Cited by 122Influenza Virus Research StudiesRespiratory viral infections researchComputational Drug Discovery Methods

The DOI matches its Crossref record; 117 of the 117 references it cites were found in a registry or an index.

Drug Repurposing Approaches for the Treatment of Influenza Viral Infection: Reviving Old Drugs to Fight Against a Long-Lived Enemy

Open access
Pizzorno, Andrés, Padey, Blandine, Terrier, Olivier, Rosa-Calatrava, Manuel·2019·Frontiers in Immunology

Abstract

Influenza viruses still constitute a real public health problem today. To cope with the emergence of new circulating strains, but also the emergence of resistant strains to classic antivirals, it is necessary to develop new antiviral approaches. This review summarizes the state-of-the-art of current antiviral options against influenza infection, with particular focus on the recent advances of anti-influenza drug repurposing strategies and their potential therapeutic, regulatory and economic benefits. The review will illustrate the multiple ways to reposition molecules for the treatment of influenza, from adventitious discovery to in silico-based screening. These novel antiviral molecules, many of which targeting the host cell, in combination with conventional antiviral agents targeting the virus, will ideally enter the clinics and reinforce the therapeutic arsenal to combat influenza virus infections.

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Crossref · 10.3389/fimmu.2019.00531

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Figure 1 From the bench to the bedside: comparison between de novo drug development and drug repurposing. De novo (classic) drug development constitutes a time-consuming and expensive process. From initial discovery to market, it generally takes 13–15 years and costs up to US$ 2 billion, with a very low success rate (10%). In contrast, drug repurposing approaches offer several advantages. Indeed, the time frame from discovery to market is shorter (5–11 years), less expensive (US$ 350 million), and with a higher success rate (30%), mostly because a large part of preclinical and clinical testings (e.g., safety, formulation, posology) have been already performed for the drug's initial therapeutic indication (41, 42).
Figure 1 From the bench to the bedside: comparison between de novo drug development and drug repurposing. De novo (classic) drug development constitutes a time-consuming and expensive process. From initial discovery to market, it generally takes 13–15 years and costs up to US$ 2 billion, with a very low success rate (10%). In contrast, drug repurposing approaches offer several advantages. Indeed, the time frame from discovery to market is shorter (5–11 years), less expensive (US$ 350 million), and with a higher success rate (30%), mostly because a large part of preclinical and clinical testings (e.g., safety, formulation, posology) have been already performed for the drug's initial therapeutic indication (41, 42).CC BY · PubMed Central

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Cited by

Sorted by citations

  • Discovery and development of safe-in-man broad-spectrum antiviral agents

    Andersen, P. I., Ianevski, A., Lysvand, H., Vitkauskienė, A., Oksenych, V., Bjørås, M., Telling, K., Lutsar, I., Dumpis, U., Irie, Y., et al. (2020) · International Journal of Infectious Diseases · doi:10.1016/j.ijid.2020.02.018 · Cited by 274

    “…opportunities, including a substantially higher probability of success to market as compared with developing new virus-specific drugs and vaccines, and a significantly reduced cost and timeline to clinical availability (Ianevski et al., 2019; Pizzorno et al., 2019; Zheng et al., 2018).”
  • Host-Directed Antiviral Therapy

    Kumar, N., Sharma, S., Kumar, R., Tripathi, B. N., Barua, S., Ly, H., & Rouse, B. T. (2020) · Clinical Microbiology Reviews · doi:10.1128/cmr.00168-19 · Cited by 289

    “multiple host factors and pathways that are supportive of virus replication (299, 300).”
    Background
  • Antiviral Approaches against Influenza Virus

    Kumari, R., Sharma, S. D., Kumar, A., Ende, Z. S., Mishina, M., Wang, Y., Falls, Z., Samudrala, R., Pohl, J., Knight, P. R., et al. (2023) · Clinical Microbiology Reviews · doi:10.1128/cmr.00040-22 · Cited by 176

    “It was demonstrated in vitro and in vivo in a mouse model that Diltiazem modulates host antiviral genes in vitro and in vivo in a mouse model, and cotreatment with Oseltamivir enhanced the antiviral efficacy (362).”
    Background
  • Inhibitors of VPS34 and fatty-acid metabolism suppress SARS-CoV-2 replication

    Williams, C. G., Jureka, A. S., Silvas, J. A., Nicolini, A. M., Chvatal, S. A., Carlson-Stevermer, J., Oki, J., Holden, K., & Basler, C. F. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109479 · Cited by 143

    “Repurposing drugs developed for other diseases and conditions may provide a shortcut to antiviral development (Garcı́a-Serradilla et al., 2019; Li and De Clercq, 2020; Pizzorno et al., 2019; Saini et al., 2020).”
  • Potential Antiviral Options against SARS-CoV-2 Infection

    Ianevski, A., Yao, R., Fenstad, M. H., Biza, S., Žusinaite, E., Reisberg, T., Lysvand, H., Løseth, K., Landsem, V. M., Malmring, J. F., et al. (2020) · Viruses · doi:10.3390/v12060642 · Cited by 104

See all 122

Metadata

Authors
Pizzorno, A., Padey, B., Terrier, O., & Rosa-Calatrava, M.
Affiliations
Lyon 1 Université (FR)
Corresponding author
Terrier, Olivier
Venue
Frontiers in Immunology
Published
2019-03-19
Volume
10
Pages
531-531
ISSN
1664-3224 (ISSN-L)
OpenAlex
W2923800168
Cited by
122
References
117
Citations by year
2026: 2 · 2025: 13 · 2024: 12 · 2023: 11 · 2022: 17 · 2021: 24 · 2020: 38 · 2019: 5
FWCI
3.06
Type
journal article
Language
en
Open access
Locations
  • Frontiers in Immunology (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • HAL (submittedVersion, other-oa)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
Région Auvergne-Rhône-Alpes
Topics
  • Health Sciences › Medicine › Epidemiology › Influenza Virus Research Studies
  • Health Sciences › Medicine › Epidemiology › Respiratory viral infections research
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Drug Discovery › Computational Drug Discovery Methods
Keywords
drug repurposing, influenza virus, antiviral agents, host-targeted antivirals, antiviral resistance, virtual screening, antiviral drug discovery
MeSH terms
Animals, Antiviral Agents, Humans, Influenza, Human, Orthomyxoviridae, Orthomyxoviridae Infections, Drug Repositioning

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