Evidence map›Paper›PMID 32559285›Full record

ArticleThe Journal of infectious diseases2020

Interferon-β-1a Inhibition of Severe Acute Respiratory Syndrome-Coronavirus 2 In Vitro When Administered After Virus Infection.

Nicola Clementi, Roberto Ferrarese, Elena Criscuolo, Roberta Antonia Diotti, Matteo Castelli, Carolina Scagnolari, Roberto Burioni, Guido Antonelli, Massimo Clementi, Nicasio Mancini

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
–field-weighted citation impact
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

45 citing papers in PubMed.

  1. An open-label randomized controlled trial of the effect of lopinavir/ritonavir, lopinavir/ritonavir plus IFN-β-1a and hydroxychloroquine in hospitalized patients with COVID-19.Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases · 2021
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  9. Association ofInterdisciplinary perspectives on infectious diseases · 2023
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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

10 authors.

Nicola ClementiLaboratory of Microbiology and Virology, Università Vita-Salute San Raffaele, Milan, Italy.
Roberto FerrareseLaboratory of Microbiology and Virology, Università Vita-Salute San Raffaele, Milan, Italy.
Elena CriscuoloLaboratory of Microbiology and Virology, Università Vita-Salute San Raffaele, Milan, Italy.
Roberta Antonia DiottiLaboratory of Microbiology and Virology, Università Vita-Salute San Raffaele, Milan, Italy.
Matteo CastelliLaboratory of Microbiology and Virology, Università Vita-Salute San Raffaele, Milan, Italy.
Carolina ScagnolariLaboratory of Virology, Department of Molecular Medicine, and Institute Pasteur Italia-Cenci Bolognetti Foundation, Sapienza University, Rome, Italy.
Roberto BurioniLaboratory of Microbiology and Virology, Università Vita-Salute San Raffaele, Milan, Italy.
Guido AntonelliLaboratory of Virology, Department of Molecular Medicine, and Institute Pasteur Italia-Cenci Bolognetti Foundation, Sapienza University, Rome, Italy.
Massimo ClementiLaboratory of Microbiology and Virology, Università Vita-Salute San Raffaele, Milan, Italy.
Nicasio ManciniLaboratory of Microbiology and Virology, Università Vita-Salute San Raffaele, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ongoing coronavirus disease 2019 pandemic has forced the clinical and scientific community to try drug repurposing of existing antiviral agents as a quick option against severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2). Under this scenario, interferon (IFN) β-1a, whose antiviral potential is already known, and which is a drug currently used in the clinical management of multiple sclerosis, may represent as a potential candidate. In this report, we demonstrate that IFN-β-1a was highly effective in inhibiting in vitro SARS-CoV-2 replication at clinically achievable concentration when administered after virus infection.

Indexed as

AnimalsAntiviral AgentsBetacoronavirusChlorocebus aethiopsCoronavirus InfectionsCOVID-19Drug RepositioningInterferon beta-1aPandemicsPneumonia, ViralSARS-CoV-2Vero CellsVirus ReplicationAntiviral AgentsInterferon beta-1aCOVID-19 clinical trialIFN-β-1aSARS-CoV-2

Identifiers

PMID32559285
PMCPMC7337790

What OpenQuestion holds

Textmetadata
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.