sirna for influenza therapy可以阻止流感药物治疗.pdfVIP

Viruses 2010, 2, 1448-1457; doi:10.3390/v2071448 OPEN ACCESS viruses ISSN 1999-4915 /journal/viruses Review siRNA for Influenza Therapy Sailen Barik Department of Biochemistry and Molecular Biology, University of South Alabama, College of Medicine, MSB 2370, 307 University Boulevard, Mobile, AL 36688-0002, USA; E-Mail: sbarik@; Tel.: +1-251-460-6860; Fax: +1-251-460-6850 Received: 1 June 2010; in revised form: 5 July 2010 / Accepted: 7 July 2010 / Published: 9 July 2010 Abstract: Influenza virus is one of the most prevalent and ancient infections in humans. About a fifth of worlds population is infected by influenza virus annually, leading to high morbidity and mortality, particularly in infants, the elderly and the immunocompromised. In the US alone, influenza outbreaks lead to roughly 30,000 deaths each year. Current vaccines and anti-influenza drugs are of limited use due to high mutation rate of the virus and side effects. In recent years, RNA interference, triggered by synthetic short interfering RNA (siRNA), has rapidly evolved as a potent antiviral regimen. Properly designed siRNAs have been shown to function as potent inhibitors of influenza virus replication. The siRNAs outperform traditional small molecule antivirals in a number of areas, such as ease of design, modest cost, and fast turnaround. Although specificity and tissue delivery remain major bottlenecks in the clinical applications