Evidence map›Paper›PMID 33080984›Full record

ArticleViruses2020

Identification and Tracking of Antiviral Drug Combinations.

Aleksandr Ianevski, Rouan Yao, Svetlana Biza, Eva Zusinaite, Andres Mannik, Gaily Kivi, Anu Planken, Kristiina Kurg, Eva-Maria Tombak, Mart Ustav and 16 more

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
6.9field-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

35 citing papers in PubMed, 69 citations in OpenAlex.

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  12. Seven classes of antiviral agents.Cellular and molecular life sciences : CMLS · 2022
    Review
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  14. Article
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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

26 authors at 6 institutions in 5 countries.

Aleksandr IanevskiDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, 7028 Trondheim, Norway.
Rouan YaoDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, 7028 Trondheim, Norway.
Svetlana BizaDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, 7028 Trondheim, Norway.
Eva ZusinaiteInstitute of Technology, University of Tartu, 50090 Tartu, Estonia.
Andres MannikIcosagen Cell Factory OÜ, 61713 Kambja vald Tartumaa, Estonia.
Gaily KiviIcosagen Cell Factory OÜ, 61713 Kambja vald Tartumaa, Estonia.
Anu PlankenIcosagen Cell Factory OÜ, 61713 Kambja vald Tartumaa, Estonia.
Kristiina KurgIcosagen Cell Factory OÜ, 61713 Kambja vald Tartumaa, Estonia.
Eva-Maria TombakIcosagen Cell Factory OÜ, 61713 Kambja vald Tartumaa, Estonia.
Mart UstavIcosagen Cell Factory OÜ, 61713 Kambja vald Tartumaa, Estonia.
Nastassia ShtaidaInstitute of Technology, University of Tartu, 50090 Tartu, Estonia.
Evgeny KulesskiyInstitute for Molecular Medicine Finland, FIMM, University of Helsinki, 00014 Helsinki, Finland.
Eunji JoApplied Molecular Virology Laboratory, Institut Pasteur Korea, Sampyeong-dong 696, Bundang-gu, Seongnam-si 463-400, Gyeonggi-do, Korea.
Jaewon YangApplied Molecular Virology Laboratory, Institut Pasteur Korea, Sampyeong-dong 696, Bundang-gu, Seongnam-si 463-400, Gyeonggi-do, Korea.
Hilde LysvandDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, 7028 Trondheim, Norway.
Kirsti LøsethDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, 7028 Trondheim, Norway.
Valentyn OksenychDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, 7028 Trondheim, Norway.ORCID 0000-0002-5088-3791
Per Arne AasDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, 7028 Trondheim, Norway.
Tanel TensonInstitute of Technology, University of Tartu, 50090 Tartu, Estonia.ORCID 0000-0002-0260-3601
Astra VitkauskienėDepartment of Laboratory Medicine, Lithuanian University of Health Science, 44307 Kaunas, Lithuania.
Marc P WindischApplied Molecular Virology Laboratory, Institut Pasteur Korea, Sampyeong-dong 696, Bundang-gu, Seongnam-si 463-400, Gyeonggi-do, Korea.
Mona Høysæter FenstadDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, 7028 Trondheim, Norway.ORCID 0000-0002-9102-8409
Svein Arne NordbøDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, 7028 Trondheim, Norway.
Mart UstavIcosagen Cell Factory OÜ, 61713 Kambja vald Tartumaa, Estonia.
Magnar BjøråsDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, 7028 Trondheim, Norway.
Denis E KainovDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, 7028 Trondheim, Norway.
Norwegian University of Science and Technology · NOIcosagen (Estonia) · EEInstitut Pasteur Korea · KRUniversity of Tartu · EEUniversity of Helsinki · FILithuanian University of Health Sciences · LT

Funding

Estonian Research Competency Council MOBTT39National Research Foundation of Korea NRF-2017M3A9G6068246
6 · The paper itself

Abstract

Combination therapies have become a standard for the treatment for HIV and hepatitis C virus (HCV) infections. They are advantageous over monotherapies due to better efficacy, reduced toxicity, as well as the ability to prevent the development of resistant viral strains and to treat viral co-infections. Here, we identify new synergistic combinations against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), echovirus 1 (EV1), hepatitis C virus (HCV) and human immunodeficiency virus 1 (HIV-1) in vitro. We observed synergistic activity of nelfinavir with convalescent serum and with purified neutralizing antibody 23G7 against SARS-CoV-2 in human lung epithelial Calu-3 cells. We also demonstrated synergistic activity of nelfinavir with EIDD-2801 or remdesivir in Calu-3 cells. In addition, we showed synergistic activity of vemurafenib with emetine, homoharringtonine, anisomycin, or cycloheximide against EV1 infection in human lung epithelial A549 cells. We also found that combinations of sofosbuvir with brequinar or niclosamide are synergistic against HCV infection in hepatocyte-derived Huh-7.5 cells, and that combinations of monensin with lamivudine or tenofovir are synergistic against HIV-1 infection in human cervical TZM-bl cells. These results indicate that synergy is achieved when a virus-directed antiviral is combined with another virus- or host-directed agent. Finally, we present an online resource that summarizes novel and known antiviral drug combinations and their developmental status.

Indexed as

A549 CellsAntibodies, NeutralizingAntineoplastic AgentsAntiviral AgentsBetacoronavirusCell LineCoronavirus InfectionsCOVID-19COVID-19 Drug TreatmentDatabases, PharmaceuticalDrug CombinationsDrug DiscoveryDrug SynergismEnterovirus B, HumanHepacivirusHIV-1Antibodies, NeutralizingAntineoplastic AgentsAntiviral AgentsDrug Combinationsantiviral drug combinationsantiviralsbroad-spectrum antiviralsvirus

Identifiers

PMID33080984
PMCPMC7589631
OpenAlexW3093109568

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.