Therapeutic Silencing of MicroRNA-122 in Primates with Chronic Hepatitis C Virus Infection

Author:

Lanford Robert E.1,Hildebrandt-Eriksen Elisabeth S.2,Petri Andreas2,Persson Robert2,Lindow Morten2,Munk Martin E.2,Kauppinen Sakari23,Ørum Henrik2

Affiliation:

1. Department of Virology and Immunology and Southwest National Primate Research Center, Southwest Foundation for Biomedical Research, San Antonio, TX 78227, USA.

2. Santaris Pharma, Kogle Allé 6, DK-2970 Hørsholm, Denmark.

3. Copenhagen Institute of Technology, Aalborg University, Lautrupvang 15, DK-2750 Ballerup, Denmark.

Abstract

Anti-MicroRNA Antiviral MicroRNAs (miRNAs) are small noncoding RNAs found in eukaryotes and viruses. They are critical regulators of a wide range of cellular processes. The highly conserved miRNA miR-122 is required for infection by hepatitis C virus (HCV), a leading cause of liver disease in humans. Present HCV treatment regimes can have serious side effects and are effective in only 50% of cases. In order to try to tackle HCV infection, Lanford et al. (p. 198 , published online 3 December) targeted miR-122 using a complementary locked nucleic acid (LNA) oligonucleotide. Treatment of chimpanzees infected by HCV with the LNA antagonist resulted in a long-term reduction of disease symptoms without the concomitant appearance of resistant strains of the virus.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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