Zamansky G B, Lee B P, Chang R K, Hendricks K, Ryan W J, Leibowitz H M
Invest Ophthalmol Vis Sci. 1985 Jun;26(6):873-6.
The authors have developed an objective method for quantitation of herpes simplex virus in the corneal epithelium of rabbits. At appropriate times postinfection, full-thickness rabbit corneas were removed by trephination and subjected to one cycle of freezing and thawing. The corneal epithelium was then disrupted by sonication. The amount of infectious virus recovered from sonicated specimens was determined by an in vitro plaque assay, providing a measure of the quantity of virus present during the acute stage of herpetic keratitis. Using this technique, the authors found that the mean virus titer was reduced from 1.5 X 10(5) plaque forming units (pfu) per cornea in control rabbits to less than 200 pfu per cornea in rabbits treated topically for 2 days with 1% trifluridine. In contrast, instillation of 1% prednisolone acetate resulted in the persistence of higher levels of virus (275 pfu) than those observed in control rabbits (3 pfu) 4 days after the cessation of therapy.
作者们开发了一种客观方法,用于定量兔角膜上皮中的单纯疱疹病毒。在感染后的适当时间,通过环钻术取下全层兔角膜,并进行一个冻融循环。然后通过超声处理破坏角膜上皮。通过体外空斑试验确定从经超声处理的标本中回收的感染性病毒量,从而提供疱疹性角膜炎急性期存在的病毒量的一种度量。使用该技术,作者们发现,对照兔每只角膜的平均病毒滴度从1.5×10⁵空斑形成单位(pfu)降至用1%三氟胸苷局部治疗2天的兔每只角膜低于200 pfu。相比之下,在停止治疗4天后,滴注1%醋酸泼尼松龙导致病毒水平(275 pfu)持续高于对照兔(3 pfu)中观察到的水平。