Abstract | PURPOSE: The aim of this study was to evaluate the effect of BAY 57-1293, a helicase- primase inhibitor, on herpes simplex virus type 1 (HSV-1) reactivation in mice and its efficacy on established disease in rabbits. METHODS: BALB/c mice latent for McKrae-strain HSV-1 were reactivated via heat stress, treated with BAY 57-1293, and their corneas were swabbed for virus or the trigeminal ganglia (TG) obtained for quantification of viral DNA. New Zealand white rabbits were infected and treated topically or orally in comparison with trifluridine or valacyclovir. RESULTS: Oral BAY 57-1293 suppressed reactivation in HSV-1-infected mice and reduced the viral load in TG up to four orders of magnitude. In the rabbits, the therapeutic efficacies of topical BAY 57-1293 and trifluridine were similar. Once-daily oral BAY 57-1293 was significantly more effective than valacyclovir and as effective as twice a day topical trifluridine. CONCLUSIONS:
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Authors | Herbert E Kaufman, Emily D Varnell, Bryan M Gebhardt, Hilary W Thompson, Ephraim Atwal, Helga Rübsamen-Waigmann, Gerald Kleymann |
Journal | Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics
(J Ocul Pharmacol Ther)
Vol. 24
Issue 1
Pg. 34-42
(Feb 2008)
ISSN: 1080-7683 [Print] United States |
PMID | 18201137
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
- DNA, Viral
- Enzyme Inhibitors
- Pyridines
- Sulfonamides
- Thiazoles
- Viral Proteins
- pritelivir
- DNA Primase
- helicase-primase, Human herpesvirus 1
- DNA Helicases
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Topics |
- Animals
- DNA Helicases
(antagonists & inhibitors)
- DNA Primase
(antagonists & inhibitors)
- DNA, Viral
(chemistry)
- Enzyme Inhibitors
(therapeutic use)
- Female
- Heat Stress Disorders
(virology)
- Herpesvirus 1, Human
- Keratitis, Herpetic
(drug therapy)
- Mice
- Mice, Inbred BALB C
- Pyridines
(therapeutic use)
- Rabbits
- Sulfonamides
- Tears
(virology)
- Thiazoles
(therapeutic use)
- Trigeminal Ganglion
(virology)
- Viral Proteins
(antagonists & inhibitors)
- Virus Shedding
(drug effects)
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