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Cytomegalovirus and the eye.巨细胞病毒与眼睛。
Eye (Lond). 2012 Feb;26(2):237-40. doi: 10.1038/eye.2011.327. Epub 2011 Dec 16.
2
The treatment of HSV1 ocular infections using quantitative real-time PCR results.使用实时荧光定量 PCR 结果治疗 HSV1 眼部感染。
Acta Ophthalmol. 2012 Aug;90(5):456-60. doi: 10.1111/j.1755-3768.2010.01933.x. Epub 2010 Jun 10.
3
Effect of high versus low oral doses of valacyclovir on herpes simplex virus-1 DNA shedding into tears of latently infected rabbits.高剂量与低剂量伐昔洛韦对潜伏感染兔单纯疱疹病毒 1 型 DNA 排入泪液的影响。
Invest Ophthalmol Vis Sci. 2010 Sep;51(9):4703-6. doi: 10.1167/iovs.09-4884. Epub 2010 Apr 14.
4
Treatment of acute retinal necrosis.急性视网膜坏死的治疗。
Ophthalmology. 2010 Apr;117(4):818-24. doi: 10.1016/j.ophtha.2009.09.001. Epub 2010 Jan 15.
5
Long-term follow-up of acute retinal necrosis.急性视网膜坏死的长期随访。
Retina. 2010 May;30(5):795-800. doi: 10.1097/IAE.0b013e3181c7013c.
6
Acute retinal necrosis: the effects of intravitreal foscarnet and virus type on outcome.急性视网膜坏死:玻璃体内膦甲酸和病毒类型对预后的影响。
Ophthalmology. 2010 Mar;117(3):556-60. doi: 10.1016/j.ophtha.2009.08.003. Epub 2009 Dec 23.
7
A double-blind placebo-controlled study to evaluate valacyclovir alone and with aspirin for asymptomatic HSV-1 DNA shedding in human tears and saliva.一项双盲安慰剂对照研究,旨在评估单用伐昔洛韦以及伐昔洛韦与阿司匹林联用对人泪液和唾液中无症状单纯疱疹病毒1型DNA脱落的影响。
Invest Ophthalmol Vis Sci. 2009 Dec;50(12):5601-8. doi: 10.1167/iovs.09-3729. Epub 2009 Jul 15.
8
Acute retinal necrosis: clinical features, early vitrectomy, and outcomes.急性视网膜坏死:临床特征、早期玻璃体切除术及预后
Ophthalmology. 2009 Oct;116(10):1971-5.e2. doi: 10.1016/j.ophtha.2009.03.029. Epub 2009 Jul 9.
9
Interlaboratory comparison of cytomegalovirus viral load assays.巨细胞病毒病毒载量检测的实验室间比对
Am J Transplant. 2009 Feb;9(2):258-68. doi: 10.1111/j.1600-6143.2008.02513.x.
10
Therapy for acute retinal necrosis.急性视网膜坏死的治疗
Semin Ophthalmol. 2008 Jul-Aug;23(4):285-90. doi: 10.1080/08820530802111192.

应用实时荧光定量 PCR 检测带状疱疹病毒急性视网膜坏死患者水样液中病毒 DNA 的时间分布。

Time profile of viral DNA in aqueous humor samples of patients treated for varicella-zoster virus acute retinal necrosis by use of quantitative real-time PCR.

机构信息

Department of Ophthalmology, CHU de Grenoble, University Hospital/Université Joseph Fourier-Grenoble 1, Grenoble, France.

出版信息

J Clin Microbiol. 2013 Jul;51(7):2160-6. doi: 10.1128/JCM.00294-13. Epub 2013 May 1.

DOI:10.1128/JCM.00294-13
PMID:23637296
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3697691/
Abstract

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.

摘要

本研究旨在通过定量 PCR(qPCR)评估急性视网膜坏死(ARN)患者治疗中水痘带状疱疹病毒(VZV)载量的动力学。连续研究了 6 名(52±13 岁)ARN 综合征患者。对所有患者的双眼房水进行 qPCR 评估取样。患者接受静脉阿昔洛韦和抗病毒药物玻璃体内注射治疗。平均随访时间为 17.6±16.4 个月。主要观察指标为使用实时 qPCR 水解探针技术评估房水中的病毒基因组拷贝数,检测下限为 200 拷贝/ml。每个患者的病毒载量曲线有两个主要部分:一个平台期(27.8±24.9 天)和病毒基因组拷贝数减少。平均基线病毒载量为 3.4×10(7)±4.45×10(7)拷贝/ml(6×10(6)至 1.2×10(8)拷贝/ml)。病毒载量根据对数模型下降,在 3±0.7 天内降低 50%。尽管使用了抗病毒药物,但在治疗开始后 50 天仍存在高病毒载量(>102 拷贝/ml)。qPCR 检测显示 VZV DNA 具有双相演变的可重复动力学:平台期后呈对数下降。这些数据表明,对于大多数患者,传统的 10 天高剂量抗病毒治疗是不够的。一旦开始治疗,这一系列患者的病毒载量均呈相似下降,这些患者的数据可用于预测未来患者的反应。