Gordon Y J, Romanowski E, Araullo-Cruz T, De Clercq E
Eye and Ear Institute of Pittsburgh, PA 15213.
Cornea. 1992 Nov;11(6):529-33. doi: 10.1097/00003226-199211000-00008.
Currently there is no clinically effective antiviral agent for the prevention or treatment of ocular adenoviral infections. Using a paired-eye, masked design, we tested the antiviral efficacy of topical 0.1% (S)-1-(3-hydroxy-2-phosphonylmethoxypropyl)cytosine in the New Zealand rabbit ocular model after topical and intrastromal inoculation with 100 microliters (4 x 10(5) plaque-forming units per eye) of adenovirus type 5 McEwen, a clinical isolate. Prevention studies involved pretreatment (six times a day) 1 day before inoculation and continuing for 4 additional days. Compared with the control eyes, the pretreated eyes showed a significant reduction in the peak viral eye titers on days 3, 4, 5, and 7 after treatment (p < 0.03-0.005), and a reduction in the duration of viral sheeding (p < 0.02). Rebound increase in adenoviral titers was detected in five of 20 eyes (25%) after cessation of treatment, suggesting a therapeutic effect and a need for further studies to optimize the treatment regimen.
目前尚无用于预防或治疗眼部腺病毒感染的临床有效抗病毒药物。我们采用双眼配对、遮蔽设计,在新西兰兔眼模型中,于局部和基质内接种100微升(每只眼4×10⁵ 空斑形成单位)临床分离株5型腺病毒McEwen后,测试了局部应用0.1%(S)-1-(3-羟基-2-膦酰甲氧基丙基)胞嘧啶的抗病毒效果。预防研究包括在接种前1天进行预处理(每天6次)并持续额外4天。与对照眼相比,预处理眼在治疗后第3、4、5和7天的病毒眼峰值滴度显著降低(p < 0.03 - 0.005),病毒排出持续时间缩短(p < 0.02)。治疗停止后,20只眼中有5只(25%)检测到腺病毒滴度反弹升高,提示有治疗效果且需要进一步研究以优化治疗方案。