The objective of this study was to evaluate the kinetics of varicella-zoster virus (VZV) loads using quantitative PCR (qPCR) in patients treated for acute retinal necrosis (ARN). Six patients (52 ؎ 13 years old) with ARN syndrome were consecutively studied. Aqueous humor (AH) was sampled from both eyes of all patients for qPCR evaluation. The patients were treated with intravenous acyclovir and intravitreal injections of antiviral drugs. The mean follow-up time was 17.6 ؎ 16.4 months. Main outcome measures were the numbers of viral genome copies in the AH, assessed using real-time qPCR with hydrolysis probe technology with a threshold of detection of 200 copies/ml. Two main portions of the viral load curves were observed for each patient: a plateau phase (27.8 ؎ 24.9 days) and a decrease in the number of viral genome copies. The mean baseline viral load was 3.4 ؋ 10 7 ؎ 4.45 ؋ 10 7 copies/ml (6 ؋ 10 6 to 1.2 ؋ 10 8 copies/ml). The viral load decreased according to a logarithmic model, with a 50% reduction obtained in 3 ؎ 0.7 days. There was a significant viral load (>102 copies/ml) at 50 days after the onset of treatment, despite antiviral drugs. qPCR use demonstrated reproducible VZV DNA kinetics with a two-phase evolution: a plateau followed by a logarithmic decrease. These data suggest that high-dosage antiviral therapy administered for the conventional 10-day duration is insufficient for most patients. This series of patients responded with a similar decrease in viral load once treatment was initiated, and the data from these patients may be used to predict the responses of future patients.
Acute retinal necrosis syndrome (ARN), one of the most serious infectious ocular diseases, is caused by herpesviruses, with varicella-zoster virus (VZV) being the most common (1, 2). Great advances have been made in the diagnosis of viral retinitis with the detection of viral DNA in intraocular fluids (vitreous and aqueous humor [AH]) and accurate quantification of viral genome copies using real-time quantitative PCR (qPCR) (3, 4).The extent of retinitis, such as anterior chamber and vitreous inflammation, vasculitis, retinal necrosis, and scarring of the involved retina, is currently monitored with physical examination. Vitreous opacities and/or cataract development, however, may preclude visualization of the posterior segment, making clinical monitoring and appraisal of the efficacy of antiviral treatment difficult. At this time, it is not known whether the kinetics of viral DNA during systemic treatment (i.e., acyclovir [5], valacyclovir [6,7], or famciclovir [6-8] and/or intravitreal therapy [9]) is similar in all patients and can be predicted once the treatment is initiated.The objective of this case series was to assess the evolution of VZV DNA loads after systemic/intravitreal antiviral treatment in ARN and to evaluate the contribution of qPCR to the monitoring of patients with VZV acute retinal necrosis.
MATERIALS AND METHODSThis retrospective study was conducted in a tertiary center with a consecutive series of s...