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暴露前治疗用于预防艾滋病病毒。

The use of preexposure treatments for HIV prophylaxis.

作者信息

Majid Adrian, Redfield Robert R, Gilliam Bruce L

机构信息

Institute of Human Virology, University of Maryland School of Medicine, Baltimore, MD, USA.

出版信息

HIV AIDS (Auckl). 2012;4:17-28. doi: 10.2147/HIV.S25082. Epub 2012 Feb 3.

DOI:10.2147/HIV.S25082
PMID:22347807
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3280625/
Abstract

Infection with human immunodeficiency virus remains a global concern with a significant number of incident infections still reported worldwide. The use of prophylaxis prior to exposure to the virus to prevent infection has been a growing area of recent research. Results in nonhuman primates and clinical trials in high-risk patient populations using preexposure prophylaxis have shown promising results in terms of efficacy and safety, especially relating to oral preexposure prophylaxis. The potential use of oral antiretroviral agents traditionally used for human immunodeficiency virus treatment as prophylaxis raises interesting considerations, such as the best agents available for such a role, long-term safety in healthy individuals, and the potential development of resistance to these agents should infection occur. From a public health perspective, the cost-effectiveness of implementing this preventive strategy has not been fully defined at this point in time.

摘要

人类免疫缺陷病毒感染仍然是一个全球关注的问题,全球仍报告有大量新发感染病例。在接触病毒之前使用预防措施来预防感染一直是近期研究中一个不断发展的领域。在非人类灵长类动物身上的研究结果以及在高危患者群体中使用暴露前预防的临床试验在疗效和安全性方面都显示出了有前景的结果,特别是与口服暴露前预防有关的方面。传统上用于治疗人类免疫缺陷病毒的口服抗逆转录病毒药物作为预防药物的潜在用途引发了一些有趣的思考,例如最适合担任这一角色的药物、健康个体的长期安全性以及如果发生感染这些药物可能产生的耐药性。从公共卫生的角度来看,目前实施这一预防策略的成本效益尚未完全明确。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b49/3280625/b1ef9e8703dc/hiv-4-017f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b49/3280625/b1ef9e8703dc/hiv-4-017f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b49/3280625/b1ef9e8703dc/hiv-4-017f1.jpg

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本文引用的文献

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Once daily dolutegravir (S/GSK1349572) in combination therapy in antiretroviral-naive adults with HIV: planned interim 48 week results from SPRING-1, a dose-ranging, randomised, phase 2b trial.每日一次多替拉韦(S/GSK1349572)联合治疗方案用于初治 HIV 成人:SPRING-1 剂量范围、随机、2b 期试验的 48 周计划中期结果。
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First phase 1 double-blind, placebo-controlled, randomized rectal microbicide trial using UC781 gel with a novel index of ex vivo efficacy.第一阶段 1 期双盲、安慰剂对照、随机直肠用杀微生物剂 UC781 凝胶的临床试验,采用新型体外疗效指标。
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Bone mineral density in HIV-negative men participating in a tenofovir pre-exposure prophylaxis randomized clinical trial in San Francisco.参与旧金山替诺福韦暴露前预防随机临床试验的 HIV 阴性男性的骨密度。
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