Evidence map›Paper›PMID 28077630›Full record

ArticleJournal of virology2017

MAVS Is Essential for Primary CD4

Huanle Luo, Evandro Winkelmann, Guorui Xie, Rong Fang, Bi-Hung Peng, Li Li, Helen M Lazear, Slobodan Paessler, Michael S Diamond, Michael Gale and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

10 citing papers in PubMed, 12 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

12 authors at 4 institutions in 1 country.

Huanle LuoDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, USA.
Evandro WinkelmannDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, USA.
Guorui XieDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, USA.
Rong FangDepartment of Pathology, University of Texas Medical Branch, Galveston, Texas, USA.
Bi-Hung PengDepartment of Neuroscience and Cell Biology, University of Texas Medical Branch, Galveston, Texas, USA.
Li LiDepartment of Pathology, University of Texas Medical Branch, Galveston, Texas, USA.
Helen M LazearDepartment of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Slobodan PaesslerDepartment of Pathology, University of Texas Medical Branch, Galveston, Texas, USA.
Michael S DiamondDepartment of Medicine, Washington University, St. Louis, Missouri, USA.
Michael GaleDepartment of Immunology, University of Washington School of Medicine, Seattle, Washington, USA.
Alan D BarrettDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, USA.
Tian WangDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, USA ti1wang@utmb.edu.
The University of Texas Medical Branch at Galveston · USUniversity of North Carolina at Chapel Hill · USUniversity of Washington · USWashington University in St. Louis · US

Funding

West Nile Virus and host control of innate defensesU19AI083019 · NIAID · UNIVERSITY OF WASHINGTON · PI CLARK, EDWARD A · 2009 to 2018
$22.5M
Innate Immune Control of West Nile VirusR01AI104002 · NIAID · UNIVERSITY OF WASHINGTON · PI DIAMOND, MICHAEL S, GALE, MICHAEL · 2013 to 2017
$3.7M
Rational Development of Candidate Attenuated Flavivirus VaccinesR01AI099123 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI WANG, TIAN · 2013 to 2016
$1.8M
Cell-Specific Programs of Host Defense Against West Nile VirusR01AI074973 · NIAID · UNIVERSITY OF WASHINGTON · PI GALE, MICHAEL · 2009 to 2010
$774k
NIAID NIH HHS R01 AI074973NIAID NIH HHS R01 AI099123NIAID NIH HHS R01 AI104002NIAID NIH HHS U19 AI083019
6 · The paper itself

Abstract

The use of pathogen recognition receptor (PRR) agonists and the molecular mechanisms involved have been the major focus of research in individual vaccine development. West Nile virus (WNV) nonstructural (NS) 4B-P38G mutant has several features for an ideal vaccine candidate, including significantly reduced neuroinvasiveness, induction of strong adaptive immunity, and protection of mice from wild-type (WT) WNV infection. Here, we determined the role of mitochondrial antiviral signaling protein (MAVS), the adaptor protein for RIG-I-like receptor in regulating host immunity against the NS4B-P38G vaccine. We found that

Indexed as

Adaptive ImmunityImmunity, InnateAdaptor Proteins, Signal TransducingAnimalsAntibodies, ViralCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesDendritic CellsMiceMice, KnockoutWest Nile virusWest Nile Virus VaccinesAdaptor Proteins, Signal TransducingAntibodies, ViralMAVS protein, mouseWest Nile Virus Vaccinesadaptive immunityMAVST cellT cellsvaccineWest Nile virus

Identifiers

PMID28077630
PMCPMC5331791
OpenAlexW2578052194

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.