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抗逆转录病毒药物的发现与开发。

The discovery and development of antiretroviral agents.

作者信息

Lange Joep M A, Ananworanich Jintanat

机构信息

Department of Global Health, Academic Medical Center, University of Amsterdam, Amsterdam Institute for Global Health and Development, Amsterdam, the Netherlands.

出版信息

Antivir Ther. 2014;19 Suppl 3:5-14. doi: 10.3851/IMP2896. Epub 2014 Oct 13.

Abstract

Since the discovery of HIV as the causative agent of AIDS in 1983/1984, remarkable progress has been made in finding antiretroviral drugs (ARVs) that are effective against it. A major breakthrough occurred in 1996 when it was found that triple drug therapy (HAART) could durably suppress viral replication to minimal levels. It was then widely felt, however, that HAART was too expensive and complex for low- and middle-income countries, and so, with the exception of a few of these countries, such as Brazil, a massive scale-up did not begin until the WHO launched its '3 by 5' initiative and sizeable funding mechanisms, such as the Global Fund to Fight AIDS, TB and Malaria and the US President's Emergency Plan for AIDS Relief (PEPFAR), came into existence. A pivotal enabler of the scale-up was a steady lowering of drug prices through entry of generic antiretrovirals, competition between generic manufacturers and the making of volume commitments. The WHO Prequalification of Medicines Programme and the Expedited Review Provision of the US Food and Drug Administration have been important for the assurance of quality standards. Antiretroviral drug development by research-based pharmaceutical companies continues, with several important innovative products, such as long-acting agents, in the pipeline.

摘要

自1983年/1984年发现人类免疫缺陷病毒(HIV)是获得性免疫综合征(AIDS,艾滋病)的病原体以来,在寻找有效的抗逆转录病毒药物(ARV)方面取得了显著进展。1996年取得了一项重大突破,当时发现三联药物疗法(高效抗逆转录病毒疗法,HAART)能够将病毒复制持久抑制到最低水平。然而,当时人们普遍认为,HAART对于低收入和中等收入国家来说过于昂贵和复杂,因此,除了少数几个国家(如巴西)外,直到世界卫生组织发起其“3 by 5”倡议以及诸如全球抗击艾滋病、结核病和疟疾基金以及美国总统艾滋病紧急救援计划(PEPFAR)等大量资金机制出现后,大规模推广才开始。推广的一个关键推动因素是通过仿制药抗逆转录病毒药物的进入、仿制药制造商之间的竞争以及做出批量承诺,使药品价格稳步下降。世界卫生组织药品预认证计划和美国食品药品监督管理局的快速审查规定对于确保质量标准至关重要。以研究为基础的制药公司的抗逆转录病毒药物研发仍在继续,有几种重要的创新产品(如长效制剂)正在研发中。

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