Evidence map›Paper›PMID 25270030›Full record

ReviewThe Journal of pathology2015

Molecular pathology of emerging coronavirus infections.

Lisa E Gralinski, Ralph S Baric

Registry-linked trialAbstract readReview
In one paragraph

Review in The Journal of pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04393246 (mulTi-Arm Therapeutic Study in Pre-ICu Patients Admitted With Covid-19 - Experimental Drugs and Mechanisms), which is not on this map. Cited by 199 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
199citing papers in PubMed, 7 pooled it
–field-weighted citation impact
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.

NCT04393246 phase2 / phase3completednot on this mapstarted 2020, after this paper: background citation

mulTi-Arm Therapeutic Study in Pre-ICu Patients Admitted With Covid-19 - Experimental Drugs and Mechanisms (TACTIC-E)

TypeinterventionalSponsorCambridge University Hospitals NHS Foundation TrustRan2020 to 2022Enrolled454ConditionsCOVID-19ArmsEDP1815, Dapagliflozin, Ambrisentan, Standard of care
3 · Its place in the literature

Who cites it

199 citing papers in PubMed, 7 syntheses or guidelines pooled it.

  1. Genetic polymorphisms as multi-biomarkers in severe acute respiratory syndrome (SARS) by coronavirus infection: A systematic review of candidate gene association studies.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2021
    Pooled it
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  4. A systematic review of pathological findings in COVID-19: a pathophysiological timeline and possible mechanisms of disease progression.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2020
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139 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

2 authors.

Lisa E GralinskiDepartment of Epidemiology, University of North Carolina, Chapel Hill, NC, USA.
Ralph S Baric

Funding

Unlocking Zika Virus Immune Control and Pathogenesis with the Collaborative CrossU19AI100625 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HEISE, MARK T · 2012 to 2021
$36.6M
Translational CoreU19AI109761 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI BARIC, RALPH S · 2014 to 2018
$32.6M
NIAID NIH HHS HHSN272200800060CNIAID NIH HHS U19 AI100625NIAID NIH HHS U19 AI109761NIAID NIH HHS U19AI109761
6 · The paper itself

Abstract

Respiratory viruses can cause a wide spectrum of pulmonary diseases, ranging from mild, upper respiratory tract infections to severe and life-threatening lower respiratory tract infections, including the development of acute lung injury (ALI) and acute respiratory distress syndrome (ARDS). Viral clearance and subsequent recovery from infection require activation of an effective host immune response; however, many immune effector cells may also cause injury to host tissues. Severe acute respiratory syndrome (SARS) coronavirus and Middle East respiratory syndrome (MERS) coronavirus cause severe infection of the lower respiratory tract, with 10% and 35% overall mortality rates, respectively; however, >50% mortality rates are seen in the aged and immunosuppressed populations. While these viruses are susceptible to interferon treatment in vitro, they both encode numerous genes that allow for successful evasion of the host immune system until after high virus titres have been achieved. In this review, we discuss the importance of the innate immune response and the development of lung pathology following human coronavirus infection.

Indexed as

Communicable Diseases, EmergingAnimalsAntiviral AgentsBiopsyCoronavirusCoronavirus InfectionsHost-Pathogen InteractionsHumansImmunity, InnateMiddle East Respiratory Syndrome CoronavirusPathology, MolecularPredictive Value of TestsRespiratory SystemRisk FactorsSevere Acute Respiratory SyndromeSevere acute respiratory syndrome-related coronavirusAntiviral Agentsacute lung injuryacute respiratory distress syndromeARDScoronavirusMERS-CoVSARS-CoVtype II pneumocytes

Identifiers

PMID25270030
PMCPMC4267971

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.