Evidence map›Paper›PMID 34370799›Full record

ArticlePLoS pathogens2021

Intranasal type I interferon treatment is beneficial only when administered before clinical signs onset in the SARS-CoV-2 hamster model.

Pierre Bessière, Marine Wasniewski, Evelyne Picard-Meyer, Alexandre Servat, Thomas Figueroa, Charlotte Foret-Lucas, Amelia Coggon, Sandrine Lesellier, Frank Boué, Nathan Cebron and 6 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.3field-weighted citation impact, top 6% 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

40 citing papers in PubMed, 60 citations in OpenAlex.

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  13. Olfactory immune response to SARS-CoV-2.Cellular & molecular immunology · 2024
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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

16 authors at 4 institutions in 2 countries.

Pierre BessièreEcole nationale vétérinaire de Toulouse, ENVT, INRAE, UMR 1225, IHAP, Université de Toulouse, Toulouse, France.ORCID 0000-0001-5657-0027
Marine WasniewskiNancy laboratory for rabies and wildlife, ANSES, Lyssavirus Unit, Malzéville, France.ORCID 0000-0001-5054-3634
Evelyne Picard-MeyerNancy laboratory for rabies and wildlife, ANSES, Lyssavirus Unit, Malzéville, France.ORCID 0000-0001-9122-9027
Alexandre ServatNancy laboratory for rabies and wildlife, ANSES, Lyssavirus Unit, Malzéville, France.ORCID 0000-0003-4753-6614
Thomas FigueroaEcole nationale vétérinaire de Toulouse, ENVT, INRAE, UMR 1225, IHAP, Université de Toulouse, Toulouse, France.ORCID 0000-0002-4141-271X
Charlotte Foret-LucasEcole nationale vétérinaire de Toulouse, ENVT, INRAE, UMR 1225, IHAP, Université de Toulouse, Toulouse, France.
Amelia CoggonEcole nationale vétérinaire de Toulouse, ENVT, INRAE, UMR 1225, IHAP, Université de Toulouse, Toulouse, France.ORCID 0000-0001-9543-7317
Sandrine LesellierNancy laboratory for rabies and wildlife, ANSES, Atton experimental facility, Atton, France.
Frank BouéNancy laboratory for rabies and wildlife, ANSES, Lyssavirus Unit, Malzéville, France.ORCID 0000-0003-0957-1320
Nathan CebronEcole nationale vétérinaire de Toulouse, ENVT, INRAE, UMR 1225, IHAP, Université de Toulouse, Toulouse, France.
Blandine GausserèsEcole nationale vétérinaire de Toulouse, ENVT, INRAE, UMR 1225, IHAP, Université de Toulouse, Toulouse, France.
Catherine TrumelEcole nationale vétérinaire de Toulouse, ENVT, CREFRE, INSERM, Université de Toulouse, Toulouse, France.ORCID 0000-0001-9717-5808
Gilles FoucrasEcole nationale vétérinaire de Toulouse, ENVT, INRAE, UMR 1225, IHAP, Université de Toulouse, Toulouse, France.ORCID 0000-0002-0363-0337
Francisco J SalgueroNational Infection Service, Public Health England (PHE), Porton Down, Salisbury, Wiltshire, United Kingdom.ORCID 0000-0002-5315-3882
Elodie Monchatre-LeroyNancy laboratory for rabies and wildlife, ANSES, Lyssavirus Unit, Malzéville, France.ORCID 0000-0002-3231-398X
Romain VolmerEcole nationale vétérinaire de Toulouse, ENVT, INRAE, UMR 1225, IHAP, Université de Toulouse, Toulouse, France.
École Nationale Vétérinaire de Toulouse · FROffice National de la Chasse et de la Faune Sauvage · FRInserm · FRPublic Health England · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Impaired type I interferons (IFNs) production or signaling have been associated with severe COVID-19, further promoting the evaluation of recombinant type I IFNs as therapeutics against SARS-CoV-2 infection. In the Syrian hamster model, we show that intranasal administration of IFN-α starting one day pre-infection or one day post-infection limited weight loss and decreased viral lung titers. By contrast, intranasal administration of IFN-α starting at the onset of symptoms three days post-infection had no impact on the clinical course of SARS-CoV-2 infection. Our results provide evidence that early type I IFN treatment is beneficial, while late interventions are ineffective, although not associated with signs of enhanced disease.

Indexed as

COVID-19 Drug TreatmentAdministration, IntranasalAnimalsAntiviral AgentsChlorocebus aethiopsCricetinaeDisease Models, AnimalInterferon Type IMesocricetusSARS-CoV-2Antiviral AgentsInterferon Type I

Identifiers

PMID34370799
PMCPMC8376007
OpenAlexW3191057636

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.