Evidence map›Paper›PMID 25122141›Full record

ArticlePLoS pathogens2014

Inhibition of the TRAIL death receptor by CMV reveals its importance in NK cell-mediated antiviral defense.

Shilpi Verma, Andrea Loewendorf, Qiao Wang, Bryan McDonald, Alec Redwood, Chris A Benedict

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.9field-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

23 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  8. HCMV-secreted glycoprotein gpUL4 inhibits TRAIL-mediated apoptosis and NK cell activation.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
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  15. Cytomegalovirus: Shape-Shifting the Immune System.Journal of immunology (Baltimore, Md. : 1950) · 2018
    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

6 authors at 2 institutions in 2 countries.

Shilpi VermaDivision of Immune Regulation, La Jolla Institute for Allergy and Immunology, La Jolla, California, United States of America.
Andrea LoewendorfDivision of Immune Regulation, La Jolla Institute for Allergy and Immunology, La Jolla, California, United States of America.
Qiao WangDivision of Immune Regulation, La Jolla Institute for Allergy and Immunology, La Jolla, California, United States of America.
Bryan McDonaldDivision of Immune Regulation, La Jolla Institute for Allergy and Immunology, La Jolla, California, United States of America.
Alec RedwoodMicrobiology and Immunology, School of Pathology and Laboratory Medicine, University of Western Australia, Crawley, Western Australia, Australia.
Chris A BenedictDivision of Immune Regulation, La Jolla Institute for Allergy and Immunology, La Jolla, California, United States of America.
La Jolla Institute for Immunology · USUniversity of Western Australia · AU

Funding

The role of TRAIL in immune control of cytomegalovirusR01AI101423 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI BENEDICT, CHRISTOPHER A · 2013 to 2023
$4.6M
Activation of NKT cells by cytomegalovirusR21AI076864 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI BENEDICT, CHRISTOPHER A, KRONENBERG, MITCHELL · 2009 to 2010
$519k
The role of TRAIL in immune control of cytomegalovirusR56AI101423 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI BENEDICT, CHRISTOPHER A · 2012 to 2012
$435k
NIAID NIH HHS AI076864NIAID NIH HHS AI101423NIAID NIH HHS R01 AI101423NIAID NIH HHS R21 AI076864NIAID NIH HHS R56 AI101423
6 · The paper itself

Abstract

TNF-related apoptosis inducing ligand (TRAIL) death receptors (DR) regulate apoptosis and inflammation, but their role in antiviral defense is poorly understood. Cytomegaloviruses (CMV) encode many immune-modulatory genes that shape host immunity, and they utilize multiple strategies to target the TNF-family cytokines. Here we show that the m166 open reading frame (orf) of mouse CMV (MCMV) is strictly required to inhibit expression of TRAIL-DR in infected cells. An MCMV mutant lacking m166 expression (m166stop) is severely compromised for replication in vivo, most notably in the liver, and depleting natural killer (NK) cells, or infecting TRAIL-DR-/- mice, restored MCMV-m166stop replication completely. These results highlight the critical importance for CMV to have evolved a strategy to inhibit TRAIL-DR signaling to thwart NK-mediated defenses.

Indexed as

AnimalsBlotting, WesternCytomegalovirus InfectionsDisease Models, AnimalFlow CytometryFluorescent Antibody TechniqueKiller Cells, NaturalMiceMice, Inbred BALB CMice, Inbred C57BLMice, KnockoutMuromegalovirusNIH 3T3 CellsReceptors, TNF-Related Apoptosis-Inducing LigandReverse Transcriptase Polymerase Chain ReactionViral ProteinsReceptors, TNF-Related Apoptosis-Inducing LigandViral Proteins

Identifiers

PMID25122141
PMCPMC4133390
OpenAlexW1964575951

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.