Evidence map›Paper›PMID 34452519›Full record

ArticleViruses2021

Protective Effects of Astodrimer Sodium 1% Nasal Spray Formulation against SARS-CoV-2 Nasal Challenge in K18-hACE2 Mice.

Jeremy R A Paull, Carolyn A Luscombe, Alex Castellarnau, Graham P Heery, Michael D Bobardt, Philippe A Gallay

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 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
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  7. Article
  8. Article
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  13. Nasal sprays for treating COVID-19: a scientific note.Pharmacological reports : PR · 2023
    Review
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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

6 authors at 2 institutions in 2 countries.

Jeremy R A PaullStarpharma Pty Ltd., Abbotsford, VIC 3067, Australia.ORCID 0000-0002-9981-421X
Carolyn A LuscombeStarpharma Pty Ltd., Abbotsford, VIC 3067, Australia.
Alex CastellarnauStarpharma Pty Ltd., Abbotsford, VIC 3067, Australia.
Graham P HeeryStarpharma Pty Ltd., Abbotsford, VIC 3067, Australia.
Michael D BobardtDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA 92307, USA.
Philippe A GallayDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA 92307, USA.
Starpharma (Australia) · AUScripps Research Institute · US

Funding

Australian Medical Research Future Fund (MRFF) Biomedical Translation Bridge (BTB) Program BTBR300093
6 · The paper itself

Abstract

Strategies to combat COVID-19 require multiple ways to protect vulnerable people from infection. SARS-CoV-2 is an airborne pathogen and the nasal cavity is a primary target of infection. The K18-hACE2 mouse model was used to investigate the anti-SARS-CoV-2 efficacy of astodrimer sodium formulated in a mucoadhesive nasal spray. Animals received astodrimer sodium 1% nasal spray or PBS intranasally, or intranasally and intratracheally, for 7 days, and they were infected intranasally with SARS-CoV-2 after the first product administration on Day 0. Another group was infected intranasally with SARS-CoV-2 that had been pre-incubated with astodrimer sodium 1% nasal spray or PBS for 60 min before the neutralisation of test product activity. Astodrimer sodium 1% significantly reduced the viral genome copies (>99.9%) and the infectious virus (~95%) in the lung and trachea vs. PBS. The pre-incubation of SARS-CoV-2 with astodrimer sodium 1% resulted in a significant reduction in the viral genome copies (>99.9%) and the infectious virus (>99%) in the lung and trachea, and the infectious virus was not detected in the brain or liver. Astodrimer sodium 1% resulted in a significant reduction of viral genome copies in nasal secretions vs. PBS on Day 7 post-infection. A reduction in the viral shedding from the nasal cavity may result in lower virus transmission rates. Viraemia was low or undetectable in animals treated with astodrimer sodium 1% or infected with treated virus, correlating with the lack of detectable viral replication in the liver. Similarly, low virus replication in the nasal cavity after treatment with astodrimer sodium 1% potentially protected the brain from infection. Astodrimer sodium 1% significantly reduced the pro-inflammatory cytokines IL-6, IL-1α, IL-1β, TNFα and TGFβ and the chemokine MCP-1 in the serum, lung and trachea vs. PBS. Astodrimer sodium 1% nasal spray blocked or reduced SARS-CoV-2 replication and its sequelae in K18-hACE2 mice. These data indicate a potential role for the product in preventing SARS-CoV-2 infection or for reducing the severity of COVID-19.

Indexed as

COVID-19 Drug TreatmentNasal SpraysAngiotensin-Converting Enzyme 2AnimalsAntiviral AgentsBrainCOVID-19DendrimersDisease Models, AnimalFemaleLiverMaleMiceMice, TransgenicNasal CavityPolylysineACE2 protein, humanAngiotensin-Converting Enzyme 2Antiviral AgentsastodrimerDendrimersNasal SpraysPolylysineanimal modelantiviralastodrimerCOVID-19dendrimernasalSARS-CoV-2SPL7013

Identifiers

PMID34452519
PMCPMC8402925
OpenAlexW3196250664

What Socratic 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 Socratic graph.