Evidence map›Paper›PMID 35906230›Full record

ArticleNature communications2022

SARS-CoV-2 VOC type and biological sex affect molnupiravir efficacy in severe COVID-19 dwarf hamster model.

Carolin M Lieber, Robert M Cox, Julien Sourimant, Josef D Wolf, Kate Juergens, Quynh Phung, Manohar T Saindane, Meghan K Smith, Zachary M Sticher, Alexander A Kalykhalov and 5 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

31 citing papers in PubMed, 50 citations in OpenAlex.

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  13. COVID-19 therapeutics.Clinical microbiology reviews · 2024
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 4 institutions in 1 country.

Carolin M Lieber *Center for Translational Antiviral Research, Institute for Biomedical Sciences, Georgia State University, Atlanta, GA, 30303, USA.
Robert M Cox *Center for Translational Antiviral Research, Institute for Biomedical Sciences, Georgia State University, Atlanta, GA, 30303, USA.ORCID 0000-0003-0620-1674
Julien SourimantCenter for Translational Antiviral Research, Institute for Biomedical Sciences, Georgia State University, Atlanta, GA, 30303, USA.ORCID 0000-0002-1660-1666
Josef D WolfCenter for Translational Antiviral Research, Institute for Biomedical Sciences, Georgia State University, Atlanta, GA, 30303, USA.ORCID 0000-0003-2507-6944
Kate JuergensVirology Division, Department of Laboratory Medicine, University of Washington, Seattle, WA, 98185, USA.
Quynh PhungVirology Division, Department of Laboratory Medicine, University of Washington, Seattle, WA, 98185, USA.
Manohar T SaindaneEmory Institute for Drug Development, Emory University, Atlanta, GA, 30329, USA.
Meghan K SmithEmory Institute for Drug Development, Emory University, Atlanta, GA, 30329, USA.ORCID 0000-0001-8491-3824
Zachary M SticherEmory Institute for Drug Development, Emory University, Atlanta, GA, 30329, USA.ORCID 0000-0002-7022-1410
Alexander A KalykhalovEmory Institute for Drug Development, Emory University, Atlanta, GA, 30329, USA.
Michael G NatchusEmory Institute for Drug Development, Emory University, Atlanta, GA, 30329, USA.
George R PainterEmory Institute for Drug Development, Emory University, Atlanta, GA, 30329, USA.
Kaori SakamotoDepartment of Pathology, College of Veterinary Medicine, University of Georgia, Athens, GA, 30602, USA.
Alexander L GreningerVirology Division, Department of Laboratory Medicine, University of Washington, Seattle, WA, 98185, USA.
Richard K PlemperCenter for Translational Antiviral Research, Institute for Biomedical Sciences, Georgia State University, Atlanta, GA, 30303, USA. rplemper@gsu.edu.ORCID 0000-0003-2034-2107
Emory University · USGeorgia State University · USUniversity of Washington · USUniversity of Georgia · US

Funding

Identification and Pre-Clinical Evaluation of Measles Virus InhibitorsR01AI071002 · NIAID · GEORGIA STATE UNIVERSITY · PI PLEMPER, RICHARD K. · 2006 to 2022
$6.6M
Development of a Broad-Spectrum Inhibitor against Seasonal and Highly-Pathogenic Influenza VirusesR01AI141222 · NIAID · GEORGIA STATE UNIVERSITY · PI PLEMPER, RICHARD K. · 2019 to 2023
$5.0M
NIAID NIH HHS R01 AI071002NIAID NIH HHS R01 AI141222
6 · The paper itself

Abstract

SARS-CoV-2 variants of concern (VOC) have triggered infection waves. Oral antivirals such as molnupiravir promise to improve disease management, but efficacy against VOC delta was questioned and potency against omicron is unknown. This study evaluates molnupiravir against VOC in human airway epithelium organoids, ferrets, and a lethal Roborovski dwarf hamster model of severe COVID-19-like lung injury. VOC were equally inhibited by molnupiravir in cells and organoids. Treatment reduced shedding in ferrets and prevented transmission. Pathogenicity in dwarf hamsters was VOC-dependent and highest for delta, gamma, and omicron. All molnupiravir-treated dwarf hamsters survived, showing reduction in lung virus load from one (delta) to four (gamma) orders of magnitude. Treatment effect size varied in individual dwarf hamsters infected with omicron and was significant in males, but not females. The dwarf hamster model recapitulates mixed efficacy of molnupiravir in human trials and alerts that benefit must be reassessed in vivo as VOC evolve.

Indexed as

COVID-19 Drug TreatmentSARS-CoV-2AnimalsCricetinaeCytidineFerretsHumansHydroxylaminesLungMaleCytidineHydroxylaminesmolnupiravir

Identifiers

PMID35906230
PMCPMC9338273
OpenAlexW4288692455

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.