Emerging resistance profiles of newly approved antiretroviral drugs.

Eric S Daar
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Abstract

The antiretroviral treatment goal in highly treatment-experienced patients is now suppression of viral replication to undetectable levels, a goal that can be achieved by strategic use of combinations that include newer antiretroviral drugs. Newer drugs in established classes that improve virologic response when added to optimized background therapy include the protease inhibitors darunavir and tipranavir and the second-generation nonnucleoside analogue reverse transcriptase inhibitor etravirine. New drugs from new classes that have proved active in treatment-experienced patients include the chemokine coreceptor 5 (CCR5) antagonist maraviroc and the integrase strand-transfer inhibitor raltegravir. Knowledge of the resistance patterns and predictors of response with these new agents and careful selection of background therapy are crucial to maximizing virologic response and preventing emergence of resistance. This article summarizes a presentation on emerging resistance profiles of newer antiretroviral drugs made by Eric S. Daar, MD, at an International AIDS Society-USA Continuing Medical Education course in Los Angeles in March 2008. The original presentation is available as a Webcast at www.iasusa.org.

新批准的抗逆转录病毒药物的耐药概况。
在治疗经验丰富的患者中,抗逆转录病毒治疗的目标现在是将病毒复制抑制到无法检测的水平,这一目标可以通过战略性地使用包括较新的抗逆转录病毒药物的组合来实现。在已建立的药物类别中,当添加到优化的背景治疗中时,可以改善病毒学反应的新药包括蛋白酶抑制剂darunavir和tipranavir以及第二代非核苷类似物逆转录酶抑制剂etravirine。来自新类别的新药已被证明对治疗经验丰富的患者有效,包括趋化因子辅助受体5 (CCR5)拮抗剂马拉维洛克和整合酶链转移抑制剂雷替格拉韦。了解这些新药物的耐药模式和反应预测因素以及仔细选择背景治疗对于最大限度地提高病毒学反应和防止耐药性的出现至关重要。本文总结了Eric S. Daar医学博士2008年3月在洛杉矶举行的美国国际艾滋病协会继续医学教育课程上关于新出现的抗逆转录病毒药物耐药概况的报告。原始演示可以在www.iasusa.org上以网络广播的形式获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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