| Autor: |
Bryant, Martin L., Bridges, Edward G., Placidi, Laurent, Faraj, Abdesslem, Loi, Anna-Giulia, Pierra, Claire, Dukhan, David, Gosselin, Gilles, Imbach, Jean-Louis, Hernandez, Brenda, Juodawlkis, Amy, Tennant, Bud, Korba, Brent, Cote, Paul, Marion, Pat, Cretton-Scott, Erika, Schinazi, Raymond F., Sommadossi, Jean-Pierre |
| Zdroj: |
Antimicrobial Agents and Chemotherapy; January 2001, Vol. 45 Issue: 1 p229-235, 7p |
| Abstrakt: |
ABSTRACTA unique series of simple “unnatural” nucleosides has been discovered to inhibit hepatitis B virus (HBV) replication. Through structure-activity analysis it was found that the 3′-OH group of the β-l-2′-deoxyribose of the β-l-2′-deoxynucleoside confers specific antihepadnavirus activity. The unsubstituted nucleosides β-l-2′-deoxycytidine, β-l-thymidine, and β-l-2′-deoxyadenosine had the most potent, selective, and specific antiviral activity against HBV replication. Human DNA polymerases (α, β, and γ) and mitochondrial function were not affected. In the woodchuck model of chronic HBV infection, viral load was reduced by as much as 108genome equivalents/ml of serum and there was no drug-related toxicity. In addition, the decline in woodchuck hepatitis virus surface antigen paralleled the decrease in viral load. These investigational drugs, used alone or in combination, are expected to offer new therapeutic options for patients with chronic HBV infection. |
| Databáze: |
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