Evidence map›Paper›PMID 35334213›Full record

ArticleStem cell reports2022

SARS-CoV-2 infects and replicates in photoreceptor and retinal ganglion cells of human retinal organoids.

Yotam Menuchin-Lasowski, André Schreiber, Aarón Lecanda, Angeles Mecate-Zambrano, Linda Brunotte, Olympia E Psathaki, Stephan Ludwig, Thomas Rauen, Hans R Schöler

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
10.8field-weighted citation impact, top 1% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 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

9 authors at 3 institutions in 1 country.

Yotam Menuchin-LasowskiDepartment of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Röntgenstrasse 20, 48149 Münster, Germany.
André SchreiberInstitute of Virology Münster, Westfaelische Wilhelms University, Münster, Germany.
Aarón LecandaDepartment of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Röntgenstrasse 20, 48149 Münster, Germany.
Angeles Mecate-ZambranoInstitute of Virology Münster, Westfaelische Wilhelms University, Münster, Germany.
Linda BrunotteInstitute of Virology Münster, Westfaelische Wilhelms University, Münster, Germany.
Olympia E PsathakiDepartment of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Röntgenstrasse 20, 48149 Münster, Germany; Department of Biology and Center of Cellular Nanoanalytics (CellNanOs), University of Osnabrück, Barbarastrasse 11, 49076 Osnabrück, Germany.
Stephan LudwigInstitute of Virology Münster, Westfaelische Wilhelms University, Münster, Germany.
Thomas RauenDepartment of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Röntgenstrasse 20, 48149 Münster, Germany. Electronic address: thomas.rauen@mpi-muenster.mpg.de.
Hans R SchölerDepartment of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Röntgenstrasse 20, 48149 Münster, Germany. Electronic address: office@mpi-muenster.mpg.de.
Max Planck Institute for Molecular Biomedicine · DEUniversity of Münster · DEOsnabrück University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several studies have pointed to retinal involvement in COVID-19, yet many questions remain regarding the ability of SARS-CoV-2 to infect and replicate in retinal cells and its effects on the retina. Here, we have used human pluripotent stem cell-derived retinal organoids to study retinal infection by SARS-CoV-2. Indeed, SARS-CoV-2 can infect and replicate in retinal organoids, as it is shown to infect different retinal lineages, such as retinal ganglion cells and photoreceptors. SARS-CoV-2 infection of retinal organoids also induces the expression of several inflammatory genes, such as interleukin 33, a gene associated with acute COVID-19 and retinal degeneration. Finally, we show that the use of antibodies to block ACE2 significantly reduces SARS-CoV-2 infection of retinal organoids, indicating that SARS-CoV-2 infects retinal cells in an ACE2-dependent manner. These results suggest a retinal involvement in COVID-19 and emphasize the need to monitor retinal pathologies as potential sequelae of "long COVID."

Indexed as

COVID-19Angiotensin-Converting Enzyme 2HumansOrganoidsPost-Acute COVID-19 SyndromeRetinaRetinal Ganglion CellsSARS-CoV-2Angiotensin-Converting Enzyme 2COVID-19Cytokinedisease modelingInflamationiPSCsPhotoreceptorsRetinaRetinal ganglion cellsretinal organoidsSARS-CoV-2

Identifiers

PMID35334213
PMCPMC8943915
OpenAlexW4226117275

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.