Evidence map›Paper›PMID 33507952›Full record

ArticlePLoS pathogens2021

Single cell resolution of SARS-CoV-2 tropism, antiviral responses, and susceptibility to therapies in primary human airway epithelium.

Jessica K Fiege, Joshua M Thiede, Hezkiel Arya Nanda, William E Matchett, Patrick J Moore, Noe Rico Montanari, Beth K Thielen, Jerry Daniel, Emma Stanley, Ryan C Hunter and 4 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
18.7field-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

64 citing papers in PubMed, 132 citations in OpenAlex.

  1. Article
  2. Intrinsic OASL expression governs heterogeneity in interferon induction during influenza A virus infection.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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  9. Cell Culture Differentiation and Proliferation Conditions Influence theAmerican journal of respiratory cell and molecular biology · 2024
    Article
  10. Tropism for ciliated cells is the dominant driver of influenza viral burst size in the human airway.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  11. A therapy for suppressing canonical and noncanonical SARS-CoV-2 viral entry and an intrinsic intrapulmonary inflammatory response.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  12. Review
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4 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 1 country.

Jessica K FiegeCenter for Immunology, University of Minnesota, Minneapolis, Minnesota, United States of America.ORCID 0000-0002-4129-8742
Joshua M ThiedeDivision of Infectious Diseases and International Medicine, Department of Medicine, University of Minnesota, Minneapolis, Minnesota, United States of America.ORCID 0000-0002-6603-281X
Hezkiel Arya NandaInstitute for Health Informatics, University of Minnesota, Minneapolis, Minnesota, United States of America.ORCID 0000-0003-1406-1659
William E MatchettCenter for Immunology, University of Minnesota, Minneapolis, Minnesota, United States of America.ORCID 0000-0001-7515-2226
Patrick J MooreDepartment of Microbiology and Immunology, University of Minnesota, Minneapolis, Minnesota, United States of America.ORCID 0000-0003-1437-4831
Noe Rico MontanariDepartment of Microbiology and Immunology, University of Minnesota, Minneapolis, Minnesota, United States of America.ORCID 0000-0002-2211-8881
Beth K ThielenDepartment of Pediatrics, Division of Infectious Diseases, University of Minnesota, United States of America.ORCID 0000-0001-5922-0241
Jerry DanielUniversity of Minnesota Genomics Center, Minneapolis, Minnesota, United States of America.ORCID 0000-0001-9462-177X
Emma StanleyUniversity of Minnesota Genomics Center, Minneapolis, Minnesota, United States of America.ORCID 0000-0003-1566-8559
Ryan C HunterCenter for Immunology, University of Minnesota, Minneapolis, Minnesota, United States of America.ORCID 0000-0003-3841-1676
Vineet D MenacheryDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, United States of America.ORCID 0000-0001-8803-7606
Steven S ShenInstitute for Health Informatics, University of Minnesota, Minneapolis, Minnesota, United States of America.ORCID 0000-0001-7725-1260
Tyler D BoldCenter for Immunology, University of Minnesota, Minneapolis, Minnesota, United States of America.ORCID 0000-0001-7360-6546
Ryan A LangloisCenter for Immunology, University of Minnesota, Minneapolis, Minnesota, United States of America.ORCID 0000-0002-0515-571X
University of Minnesota · USThe University of Texas Medical Branch at Galveston · US

Funding

University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR002494 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R, WEISDORF, DANIEL J · 2018 to 2022
$34.9M
TRAINING-PULMONARY CELL &MOLECULAR BIOLOGY &PHYSIOLOGYT32HL007741 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI DUDLEY, R. ADAMS, INGBAR, DAVID H · 1994 to 2023
$13.9M
Infectious Disease Training in Clinical InvestigationT32AI055433 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI David R Boulware · 2003 to 2026
$6.1M
Early Responses to Influenza A Virus Replication In VivoR01AI148669 · NIAID · UNIVERSITY OF MINNESOTA · PI LANGLOIS, RYAN · 2020 to 2024
$2.5M
Identifying host and viral correlates for coronavirus pathogenesisR01AI153602 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI JOHNSON, BRYAN A · 2020 to 2023
$2.0M
The Host Genetics of Age-Dependent SusceptibilityR21AI145400 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI MENACHERY, VINEET D · 2020 to 2021
$451k
NCATS NIH HHS UL1 TR002494NHLBI NIH HHS T32 HL007741NIAID NIH HHS R01 AI148669NIAID NIH HHS R01 AI153602NIAID NIH HHS R21 AI145400NIAID NIH HHS T32 AI055433
6 · The paper itself

Abstract

The human airway epithelium is the initial site of SARS-CoV-2 infection. We used flow cytometry and single cell RNA-sequencing to understand how the heterogeneity of this diverse cell population contributes to elements of viral tropism and pathogenesis, antiviral immunity, and treatment response to remdesivir. We found that, while a variety of epithelial cell types are susceptible to infection, ciliated cells are the predominant cell target of SARS-CoV-2. The host protease TMPRSS2 was required for infection of these cells. Importantly, remdesivir treatment effectively inhibited viral replication across cell types, and blunted hyperinflammatory responses. Induction of interferon responses within infected cells was rare and there was significant heterogeneity in the antiviral gene signatures, varying with the burden of infection in each cell. We also found that heavily infected secretory cells expressed abundant IL-6, a potential mediator of COVID-19 pathogenesis.

Indexed as

Viral TropismAdenosine MonophosphateAlanineCOVID-19COVID-19 Drug TreatmentEpitheliumHumansInterferonsInterleukin-6LungSARS-CoV-2Virus ReplicationAdenosine MonophosphateAlanineInterferonsInterleukin-6remdesivir

Identifiers

PMID33507952
PMCPMC7872261
OpenAlexW3124338174

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.