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MicroRNAs, Hepatitis C Virus, and HCV/HIV-1 Co-Infection: New Insights in Pathogenesis and Therapy

Journal

VIRUSES-BASEL
Volume 4, Issue 11, Pages 2485-2513

Publisher

MDPI
DOI: 10.3390/v4112485

Keywords

microRNA; miR-122; exosomes; HCV; hepatitis C virus; hepatitis; antiviral response; HIV-1; HIV-1/HCV co-infection; antagomir; therapeutics

Categories

Funding

  1. Public Health Service from the National Institute of Neurological Disorders and Stroke [NS061179, AI088423, DK089314, NS065727, AI098549]
  2. National Institute of Allergy and Infectious Disease
  3. National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
  4. Drexel University College of Medicine's Internal Funds

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MicroRNAs (miRNAs) can exert a profound effect on Hepatitis C virus (HCV) replication. The interaction of HCV with the highly liver-enriched miRNA, miR-122 represents one such unique example of viruses having evolved mechanism(s) to usurp the host miRNA machinery to support viral life cycle. Furthermore, HCV infection can also trigger changes in the cellular miRNA profile, which may ultimately contribute to the outcome of viral infection. Accumulating knowledge on HCV-host miRNA interactions has ultimately influenced the design of therapeutic interventions against chronic HCV infection. The importance of microRNA modulation in Human Immunodeficiency Virus (HIV-1) replication has been reported, albeit only in the context of HIV-1 mono-infection. The development of HCV infection is dramatically influenced during co-infection with HIV-1. Here, we review the current knowledge on miRNAs in HCV mono-infection. In addition, we discuss the potential role of some miRNAs, identified from the analyses of public data, in HCV/HIV-1 co-infection.

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