Evidence map›Paper›PMID 32665127›Full record

ReviewCytokine & growth factor reviews2020

Are we fully exploiting type I Interferons in today's fight against COVID-19 pandemic?

Eleonora Aricò, Laura Bracci, Luciano Castiello, Sandra Gessani, Filippo Belardelli

Abstract readReview
In one paragraph

Review in Cytokine & growth factor reviews, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
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  8. MnScience signaling · 2021
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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

5 authors.

Eleonora AricòFaBioCell, Core Facilities, Istituto Superiore di Sanità, Rome, Italy.
Laura BracciDepartment of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome, Italy.
Luciano CastielloFaBioCell, Core Facilities, Istituto Superiore di Sanità, Rome, Italy.
Sandra GessaniCenter for Gender-specific Medicine, Istituto Superiore di Sanità, Rome, Italy.
Filippo BelardelliInstitute of Translational Pharmacology, Consiglio Nazionale delle Ricerche, Rome, Italy. Electronic address: filippo.belardelli@ift.cnr.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coronavirus disease 2019 (COVID-19) first emerged in late 2019 in China. At the time of writing, its causative agent SARS-CoV-2 has spread worldwide infecting over 9 million individuals and causing more than 460,000 deaths. In the absence of vaccines, we are facing the dramatic challenge of controlling COVID-19 pandemic. Among currently available drugs, type I Interferons (IFN-I) - mainly IFN-α and β -represent ideal candidates given their direct and immune-mediated antiviral effects and the long record of clinical use. However, the best modalities of using these cytokines in SARS-CoV-2 infected patients is a matter of debate. Here, we discuss how we can exploit the current knowledge on IFN-I system to tailor the most promising dosing, timing and route of administration of IFN-I to the disease stage, with the final aim of making these cytokines a valuable therapeutic strategy in today's fight against COVID-19 pandemic.

Indexed as

Antiviral AgentsBetacoronavirusCoronavirus InfectionsCOVID-19HumansImmunotherapyInterferon-alphaInterferon-betaPandemicsPneumonia, ViralSARS-CoV-2Secondary PreventionAntiviral AgentsInterferon-alphaInterferon-betaAntiviral Immune ResponseAntiviral therapyBeta InterferonCoronavirusCOVID-19ImmunomodulationMucosal treatmentsSARS-CoV-2Type I Interferons

Identifiers

PMID32665127
PMCPMC7334951

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.