Literature DB >> 19275702

New drug targets for hepatitis C and other Flaviviridae viruses.

Tuma Paula1, Rivas Pablo, Vispo Eugenia, Barreiro Pablo, Puente Sabino, Medrano José, Madejón Antonio, Herrero M Dolores, Labarga Pablo, Garcia-Samaniego Javier, Soriano Vincente.   

Abstract

The Flaviviridae family comprises the genus Flavivirus, Hepacivirus and Pestivirus. These viruses are responsible for considerable human and animal disease and mortality worldwide. Flaviviruses cause a range of acute febrile illnesses along with encephalitic or haemorrhagic diseases. Chronic hepatitis C virus (HCV) infection is the most important hepacivirus human disease and remains a global health threat with nearly 200 million carriers worldwide. Current treatment consists in the use of peginterferon alfa (pegIFN) plus ribavirin (RBV) for 24 to 72 weeks, depending on HCV genotype, baseline viral load and the achievement of rapid virological response during therapy. However, current hepatitis C therapy fails to eradicate HCV in nearly half of treated patients and is hampered by relatively serious adverse events. No effective antiviral therapy is currently available for the treatment of flaviviruses or pestiviruses. Following the relative success of antiretroviral therapy against HIV infection, rapid progresses have been made in the development of specifically targeted antiviral therapies against HCV (STAT-C) and other Flaviviridae agents. Drug discovery for HCV is currently particularly exciting, since inhibitors of the HCV serine protease and the RNA-dependent RNA polymerase have recently entered the late stages of clinical development.

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Year:  2009        PMID: 19275702     DOI: 10.2174/187152609787847749

Source DB:  PubMed          Journal:  Infect Disord Drug Targets        ISSN: 1871-5265


  5 in total

Review 1.  From dengue to Zika: the wide spread of mosquito-borne arboviruses.

Authors:  Shivani Sukhralia; Mansi Verma; Shruthi Gopirajan; P S Dhanaraj; Rup Lal; Neeti Mehla; Chhaya Ravi Kant
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2018-09-28       Impact factor: 3.267

Review 2.  Experimental therapies for yellow fever.

Authors:  Justin G Julander
Journal:  Antiviral Res       Date:  2012-12-10       Impact factor: 5.970

3.  Hepatitis C virus genomic RNA dimerization is mediated via a kissing complex intermediate.

Authors:  Sumangala Shetty; Seungtaek Kim; Tetsuro Shimakami; Stanley M Lemon; Mihaela-Rita Mihailescu
Journal:  RNA       Date:  2010-04-01       Impact factor: 4.942

4.  Hepatitis C virus triggers mitochondrial fission and attenuates apoptosis to promote viral persistence.

Authors:  Seong-Jun Kim; Gulam H Syed; Mohsin Khan; Wei-Wei Chiu; Muhammad A Sohail; Robert G Gish; Aleem Siddiqui
Journal:  Proc Natl Acad Sci U S A       Date:  2014-04-14       Impact factor: 11.205

Review 5.  A review on current status of antiviral siRNA.

Authors:  Abid Qureshi; Vaqar Gani Tantray; Altaf Rehman Kirmani; Abdul Ghani Ahangar
Journal:  Rev Med Virol       Date:  2018-04-15       Impact factor: 6.989

  5 in total

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