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Antimicrobial Agents and Chemotherapy, July 2001, p. 2044-2053, Vol. 45, No. 7
Department of Ophthalmology, LSU Eye Center,
Louisiana State University Health Sciences Center, New Orleans,
Louisiana 70112-2234,1 and Department of
Molecular Virology and Host Defense, SmithKline Beecham
Pharmaceuticals, Collegeville, Pennsylvania
19426-09892
Received 14 September 2000/Returned for modification 22 December
2000/Accepted 25 April 2001
Famciclovir (FCV) is efficacious in the treatment of acute herpes
zoster and recurrent genital infections but has not been used to treat
ocular herpes simplex virus (HSV) infections. We evaluated the efficacy
of orally administered FCV in treating HSV-1 epithelial keratitis and
determined its effects on the establishment of latency and subsequent
reactivation. Rabbits were inoculated with HSV-1 strain 17 syn+ and
treated twice daily with increasing concentrations of FCV (60 to 500 mg/kg of body weight). This resulted in a significant, dose-dependent
improvement in keratitis scores, as well as prolonged survival.
Regardless of the dose of drug used, all groups exhibited the high
rates of spontaneous and induced reactivation characteristic of 17syn+.
The efficacy of 250 mg of FCV per kg was also compared to topical
treatment with 1% trifluorothymidine (TFT). Although TFT treatment was
more effective at reducing eye disease, FCV-treated rabbits had a
better survival rate. Real-time quantitative PCR analysis of rabbit
trigeminal ganglia (TG) demonstrated that FCV significantly reduced the
HSV-1 copy number compared to that after treatment with TFT or the
placebo but not in a dose-dependent manner. In summary, oral FCV
treatment significantly reduces the severity of corneal lesions,
reduces the number of HSV-1 genomes in the TG, improves survival, and
therefore may be beneficial in reducing the morbidity of HSV keratitis
in the clinic.
0066-4804/01/$04.00+0 DOI: 10.1128/AAC.45.7.2044-2053.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Effect of Famciclovir on Herpes Simplex Virus Type
1 Corneal Disease and Establishment of Latency in Rabbits
*
Corresponding author. Mailing address: LSU Eye Center,
LSU Health Sciences Center, 2020 Gravier St., Suite B, New Orleans, LA
70112. Phone: (504) 412-1200, ext. 1328. Fax: (504) 412-1315. E-mail:
jlouts{at}lsuhsc.edu.
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