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带状疱疹性眼炎后人类眼中水痘带状疱疹病毒DNA和病毒抗原的检测

Detection of varicella zoster virus DNA and viral antigen in human eyes after herpes zoster ophthalmicus.

作者信息

Wenkel H, Rummelt V, Fleckenstein B, Naumann G O

机构信息

Department of Ophthalmology, University of Erlangen-Nürnberg, Germany.

出版信息

Ophthalmology. 1998 Jul;105(7):1323-30. doi: 10.1016/S0161-6420(98)97042-7.

Abstract

OBJECTIVE

The purpose of the study was to identify varicella zoster virus (VZV) DNA and viral antigen in human eyes at various intervals after clinical onset of herpes zoster ophthalmicus (HZO).

DESIGN

A retrospective case series.

PARTICIPANTS

There were 9 eyes and 4 corneal buttons surgically obtained from 13 patients with HZO at the University Eye Hospital of Erlangen-Nürnberg between 1984 and 1994. Specimens were examined at different timepoints after clinical onset of HZO (range, 1 day-19 years; median, 36 months).

METHODS

Histopathologic evaluation was performed on formalin-fixed and paraffin-embedded tissue by routine histology, immunohistochemistry (5-B-7 murine monoclonal antibody to VZV; peroxidase-antiperoxidase method), and DNA-in situ hybridization (35S deoxyadenosine triphosphate-labeled HindIII fragments [A and C] of VZV).

RESULTS

Typical histopathologic changes associated with HZO were identified: vascularization of the corneal stroma (11 of 13), granulomatous reaction to Descemet's membrane (8 of 13), fusiform-shaped ciliary scarring (5 of 9), optic neuritis (4 of 9), and perineuritis (8 of 9) and perivasculitis (8 of 9) of the long posterior ciliary nerves and arteries. VZV antigen was detected in two patients with acute infection 1 and 7 days after onset of HZO, respectively. VZV-DNA was identified in seven patients up to 10 years after onset of HZO in corneal epithelial cells (2 of 13), corneal stroma (5 of 13), inflammatory infiltrate of the anterior chamber (1 of 9), episclera (2 of 9), posterior ciliary nerves (1 of 9) and arteries (5 of 9), optic nerve (5 of 9), and adjacent leptomeninges (2 of 9).

CONCLUSION

Persistence of viral genomes, most likely accompanied by gene expression or slow viral replication, appears to be responsible for the often smoldering panophthalmitis and the chronic recurrent keratouveitis in patients with HZO. Localization of viral DNA in vascular structures suggests a role for vasculitis in the pathogenesis of some ocular findings associated with HZO.

摘要

目的

本研究的目的是在眼部带状疱疹(HZO)临床发病后的不同时间间隔,鉴定人眼内的水痘带状疱疹病毒(VZV)DNA和病毒抗原。

设计

一项回顾性病例系列研究。

参与者

1984年至1994年间,在埃尔朗根 - 纽伦堡大学眼科医院,从13例HZO患者身上手术获取了9只眼和4个角膜组织块。在HZO临床发病后的不同时间点(范围为1天至19年;中位数为36个月)对标本进行检查。

方法

对福尔马林固定、石蜡包埋的组织进行组织病理学评估,采用常规组织学、免疫组织化学(抗VZV的5 - B - 7鼠单克隆抗体;过氧化物酶 - 抗过氧化物酶法)和DNA原位杂交(VZV的35S脱氧腺苷三磷酸标记的HindIII片段[A和C])。

结果

鉴定出与HZO相关的典型组织病理学变化:角膜基质血管化(13例中的11例)、对Descemet膜的肉芽肿反应(13例中的8例)、梭形睫状瘢痕形成(9例中的5例)、视神经炎(9例中的4例)以及长睫状后神经和动脉的神经炎(9例中的8例)和血管周围炎(9例中的8例)。分别在HZO发病后1天和7天的2例急性感染患者中检测到VZV抗原。在HZO发病后长达10年的7例患者中,在角膜上皮细胞(13例中的2例)、角膜基质(13例中的5例)、前房炎性浸润(9例中的1例)、巩膜表层(9例中的2例)、睫状后神经(9例中的1例)和动脉(9例中的5例)、视神经(9例中的5例)以及相邻软脑膜(9例中的2例)中鉴定出VZV - DNA。

结论

病毒基因组的持续存在,很可能伴随着基因表达或缓慢的病毒复制,似乎是HZO患者中经常隐匿性全眼球炎和慢性复发性角膜葡萄膜炎的原因。病毒DNA在血管结构中的定位表明血管炎在与HZO相关的一些眼部病变发病机制中起作用。

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