Evidence mapPaperPMID 39000315Full record

ReviewInternational journal of molecular sciences2024

Aprotinin (II): Inhalational Administration for the Treatment of COVID-19 and Other Viral Conditions.

Juan-Fernando Padín, José Manuel Pérez-Ortiz, Francisco Javier Redondo-Calvo

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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

3 authors.

Juan-Fernando PadínDepartment of Medical Sciences, School of Medicine at Ciudad Real, University of Castilla-La Mancha, 13971 Ciudad Real, Spain.ORCID 0000-0003-4585-9401
José Manuel Pérez-OrtizFacultad HM de Ciencias de la Salud, Universidad Camilo José Cela, 28692 Madrid, Spain.ORCID 0000-0002-3588-6273
Francisco Javier Redondo-CalvoDepartment of Medical Sciences, School of Medicine at Ciudad Real, University of Castilla-La Mancha, 13971 Ciudad Real, Spain.ORCID 0000-0002-7044-0154

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aprotinin is a broad-spectrum inhibitor of human proteases that has been approved for the treatment of bleeding in single coronary artery bypass surgery because of its potent antifibrinolytic actions. Following the outbreak of the COVID-19 pandemic, there was an urgent need to find new antiviral drugs. Aprotinin is a good candidate for therapeutic repositioning as a broad-spectrum antiviral drug and for treating the symptomatic processes that characterise viral respiratory diseases, including COVID-19. This is due to its strong pharmacological ability to inhibit a plethora of host proteases used by respiratory viruses in their infective mechanisms. The proteases allow the cleavage and conformational change of proteins that make up their viral capsid, and thus enable them to anchor themselves by recognition of their target in the epithelial cell. In addition, the activation of these proteases initiates the inflammatory process that triggers the infection. The attraction of the drug is not only its pharmacodynamic characteristics but also the possibility of administration by the inhalation route, avoiding unwanted systemic effects. This, together with the low cost of treatment (≈2 Euro/dose), makes it a good candidate to reach countries with lower economic means. In this article, we will discuss the pharmacodynamic, pharmacokinetic, and toxicological characteristics of aprotinin administered by the inhalation route; analyse the main advances in our knowledge of this medication; and the future directions that should be taken in research in order to reposition this medication in therapeutics.

Indexed as

Antiviral AgentsAprotininCOVID-19 Drug TreatmentSARS-CoV-2Administration, InhalationAnimalsCOVID-19Drug RepositioningHumansSerine Proteinase InhibitorsAntiviral AgentsAprotininSerine Proteinase Inhibitorsangiotensin-converting enzyme type 2 (ACE2)antifibrinolyticaprotininCOVID-19inhalational administrationkinin–kallikrein system (KKS)pharmacodynamicpharmacokineticproteasesrenin–angiotensin–aldosterone system (RAAS)

Identifiers

PMID39000315
PMCPMC11241800

What Socratic holds

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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.