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在一项多大陆临床试验中,阿昔洛韦抑制单纯疱疹病毒 2 型的临床和病毒学疗效。

Clinical and virologic efficacy of herpes simplex virus type 2 suppression by acyclovir in a multicontinent clinical trial.

机构信息

HIV Research Section, San Francisco Department of Public Health, San Francisco, CA 94102, USA.

出版信息

J Infect Dis. 2010 Apr 15;201(8):1164-8. doi: 10.1086/651381.

Abstract

Acyclovir suppressive therapy (400 mg twice daily) reduces herpes simplex virus (HSV) type 2-associated genital ulcer disease and lesional HSV shedding. In an international trial of acyclovir for suppression of HSV type 2 to prevent human immunodeficiency virus (HIV) acquisition (HIV Prevention Trials Network 039), acyclovir had a smaller effect on the frequency of genital ulcer disease as well as a smaller effect on the frequency and quantity of lesional HSV DNA in African women and Peruvian men, compared with its effects in men in the United States. The observed regional variation in the clinical and virologic efficacy of acyclovir for HSV suppression warrants further evaluation of determinants of responses to acyclovir. (ClinicalTrials.gov identifier: NCT00076232.).

摘要

阿昔洛韦抑制疗法(每日两次,每次 400 毫克)可减少单纯疱疹病毒(HSV)2 型相关的生殖器溃疡病和病变部位 HSV 脱落。在一项国际阿昔洛韦抑制 HSV2 以预防人类免疫缺陷病毒(HIV)感染的试验(HIV 预防试验网络 039)中,与美国男性相比,阿昔洛韦对生殖器溃疡病的发病频率以及对病变部位 HSV DNA 的频率和数量的影响较小,在非洲女性和秘鲁男性中。阿昔洛韦抑制 HSV 的临床和病毒学疗效的观察到的区域差异需要进一步评估对阿昔洛韦反应的决定因素。(临床试验.gov 标识符:NCT00076232。)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08a3/2856478/883348cb63e0/nihms192068f1.jpg

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