Evidence map›Paper›PMID 24198408›Full record

ArticleJournal of virology2014

Inhibition of NF-κB-mediated inflammation in severe acute respiratory syndrome coronavirus-infected mice increases survival.

Marta L DeDiego, Jose L Nieto-Torres, Jose A Regla-Nava, Jose M Jimenez-Guardeño, Raul Fernandez-Delgado, Craig Fett, Carlos Castaño-Rodriguez, Stanley Perlman, Luis Enjuanes

2 registry-linked trialsOpen access · greenAbstract read
In one paragraph

Article in Journal of virology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 287 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
287citing papers in PubMed, 4 pooled it
4.7field-weighted citation impact, top 4% 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.

NCT04368156 nacompletednot on this mapstarted 2020, after this paper: background citation

A Prospective, Randomized, Controlled Study Assessing Vagus Nerve Stimulation in CoViD-19 Respiratory Symptoms (SAVIOR)

TypeinterventionalSponsorCarlos TorneroRan2020 to 2021Enrolled110ConditionsCovid-19ArmsgammaCore® (Vagus nerve stimulation)
NCT04894617 phase3unknown statusnot on this mapstarted 2021, after this paper: background citation

Amantadine for COVID-19: A Randomized, Placebo Controlled, Double-blinded, Clinical Trial

TypeinterventionalSponsorCopenhagen University Hospital, HvidovreRan2021 to 2022Enrolled226ConditionsCovid19ArmsAmantadine, Lactose monohydrate
3 · Its place in the literature

Who cites it

287 citing papers in PubMed, 4 syntheses or guidelines pooled it, 418 citations in OpenAlex.

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  19. Regulatory role of microRNAs in virus-mediated inflammation.Journal of inflammation (London, England) · 2024
    Review
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227 more citing papers are in PubMed but not listed here.

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

9 authors at 2 institutions in 2 countries.

Marta L DeDiegoDepartment of Molecular and Cell Biology, National Center of Biotechnology, Campus Universidad Autónoma de Madrid, Madrid, Spain.
Jose L Nieto-Torres
Jose A Regla-Nava
Jose M Jimenez-Guardeño
Raul Fernandez-Delgado
Craig Fett
Carlos Castaño-Rodriguez
Stanley Perlman
Luis Enjuanes
Universidad Autónoma de Madrid · ESUniversity of Iowa · US

Funding

SARS-CoV Proteins in Heterologous Viral InfectionP01AI060699 · NIAID · UNIVERSITY OF IOWA · PI PERLMAN, STANLEY · 2004 to 2021
$21.5M
NIAID NIH HHS 2P01AI060699-06A1NIAID NIH HHS HHSN266200700010CNIAID NIH HHS P01 AI060699
6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus (SARS-CoV) is the etiological agent of a respiratory disease that has a 10% mortality rate. We previously showed that SARS-CoV lacking the E gene (SARS-CoV-ΔE) is attenuated in several animal model systems. Here, we show that absence of the E protein resulted in reduced expression of proinflammatory cytokines, decreased numbers of neutrophils in lung infiltrates, diminished lung pathology, and increased mouse survival, suggesting that lung inflammation contributed to SARS-CoV virulence. Further, infection with SARS-CoV-ΔE resulted in decreased activation of NF-κB compared to levels for the wild-type virus. Most important, treatment with drugs that inhibited NF-κB activation led to a reduction in inflammation and lung pathology in both SARS-CoV-infected cultured cells and mice and significantly increased mouse survival after SARS-CoV infection. These data indicated that activation of the NF-κB signaling pathway represents a major contribution to the inflammation induced after SARS-CoV infection and that NF-κB inhibitors are promising antivirals in infections caused by SARS-CoV and potentially other pathogenic human coronaviruses.

Indexed as

Down-RegulationAnimalsCytokinesFemaleHumansMiceMice, Inbred BALB CNF-kappa BSevere Acute Respiratory SyndromeSevere acute respiratory syndrome-related coronavirusViral Envelope ProteinsViroporin ProteinsCytokinesE protein, SARS coronavirusNF-kappa BViral Envelope ProteinsViroporin Proteins

Identifiers

PMID24198408
PMCPMC3911641
OpenAlexW2061786382

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.