viral T cell responses, mice deficient in IRF3 were infected with a potentially persistent virus, Theiler's murine encephalomyelitis virus (TMEV) or with a model acute infection, influenza A virus (IAV). IRF3 was required to prevent TMEV persistence and induce robust TMEV specific effector T cell responses at the site of infection. This defect was more pronounced in the memory phase with an apparent lack of TMEV-specific memory T cells expressing granzyme B (GrB) in IRF3 deficient mice. In contrast, IRF3 had no effect on antigen specific T cell responses at the effector stage during IAV infection. However, memory T cell responses to IAV were also impaired in IRF3 deficient mice. Furthermore, addition of cytokines during peptide restimulation could not restore GrB expression in IRF3 deficient memory T cells. Taken together, IRF3 plays an important role in the maintenance of effective anti-viral T cell memory responses.

Indexed as

AnimalsGranzymesInterferon Regulatory Factor-3MiceSignal TransductionTheilovirusT-LymphocytesGranzymesInterferon Regulatory Factor-3IRF3 protein, humanCytokinesInfluenza A virusInterferon regulatory factor-3T cell memoryT cellsTheiler's murine encephalomyelitis virus

Identifiers

PMID25777301
PMCPMC4479197
OpenAlexW2067025384

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.