Evidence map›Paper›PMID 33544398›Full record

ArticleEMBO molecular medicine2021

Epithelial response to IFN-γ promotes SARS-CoV-2 infection.

Julian Heuberger, Jakob Trimpert, Daria Vladimirova, Christian Goosmann, Manqiang Lin, Rosa Schmuck, Hans-Joachim Mollenkopf, Volker Brinkmann, Frank Tacke, Nikolaus Osterrieder and 1 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
5.3field-weighted citation impact, top 3% 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

55 citing papers in PubMed, 88 citations in OpenAlex.

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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

11 authors at 5 institutions in 3 countries.

Julian HeubergerDepartment of Hepatology and Gastroenterology, Charité University Medicine, Berlin, Germany.
Jakob TrimpertInstitute of Virology, Freie Universität Berlin, Berlin, Germany.
Daria VladimirovaInstitute of Virology, Freie Universität Berlin, Berlin, Germany.
Christian GoosmannDepartment of Molecular Biology, Max Planck Institute for Infection Biology, Berlin, Germany.
Manqiang LinDepartment of Hepatology and Gastroenterology, Charité University Medicine, Berlin, Germany.
Rosa SchmuckDepartment of Surgery, Charité University Medicine, Berlin, Germany.
Hans-Joachim MollenkopfDepartment of Molecular Biology, Max Planck Institute for Infection Biology, Berlin, Germany.
Volker BrinkmannDepartment of Molecular Biology, Max Planck Institute for Infection Biology, Berlin, Germany.
Frank TackeDepartment of Hepatology and Gastroenterology, Charité University Medicine, Berlin, Germany.
Nikolaus OsterriederInstitute of Virology, Freie Universität Berlin, Berlin, Germany.
Michael SigalDepartment of Hepatology and Gastroenterology, Charité University Medicine, Berlin, Germany.ORCID 0000-0003-4772-0761
Charité - Universitätsmedizin Berlin · DEMax Planck Institute for Infection Biology · DEFreie Universität Berlin · DEMax Delbrück Center · DECity University of Hong Kong · HK

Funding

DFG Si-1983/3-1DFG Si-1983/4-1
6 · The paper itself

Abstract

SARS-CoV-2, the agent that causes COVID-19, invades epithelial cells, including those of the respiratory and gastrointestinal mucosa, using angiotensin-converting enzyme-2 (ACE2) as a receptor. Subsequent inflammation can promote rapid virus clearance, but severe cases of COVID-19 are characterized by an inefficient immune response that fails to clear the infection. Using primary epithelial organoids from human colon, we explored how the central antiviral mediator IFN-γ, which is elevated in COVID-19, affects epithelial cell differentiation, ACE2 expression, and susceptibility to infection with SARS-CoV-2. In mouse and human colon, ACE2 is mainly expressed by surface enterocytes. Inducing enterocyte differentiation in organoid culture resulted in increased ACE2 production. IFN-γ treatment promoted differentiation into mature KRT20

Indexed as

Models, ImmunologicalSARS-CoV-2Angiotensin-Converting Enzyme 2AnimalsCell DifferentiationColonCOVID-19Disease SusceptibilityEnterocytesGene ExpressionHost Microbial InteractionsHumansInterferon-gammaIntestinal MucosaMiceOrganoidsACE2 protein, humanAce2 protein, mouseAngiotensin-Converting Enzyme 2Interferon-gammaACE2differentiationinterferonorganoidsSARS-CoV-2

Identifiers

PMID33544398
PMCPMC7995094
OpenAlexW3127706820

What Socratic 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 Socratic graph.