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Inhibition of hepatitis C virus in chimeric mice by sshRNAs: Sequence analysis of surviving virus shows added selective pressure of combination therapy
3rd International Conference on Gastroenterology & Urology
It was previously shown that a cocktail of two short synthetic shRNAs (sshRNAs) targeting the internal ribosome entry
site of hepatitis C virus (HCV) formulated with lipid nanoparticles was able to suppress viral replication in chimeric mice
infected with HCV GT1a by up to 2.5 log10. Viral load remained about 1 log10 below pre-treatment levels 21 days after the
end of dosing. HCV viral RNA amplified from serum of treated mice after the 21-d follow-up period was sequenced. Viral
RNA from the HCV sshRNA-treated groups was altered in sequences complementary to the sshRNAs and nowhere else in
the sequenced region, while the viruses from the control group that received an irrelevant sshRNA had no mutations in that
region. The ability of the most commonly-selected mutations to confer resistance to the sshRNAs was confirmed in vitro
by introducing those mutations into HCV-luciferase reporters. The most frequent mutations selected by sshRNA treatment
within the sshRNA target sequence were at the most polymorphic residues as identified from an analysis of available clinical
isolates. These results demonstrate a direct antiviral activity with effective HCV suppression, and confirm an RNAi mechanism
of action. It is concluded that either a potent sshRNA against a highly conserved HCV target sequence or a combination
of 2 sshRNAs against two different target regions could be effective against HCV infection when combined with antiviral
agents having different mechanism(s) of action, but a cocktail comprising more than two sshRNAs would be required in any
treatment relying on sshRNAs alone.
Biography
Brian H Johnston is Founder and CEO of SomaGenics, which invents and develops RNA-based therapeutics and diagnostic tools. He holds a BA in Chemistry from
Pomona College, a PhD in Biophysical Chemistry from UC Berkeley, and performed Postdoctoral research at UC San Francisco and MIT. He subsequently moved
to SRI International, where he was a founding Director of the Nucleic Acids Program before starting SomaGenics. He is author of some 56 research publications
and reviews and has been a Principal Investigator or Co-investigator of research grants totaling $20 million. He has held faculty appointments at MIT, Stanford,
and the University of Paris.
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