Eradication of persistent coxsackievirus B infection from a pancreatic cell line with clinically used antiviral drugs.


Journal

Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology
ISSN: 1873-5967
Titre abrégé: J Clin Virol
Pays: Netherlands
ID NLM: 9815671

Informations de publication

Date de publication:
07 2020
Historique:
received: 13 10 2019
revised: 06 03 2020
accepted: 23 03 2020
pubmed: 26 5 2020
medline: 2 7 2021
entrez: 26 5 2020
Statut: ppublish

Résumé

Persistent enterovirus infections create a difficult therapeutic challenge in immunocompromised patients and may also contribute to the development of chronic diseases including type 1 diabetes, cardiomyopathies, post-polio syndrome and chronic fatigue syndrome. To study the ability of antiviral drugs to eradicate such infection in vitro to evalaute their potential in the treatments of these patients. We set out to evaluate several licensed or clinically tested drugs which have shown some anti-enterovirus activity in previous studies for their ability to cure persistent infection established by two different coxsackievirus B1 strains in a pancreatic cell line (PANC-1 cells). Among all tested drugs Enviroxime, Fluoxetine, concentrated human IgG product (Hizentra) and Pleconaril were able to eradicate persistent Coxsackievirus B1 infection. The effect Enviroxime, Hizentra and Pleconaril varied between the two virus strains. The identified drugs are feasible candidates for clinical trials among patients with persistent coxsackievirus B infections or chronic enterovirus-associated diseases.

Sections du résumé

BACKGROUND
Persistent enterovirus infections create a difficult therapeutic challenge in immunocompromised patients and may also contribute to the development of chronic diseases including type 1 diabetes, cardiomyopathies, post-polio syndrome and chronic fatigue syndrome.
OBJECTIVES
To study the ability of antiviral drugs to eradicate such infection in vitro to evalaute their potential in the treatments of these patients.
STUDY DESIGN
We set out to evaluate several licensed or clinically tested drugs which have shown some anti-enterovirus activity in previous studies for their ability to cure persistent infection established by two different coxsackievirus B1 strains in a pancreatic cell line (PANC-1 cells).
RESULTS
Among all tested drugs Enviroxime, Fluoxetine, concentrated human IgG product (Hizentra) and Pleconaril were able to eradicate persistent Coxsackievirus B1 infection. The effect Enviroxime, Hizentra and Pleconaril varied between the two virus strains.
CONCLUSIONS
The identified drugs are feasible candidates for clinical trials among patients with persistent coxsackievirus B infections or chronic enterovirus-associated diseases.

Identifiants

pubmed: 32450550
pii: S1386-6532(20)30076-7
doi: 10.1016/j.jcv.2020.104334
pii:
doi:

Substances chimiques

Antiviral Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

104334

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest I declare no conflict of interest and I approved the final manuscript.

Auteurs

Anni Honkimaa (A)

Tampere University, Faculty of Medicine and Health Technology, Arvo Ylpönkatu 34, FIN-33520 Tampere, Finland. Electronic address: anni.honkimaa@tuni.fi.

Amir-Babak Sioofy-Khojine (AB)

Tampere University, Faculty of Medicine and Health Technology, Arvo Ylpönkatu 34, FIN-33520 Tampere, Finland.

Sami Oikarinen (S)

Tampere University, Faculty of Medicine and Health Technology, Arvo Ylpönkatu 34, FIN-33520 Tampere, Finland.

Antoine Bertin (A)

Université de Lille, CHU Lille Laboratoire de Virologie, EA3610, F-59000 Lille, France.

Didier Hober (D)

Université de Lille, CHU Lille Laboratoire de Virologie, EA3610, F-59000 Lille, France.

Heikki Hyöty (H)

Tampere University, Faculty of Medicine and Health Technology, Arvo Ylpönkatu 34, FIN-33520 Tampere, Finland; Fimlab Laboratories, Pirkanmaa Hospital District, Tampere, Finland.

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Classifications MeSH