Evidence map›Paper›PMID 34578348›Full record

ArticleViruses2021

Nafamostat-Interferon-α Combination Suppresses SARS-CoV-2 Infection In Vitro and In Vivo by Cooperatively Targeting Host TMPRSS2.

Aleksandr Ianevski, Rouan Yao, Hilde Lysvand, Gunnveig Grødeland, Nicolas Legrand, Valentyn Oksenych, Eva Zusinaite, Tanel Tenson, Magnar Bjørås, Denis E Kainov

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  7. Seven classes of antiviral agents.Cellular and molecular life sciences : CMLS · 2022
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Proteolysis and Deficiency of α1-Proteinase Inhibitor in SARS-CoV-2 Infection.Biochemistry (Moscow) Supplement. Series B, Biomedical chemistry · 2022
    Article
  14. Review
  15. Article
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

10 authors at 4 institutions in 3 countries.

Aleksandr IanevskiDepartment of Clinical and Molecular Medicine (IKOM), Norwegian University of Science and Technology, 7028 Trondheim, Norway.
Rouan YaoDepartment of Clinical and Molecular Medicine (IKOM), Norwegian University of Science and Technology, 7028 Trondheim, Norway.
Hilde LysvandDepartment of Clinical and Molecular Medicine (IKOM), Norwegian University of Science and Technology, 7028 Trondheim, Norway.
Gunnveig GrødelandResearch Institute of Internal Medicine, Oslo University Hospital Rikshospitalet, 0372 Oslo, Norway.
Nicolas LegrandOncodesign, 25 Avenue du Québec, 91140 Villebon Sur Yvette, France.
Valentyn OksenychDepartment of Clinical and Molecular Medicine (IKOM), Norwegian University of Science and Technology, 7028 Trondheim, Norway.ORCID 0000-0002-5088-3791
Eva ZusinaiteInstitute of Technology, University of Tartu, 50411 Tartu, Estonia.
Tanel TensonInstitute of Technology, University of Tartu, 50411 Tartu, Estonia.ORCID 0000-0002-0260-3601
Magnar BjøråsDepartment of Clinical and Molecular Medicine (IKOM), Norwegian University of Science and Technology, 7028 Trondheim, Norway.ORCID 0000-0001-8759-1170
Denis E KainovDepartment of Clinical and Molecular Medicine (IKOM), Norwegian University of Science and Technology, 7028 Trondheim, Norway.ORCID 0000-0001-7716-6955
Norwegian University of Science and Technology · NOUniversity of Tartu · EEOslo University Hospital · NOUniversity of Helsinki · FI

Funding

Estonian Research Competency Council MOBTT39
6 · The paper itself

Abstract

SARS-CoV-2 and its vaccine/immune-escaping variants continue to pose a serious threat to public health due to a paucity of effective, rapidly deployable, and widely available treatments. Here, we address these challenges by combining Pegasys (IFNα) and nafamostat to effectively suppress SARS-CoV-2 infection in cell culture and hamsters. Our results indicate that Serpin E1 is an important mediator of the antiviral activity of IFNα and that both Serpin E1 and nafamostat can target the same cellular factor TMPRSS2, which plays a critical role in viral replication. The low doses of the drugs in combination may have several clinical advantages, including fewer adverse events and improved patient outcome. Thus, our study may provide a proactive solution for the ongoing pandemic and potential future coronavirus outbreaks, which is still urgently required in many parts of the world.

Indexed as

AnimalsAnti-Inflammatory Agents, Non-SteroidalBenzamidinesCOVID-19COVID-19 Drug TreatmentCricetinaeDisease Models, AnimalDrug Therapy, CombinationFemaleGuanidinesHost-Pathogen InteractionsHumansInterferon-alphaSARS-CoV-2Serine EndopeptidasesVirus ReplicationAnti-Inflammatory Agents, Non-SteroidalBenzamidinesGuanidinesInterferon-alphanafamostatSerine EndopeptidasesTMPRSS2 protein, humanantiviral drug combinationbroad-spectrum antiviralsinterferon-alphanafamostatSARS-CoV-2

Identifiers

PMID34578348
PMCPMC8473362
OpenAlexW3196559249

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.