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在 HIV-1 流行中口服逆转录酶抑制剂的使用演变:从治疗到预防。

Evolving uses of oral reverse transcriptase inhibitors in the HIV-1 epidemic: from treatment to prevention.

机构信息

Division of Infection and Immunity, University College, 90 Gower St, London WC1E 6BT, UK.

出版信息

Retrovirology. 2013 Jul 31;10:82. doi: 10.1186/1742-4690-10-82.

Abstract

The HIV epidemic continues unabated, with no highly effective vaccine and no cure. Each new infection has significant economic, social and human costs and prevention efforts are now as great a priority as global antiretroviral therapy (ART) scale up. Reverse transcriptase inhibitors, the first licensed class of ART, have been at the forefront of treatment and prevention of mother to child transmission over the past two decades. Now, their use in adult prevention is being extensively investigated. We describe two approaches: treatment as prevention (TasP) - the use of combination ART (2NRTI and 1NNRTI) following HIV diagnosis to limit transmission and pre-exposure prophylaxis (PrEP) -the use of single or dual oral agents prior to sexual exposure. Prevention of mother-to-child transmission using NRTI has been highly successful, though does not involve sustained use of NRTI to limit transmission. Despite theoretical and preliminary support for TasP and PrEP, data thus far indicate that adherence, retention in care and late diagnosis are the major barriers to their successful, sustained implementation. Future advances in drug technologies will be needed to overcome the issue of drug adherence, through development of drugs that involve both less frequent dosing as well as reduced toxicity, possibly through specific targeting of infected cells.

摘要

艾滋病疫情仍在蔓延,目前尚无高效疫苗,也无法治愈。每一例新的感染都会带来巨大的经济、社会和人力成本,因此预防工作与扩大全球抗逆转录病毒治疗(ART)同样重要。过去二十年来,逆转录酶抑制剂作为第一批获得许可的 ART 药物,一直是治疗和预防母婴传播的主要手段。如今,人们正在广泛研究其在成人预防中的应用。我们介绍两种方法:治疗即预防(TasP)——在 HIV 诊断后使用联合 ART(2NRTI 和 1NNRTI)来限制传播,以及暴露前预防(PrEP)——在性行为前使用单一或双重口服药物进行预防。使用 NRTI 预防母婴传播已取得了巨大成功,但这并不涉及持续使用 NRTI 来限制传播。尽管 TasP 和 PrEP 在理论和初步研究中得到支持,但迄今为止的数据表明,坚持用药、坚持接受治疗和延迟诊断是成功实施这两种方法的主要障碍。需要通过开发更频繁的剂量和减少毒性的药物来克服药物依从性的问题,这可能需要通过针对受感染细胞的特定靶向来实现。

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