| Literature DB >> 27032991 |
Katrin Schaar1, Carsten Röger2, Tanja Pozzuto1, Jens Kurreck1, Sandra Pinkert1, Henry Fechner1.
Abstract
Adenovirus (Ad) infections are usually mild and self-limiting, but severe systemic infections and fatal diseases can occur, especially in immunosuppressed patients. Anti-adenoviral pharmacotherapy has been proven to inhibit Ad infection, but its efficiency is limited. This review addresses biological antiviral agents as a new class of therapeutics for treatment of Ad infections. One group of agents is composed of short double-stranded RNA molecules that have been developed to inhibit Ad receptor and Ad protein expression. The second group of agents includes soluble virus receptor traps which inhibit Ad uptake into cells. Anti-Ad-adoptive T-cell therapy constitutes a third approach. We also outline how the combination of biological antiviral agents and combinations of these agents with the classical antiviral drugs can increase therapeutic efficiency in anti-adenoviral treatments.Entities:
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Year: 2016 PMID: 27032991 DOI: 10.3851/IMP3047
Source DB: PubMed Journal: Antivir Ther ISSN: 1359-6535