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Detection of viral DNA to evaluate outcome of antiviral treatment of patients with recurrent genital herpes.

机译:检测病毒DNA以评估复发性生殖器疱疹患者的抗病毒治疗结果。

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摘要

Culture of infectious virus, PCR amplification of viral DNA, and the appearance of genital skin lesions were used as markers to study the course of a recurrence of genital herpes in 40 patients treated with famciclovir or placebo. The highest frequency of patients with skin lesions occurred within the first 36 h following the onset of a recurrence, which also corresponded to the peak in the production of virus. While the timing of the peak in skin lesions was independent of the type of treatment, the frequency of lesions and the release of virus at the lesion site were both reduced by famciclovir treatment. Furthermore, patients receiving this antiviral agent showed a more rapid recovery time and a shorter period during which viral DNA could be detected at the lesion. PCR and then Southern blot hybridization greatly enhanced our ability to detect herpes simplex virus at the lesion site. This procedure proved to be of greater diagnostic value in assessing genital herpes than the standard culture method currently used. In addition, PCR was more sensitive in evaluating treatment effectiveness.
机译:传染性病毒的培养,病毒DNA的PCR扩增以及生殖器皮肤病变的出现被用作标记,以研究泛昔洛韦或安慰剂治疗的40例生殖器疱疹的复发过程。皮肤病变患者的最高发生频率是在复发后的最初36小时内,这也与病毒产生的峰值相对应。尽管皮肤病损高峰的时间与治疗类型无关,但泛昔洛韦治疗可减少病灶的发生频率和病灶处病毒的释放。此外,接受这种抗病毒剂的患者显示出更快的恢复时间和更短的时间,在此期间可以在病变处检测到病毒DNA。 PCR和Southern blot杂交极大地增强了我们在病变部位检测单纯疱疹病毒的能力。与目前使用的标准培养方法相比,该方法对评估生殖器疱疹具有更大的诊断价值。此外,PCR在评估治疗效果方面更为敏感。

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