Literature DB >> 24091203

Host-targeting agents in the treatment of hepatitis C: a beginning and an end?

James M Baugh1, Jose A Garcia-Rivera, Philippe A Gallay.   

Abstract

The development of two distinct classes of hepatitis C antiviral agents, direct-acting antivirals (DAAs) and host-targeting antivirals (HTAs), have distinctly impacted the hepatitis C virus (HCV) field by generating higher sustained virological response (SVR) rates within infected patients, via reductions in both adverse side effects and duration of treatment when compared to the old standard of care. Today DAAs are actively incorporated into the standard of care and continue to receive the most advanced clinical trial analysis. With a multitude of innovative and potent second-generation DAA compounds currently being tested in clinical trials, it is clear that the future of DAAs looks very bright. In comparison to the other class of compounds, HTAs have been slightly less impactful, despite the fact that primary treatment regimens for HCV began with the use of an HTA - interferon alpha (IFNα). The compound was advantageous in that it provided a broad-reaching antiviral response; however deleterious side effects and viral/patient resistance has since made the compound outdated. HTA research has since moved onward to target a number of cellular host factors that are required for HCV viral entry and replication such as scavenger receptor-BI (SR-BI), 3-hydroxy-3-methyl-glutaryl-CoA reductase (HMGCoA reductase), cyclophilin A (CypA), fatty acid synthase (FASN) and miRNA-122. The rationale behind pursuing these HTAs is based upon the extremely low mutational rate that occurs within eukaryotic cells, thereby creating a high genetic barrier to drug resistance for anti-HCV compounds, as well as pan-genotypic coverage to all HCV genotypes and serotypes. As the end appears near for HCV, it becomes important to ask if the development of novel HTAs should also be analyzed in combination with other DAAs, in order to address potential hard-to-treat HCV patient populations. Since the treatment regimens for HCV began with the use of a global HTA, could one end the field as well?
Copyright © 2013 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Alisporivir; Cyclophilin A; HCV; Host-targeting antivirals

Mesh:

Substances:

Year:  2013        PMID: 24091203      PMCID: PMC3971122          DOI: 10.1016/j.antiviral.2013.09.020

Source DB:  PubMed          Journal:  Antiviral Res        ISSN: 0166-3542            Impact factor:   5.970


  68 in total

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Review 3.  Interferon-lambda: a new addition to an old family.

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4.  Treatment of HCV infection by targeting microRNA.

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Journal:  N Engl J Med       Date:  2013-03-27       Impact factor: 91.245

5.  The use of AlphaLISA technology to detect interaction between hepatitis C virus-encoded NS5A and cyclophilin A.

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Authors:  Udayan Chatterji; Precious Lim; Michael D Bobardt; Stefan Wieland; Daniel G Cordek; Gregoire Vuagniaux; Francis Chisari; Craig E Cameron; Paul Targett-Adams; Tanya Parkinson; Philippe A Gallay
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Authors:  Philippe A Gallay; Kai Lin
Journal:  Drug Des Devel Ther       Date:  2013-02-15       Impact factor: 4.162

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2.  Hepatitis C Virus-Induced Rab32 Aggregation and Its Implications for Virion Assembly.

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Review 3.  Monoclonal antibodies: Principles and applications of immmunodiagnosis and immunotherapy for hepatitis C virus.

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Authors:  L B Dustin; B Bartolini; M R Capobianchi; M Pistello
Journal:  Clin Microbiol Infect       Date:  2016-08-31       Impact factor: 8.067

5.  Identification of a novel epitope in the C terminus of hepatitis C virus-E2 protein that induces potent and cross-reactive neutralizing antibodies.

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Review 7.  Genetic variants at the IFNL3 locus and their association with hepatitis C virus infections reveal novel insights into host-virus interactions.

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Review 9.  Direct-acting antiviral agents for hepatitis C: structural and mechanistic insights.

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Journal:  Nat Rev Gastroenterol Hepatol       Date:  2016-05-05       Impact factor: 46.802

10.  Seed sequence-matched controls reveal limitations of small interfering RNA knockdown in functional and structural studies of hepatitis C virus NS5A-MOBKL1B interaction.

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