首页> 美国卫生研究院文献>The British Journal of Ophthalmology >Detection of herpes simplex virus type 1 2 and varicella zoster virus DNA in recipient corneal buttons
【2h】

Detection of herpes simplex virus type 1 2 and varicella zoster virus DNA in recipient corneal buttons

机译:检测受体角膜纽扣中的1型2型单纯疱疹病毒和水痘带状疱疹病毒DNA

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

AIM—To study the value of polymerase chain reaction (PCR) analysis, to detect viral DNA in recipient corneal buttons taken at the time of penetrating keratoplasty (PKP) in patients with an initial diagnosis of herpetic stromal keratitis (HSK). Since HSK has a tendency to recur, an accurate diagnosis of previous HSK could be the reason to start antiviral treatment immediately, thereby possibly decreasing the number of graft failures due to recurrent herpetic keratitis.
METHODS—Recipient corneal buttons and aqueous humour (AH) samples were obtained at the time of PKP from HSK patients (n=31) and from other patients (n=78). Eye bank corneas were also used (n=23). Herpes simplex virus type 1 (HSV-1), type 2 (HSV-2), and varicella zoster virus (VZV) infection were assessed by PCR and antibody detection.
RESULTS—The clinical diagnosis HSK could be confirmed by PCR for HSV-1 in 10/31 (32%). In these corneal buttons HSV-2 DNA was detected in 1/31 (3%) and VZV DNA in 6/31 (19%). Intraocular anti-HSV antibody production was detected in 9/28 AH samples tested (32%). In the other patient derived corneas HSV-1 DNA was detected in 13/78 (17%), including eight failed corneal grafts without clinically obvious herpetic keratitis in the medical history. In clear eye bank corneas HSV-1 was detected in 1/23 (4%).
CONCLUSIONS—PCR of HSV-1 on corneal buttons can be a useful diagnostic tool in addition to detection of intraocular anti-HSV antibody production. Furthermore, the results were suggestive for the involvement of corneal HSV infection during allograft failure of corneas without previous clinical characteristic signs of herpetic keratitis.

机译:目的:研究聚合酶链反应(PCR)分析的价值,检测初次诊断为疱疹性间质性角膜炎(HSK)的患者在穿透性角膜移植术(PKP)时采集的受体角膜纽扣中的病毒DNA。由于HSK有复发的趋势,因此对先前HSK的准确诊断可能是立即开始抗病毒治疗的原因,从而可能减少由于复发性疱疹性角膜炎而引起的移植失败的次数。
方法-收件人角膜纽扣和房水(AH)样本是在PKP时从HSK患者(n = 31)和其他患者(n = 78)获得的。还使用了眼库角膜(n = 23)。通过PCR和抗体检测评估了1型单纯疱疹病毒(HSV-1),2型(HSV-2)和水痘带状疱疹病毒(VZV)的感染。
结果—PCR可确诊HSK的临床诊断HSV-1在10/31(32%)。在这些角膜纽扣中,在1/31(3%)中检测到HSV-2 DNA,在6/31(19%)中检测到VZV DNA。在测试的9/28个AH样品中检测到了眼内抗HSV抗体的产生(32%)。在另一位患者中,在病史中检出的角膜HSV-1 DNA占13/78(17%),包括8例角膜移植失败,而没有临床上明显的疱疹性角膜炎。在透明眼库中,在1/23(4%)的角膜中检测到HSV-1。
结论—除了检测眼内抗HSV抗体的产生,在角膜纽扣上进行HSV-1 PCR还可作为一种有用的诊断工具。此外,该结果提示在没有先前的疱疹性角膜炎临床特征性体征的角膜同种异体移植失败期间,角膜HSV感染的发生。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号