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Antimicrobial Agents and Chemotherapy, July 2001, p. 2044-2053, Vol. 45, No. 7
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

Jeannette M. Loutsch,1,* Bruno Sainz Jr.,1 Mary E. Marquart,1 Xiaodong Zheng,1 Prabakaran Kesavan,2 Shiro Higaki,1 James M. Hill,1 and Ruth Tal-Singer2

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.


* 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.


Antimicrobial Agents and Chemotherapy, July 2001, p. 2044-2053, Vol. 45, No. 7
0066-4804/01/$04.00+0   DOI: 10.1128/AAC.45.7.2044-2053.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Sainz, B. Jr, Halford, W. P. (2002). Alpha/Beta Interferon and Gamma Interferon Synergize To Inhibit the Replication of Herpes Simplex Virus Type 1. J. Virol. 76: 11541-11550 [Abstract] [Full Text]