Evidence map›Paper›PMID 27466418›Full record

ArticleJournal of virology2016

Abelson Kinase Inhibitors Are Potent Inhibitors of Severe Acute Respiratory Syndrome Coronavirus and Middle East Respiratory Syndrome Coronavirus Fusion.

Christopher M Coleman, Jeanne M Sisk, Rebecca M Mingo, Elizabeth A Nelson, Judith M White, Matthew B Frieman

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Journal of virology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04794088 (A Randomised, Double-blind, Placebo-controlled Study to Investigate the Safety and Efficacy of Intravenous Imatinib Mesylate), which is not on this map. Cited by 156 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
156citing papers in PubMed, 7 pooled it
3.2field-weighted citation impact, top 8% 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.

NCT04794088 phase2terminatednot on this mapstarted 2021, after this paper: background citation

A Randomised, Double-blind, Placebo-controlled Study to Investigate the Safety and Efficacy of Intravenous Imatinib Mesylate (Impentri®) in Subjects With Acute Respiratory Distress Syndrome Induced by COVID-19

TypeinterventionalSponsorDr. Jurjan AmanRan2021 to 2022Enrolled67ConditionsARDS, Acute Respiratory Distress Syndrome, Covid19, Endothelial DysfunctionArmsImatinib Mesylate intravenous solution, Placebo
3 · Its place in the literature

Who cites it

156 citing papers in PubMed, 7 syntheses or guidelines pooled it, 274 citations in OpenAlex.

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  11. Design, Synthesis and Biological Exploration of NovelInternational journal of molecular sciences · 2024
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96 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

6 authors at 2 institutions in 1 country.

Christopher M ColemanDepartment of Microbiology and Immunology, University of Maryland, Baltimore, Maryland, USA.
Jeanne M SiskDepartment of Microbiology and Immunology, University of Maryland, Baltimore, Maryland, USA.
Rebecca M MingoDepartment of Cell Biology, University of Virginia, Charlottesville, Virginia, USA.
Elizabeth A NelsonDepartment of Cell Biology, University of Virginia, Charlottesville, Virginia, USA.
Judith M WhiteDepartment of Cell Biology, University of Virginia, Charlottesville, Virginia, USA.
Matthew B FriemanDepartment of Microbiology and Immunology, University of Maryland, Baltimore, Maryland, USA mfrieman@som.umaryland.edu.
University of Maryland, Baltimore · USUniversity of Virginia · US

Funding

Role of the Epithelial Growth Factor Receptor in SARS Coronavirus PathogenesisR01AI095569 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI FRIEMAN, MATTHEW BRYAN · 2011 to 2016
$2.3M
Combinations of Approved Drugs to Combat Ebola VirusR01AI114776 · NIAID · UNIVERSITY OF VIRGINIA · PI WHITE, JUDITH M. · 2015 to 2017
$1.5M
A Novel Viral Membrane Fusion Triggering MechanismR21AI103601 · NIAID · UNIVERSITY OF VIRGINIA · PI WHITE, JUDITH M. · 2013 to 2014
$420k
Repurposing of ABL kinase inhibitors for treatment of Coronavirus infectionsF32AI118303 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI SISK, JEANNE · 2015 to 2017
$167k
NIAID NIH HHS F32 AI118303NIAID NIH HHS R01 AI095569NIAID NIH HHS R01 AI114776NIAID NIH HHS R21 AI103601
6 · The paper itself

Abstract

unlabelledThe highly pathogenic severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome coronavirus (MERS-CoV) cause significant morbidity and morality. There is currently no approved therapeutic for highly pathogenic coronaviruses, even as MERS-CoV is spreading throughout the Middle East. We previously screened a library of FDA-approved drugs for inhibitors of coronavirus replication in which we identified Abelson (Abl) kinase inhibitors, including the anticancer drug imatinib, as inhibitors of both SARS-CoV and MERS-CoV in vitro Here we show that the anti-CoV activity of imatinib occurs at the early stages of infection, after internalization and endosomal trafficking, by inhibiting fusion of the virions at the endosomal membrane. We specifically identified the imatinib target, Abelson tyrosine-protein kinase 2 (Abl2), as required for efficient SARS-CoV and MERS-CoV replication in vitro These data demonstrate that specific approved drugs can be characterized in vitro for their anticoronavirus activity and used to identify host proteins required for coronavirus replication. This type of study is an important step in the repurposing of approved drugs for treatment of emerging coronaviruses. IMPORTANCE: Both SARS-CoV and MERS-CoV are zoonotic infections, with bats as the primary source. The 2003 SARS-CoV outbreak began in Guangdong Province in China and spread to humans via civet cats and raccoon dogs in the wet markets before spreading to 37 countries. The virus caused 8,096 confirmed cases of SARS and 774 deaths (a case fatality rate of ∼10%). The MERS-CoV outbreak began in Saudi Arabia and has spread to 27 countries. MERS-CoV is believed to have emerged from bats and passed into humans via camels. The ongoing outbreak of MERS-CoV has resulted in 1,791 cases of MERS and 640 deaths (a case fatality rate of 36%). The emergence of SARS-CoV and MERS-CoV provides evidence that coronaviruses are currently spreading from zoonotic sources and can be highly pathogenic, causing serious morbidity and mortality in humans. Treatment of SARS-CoV and MERS-CoV infection is limited to providing supportive therapy consistent with any serious lung disease, as no specific drugs have been approved as therapeutics. Highly pathogenic coronaviruses are rare and appear to emerge and disappear within just a few years. Currently, MERS-CoV is still spreading, as new infections continue to be reported. The outbreaks of SARS-CoV and MERS-CoV and the continuing diagnosis of new MERS cases highlight the need for finding therapeutics for these diseases and potential future coronavirus outbreaks. Screening FDA-approved drugs streamlines the pipeline for this process, as these drugs have already been tested for safety in humans.

Indexed as

AnimalsAntiviral AgentsCell LineHumansImatinib MesylateMiddle East Respiratory Syndrome CoronavirusProtein Kinase InhibitorsProtein-Tyrosine KinasesSevere acute respiratory syndrome-related coronavirusVirus InternalizationAntiviral AgentsARG tyrosine kinaseImatinib MesylateProtein Kinase InhibitorsProtein-Tyrosine Kinases

Identifiers

PMID27466418
PMCPMC5021412
OpenAlexW2520543291

What OpenQuestion holds

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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.