Evidence map›Paper›PMID 35366686›Full record

ReviewMedical microbiology and immunology2023

Interferon antagonists encoded by SARS-CoV-2 at a glance.

Jung-Hyun Lee, Lennart Koepke, Frank Kirchhoff, Konstantin M J Sparrer

Open access · hybridAbstract readReview
In one paragraph

Review in Medical microbiology and immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

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  18. The role of SARS-CoV-2 accessory proteins in immune evasion.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2022
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

Jung-Hyun Lee *Institute of Molecular Virology, Ulm University Medical Center, Meyerhofstr. 1, 89081, Ulm, Germany.ORCID http://orcid.org/0000-0003-1913-0027
Lennart Koepke *Institute of Molecular Virology, Ulm University Medical Center, Meyerhofstr. 1, 89081, Ulm, Germany.ORCID http://orcid.org/0000-0001-9788-1972
Frank KirchhoffInstitute of Molecular Virology, Ulm University Medical Center, Meyerhofstr. 1, 89081, Ulm, Germany.
Konstantin M J SparrerInstitute of Molecular Virology, Ulm University Medical Center, Meyerhofstr. 1, 89081, Ulm, Germany. Konstantin.Sparrer@uni-ulm.de.ORCID http://orcid.org/0000-0002-8682-1779
Universität Ulm · DEUniversity of Seoul · KR

Funding

Bundesministerium für Bildung und Forschung IMMUNOMODBundesministerium für Bildung und Forschung Restrict SARS-CoV-2Deutsche Forschungsgemeinschaft 1600/6-1Deutsche Forschungsgemeinschaft CRC1279Deutsche Forschungsgemeinschaft SPP1923
6 · The paper itself

Abstract

The innate immune system is a powerful barrier against invading pathogens. Interferons (IFNs) are a major part of the cytokine-mediated anti-viral innate immune response. After recognition of a pathogen by immune sensors, signaling cascades are activated that culminate in the release of IFNs. These activate cells in an autocrine or paracrine fashion eventually setting cells in an anti-viral state via upregulation of hundreds of interferon-stimulated genes (ISGs). To evade the anti-viral effect of the IFN system, successful viruses like the pandemic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) evolved strategies to counteract both IFN induction and signaling. In fact, more than half of the about 30 proteins encoded by SARS-CoV-2 target the IFN system at multiple levels to escape IFN-mediated restriction. Here, we review recent insights into the molecular mechanisms used by SARS-CoV-2 proteins to suppress IFN production and the establishment of an anti-viral state.

Indexed as

COVID-19InterferonsAntiviral AgentsHumansImmunity, InnateSARS-CoV-2Antiviral AgentsInterferonsCOVID-19Immune evasionInnate immunityInterferonSARS-CoV-2

Identifiers

PMID35366686
PMCPMC8976456
OpenAlexW4226207319

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.