Evidence map›Paper›PMID 36880581›Full record

ArticleEMBO reports2023

Interferon-induced transmembrane protein 3 (IFITM3) limits lethality of SARS-CoV-2 in mice.

Adam D Kenney, Ashley Zani, Jeffrey Kawahara, Adrian C Eddy, Xiao-Liang Wang, K C Mahesh, Mijia Lu, Jeronay Thomas, Jacob E Kohlmeier, Mehul S Suthar and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in EMBO reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
5.9field-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

32 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
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  6. Review
  7. MARCH E3 Ligases: Understudied Regulators of Pulmonary Immune Function.Journal of respiratory biology and translational medicine · 2026
    Article
  8. Article
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  12. mBio · 2025
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 3 institutions in 1 country.

Adam D Kenney *Department of Microbial Infection and Immunity, The Ohio State University, Columbus, OH, USA.ORCID 0000-0002-9110-1178
Ashley Zani *Department of Microbial Infection and Immunity, The Ohio State University, Columbus, OH, USA.
Jeffrey KawaharaDepartment of Microbial Infection and Immunity, The Ohio State University, Columbus, OH, USA.
Adrian C EddyDepartment of Microbial Infection and Immunity, The Ohio State University, Columbus, OH, USA.ORCID 0000-0002-9945-2810
Xiao-Liang WangDepartment of Surgery, The Ohio State University, Columbus, OH, USA.
K C MaheshInfectious Diseases Institute, The Ohio State University, Columbus, OH, USA.
Mijia LuInfectious Diseases Institute, The Ohio State University, Columbus, OH, USA.
Jeronay ThomasDepartment of Microbiology and Immunology, Emory University, Atlanta, GA, USA.
Jacob E KohlmeierDepartment of Microbiology and Immunology, Emory University, Atlanta, GA, USA.
Mehul S SutharDepartment of Microbiology and Immunology, Emory University, Atlanta, GA, USA.
Emily A HemannDepartment of Microbial Infection and Immunity, The Ohio State University, Columbus, OH, USA.
Jianrong LiInfectious Diseases Institute, The Ohio State University, Columbus, OH, USA.
Mark E PeeplesInfectious Diseases Institute, The Ohio State University, Columbus, OH, USA.
Luanne Hall-StoodleyDepartment of Microbial Infection and Immunity, The Ohio State University, Columbus, OH, USA.ORCID 0000-0003-2531-4797
Adriana ForeroDepartment of Microbial Infection and Immunity, The Ohio State University, Columbus, OH, USA.ORCID 0000-0002-2698-658X
Chuanxi CaiDepartment of Surgery, The Ohio State University, Columbus, OH, USA.
Jianjie MaDepartment of Surgery, The Ohio State University, Columbus, OH, USA.
Jacob S YountDepartment of Microbial Infection and Immunity, The Ohio State University, Columbus, OH, USA.ORCID 0000-0002-6128-4575
The Ohio State University · USEmory University · USNationwide Children's Hospital · US

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
Project 3: Responding to Changing Serological and Viral Information around COVID-19 (RESPOND)U54CA260582 · NCI · OHIO STATE UNIVERSITY · PI MCALEARNEY, ANN SCHECK, OLTZ, EUGENE M · 2020 to 2024
$10.4M
Training a New Generation of VaccinologistsT32AI074492 · NIAID · EMORY UNIVERSITY · PI Rama Rao Amara, Benjamin A Lopman · 2009 to 2026
$6.4M
Cellular and molecular programming of lung resident T cell memoryR35HL150803 · NHLBI · EMORY UNIVERSITY · PI JACOB E KOHLMEIER · 2020 to 2026
$5.4M
Mechanisms of innate resistance to virus infectionsR01AI130110 · NIAID · OHIO STATE UNIVERSITY · PI Jacob Yount · 2017 to 2026
$4.3M
THE ROLE OF THE NON-CANONICAL INFLAMMASOME IN INNATE IMMUNITYR01AI159452 · NIAID · OHIO STATE UNIVERSITY · PI AMER, AMAL O, SEVEAU, STEPHANIE M M · 2021 to 2025
$3.7M
Mechanisms of lung and cardiac pathology in SARS-CoV-2 infectionsR01HL168501 · NHLBI · OHIO STATE UNIVERSITY · PI Amal O Amer, Jacob Yount · 2023 to 2026
$2.9M
Protein therapy to treat virus induced cardiopulmonary injuryR01HL157215 · NHLBI · UNIVERSITY OF VIRGINIA · PI CAI, CHUANXI, MA, JIANJIE · 2022 to 2025
$2.7M
Mechanistic characterization of a new master regulator of cardiac virus infectionsR01HL154001 · NHLBI · OHIO STATE UNIVERSITY · PI ACCORNERO, FEDERICA, YOUNT, JACOB · 2020 to 2023
$2.3M
Interdisciplinary Program in Microbe-Host BiologyT32AI165391 · NIAID · OHIO STATE UNIVERSITY · PI RAJENDAR K DEORA, Daniel J Wozniak · 2022 to 2026
$1.5M
Establishing a relevant mouse model with susceptibility to non-adapted influenza viruses for vaccine challenge studiesR21AI151230 · NIAID · OHIO STATE UNIVERSITY · PI YOUNT, JACOB · 2020 to 2021
$409k
Mechanisms of Interferon-Lambda Programming at the Innate-Adaptive Immune Interface for Protection Against Virus InfectionK22AI146141 · NIAID · OHIO STATE UNIVERSITY · PI HEMANN, EMILY ANN · 2021 to 2022
$268k
NCI NIH HHS U54 CA260582NHLBI NIH HHS R01 HL154001NHLBI NIH HHS R01 HL157215NHLBI NIH HHS R01 HL168501NHLBI NIH HHS R35 HL150803NIAID NIH HHS K22 AI146141NIAID NIH HHS R01 AI130110NIAID NIH HHS R01 AI159452NIAID NIH HHS R21 AI151230NIAID NIH HHS T32 AI074492NIAID NIH HHS T32 AI165391NIH HHS P51 OD011132
6 · The paper itself

Abstract

Interferon-induced transmembrane protein 3 (IFITM3) is an antiviral protein that alters cell membranes to block fusion of viruses. Conflicting reports identified opposing effects of IFITM3 on SARS-CoV-2 infection of cells, and its impact on viral pathogenesis in vivo remains unclear. Here, we show that IFITM3 knockout (KO) mice infected with SARS-CoV-2 experience extreme weight loss and lethality compared to mild infection in wild-type (WT) mice. KO mice have higher lung viral titers and increases in inflammatory cytokine levels, immune cell infiltration, and histopathology. Mechanistically, we observe disseminated viral antigen staining throughout the lung and pulmonary vasculature in KO mice, as well as increased heart infection, indicating that IFITM3 constrains dissemination of SARS-CoV-2. Global transcriptomic analysis of infected lungs shows upregulation of gene signatures associated with interferons, inflammation, and angiogenesis in KO versus WT animals, highlighting changes in lung gene expression programs that precede severe lung pathology and fatality. Our results establish IFITM3 KO mice as a new animal model for studying severe SARS-CoV-2 infection and overall demonstrate that IFITM3 is protective in SARS-CoV-2 infections in vivo.

Indexed as

COVID-19SARS-CoV-2AnimalsInterferonsLungMembrane ProteinsMiceMice, Knockoutfragilis protein, mouseInterferonsMembrane ProteinsCOVID-19IFITMIFITM3interferonSARS-CoV-2

Identifiers

PMID36880581
PMCPMC10074051
OpenAlexW4323347928

What OpenQuestion holds

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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 OpenQuestion graph.