University of Connecticut School of Pharmacy, Storrs, Connecticut, USA.
Ther Clin Risk Manag. 2010 Oct 5;6:431-41. doi: 10.2147/TCRM.S4207.
The worldwide emergence of multidrug-resistant human immunodeficiency virus (HIV)-1 strains has the driven the development of new antiretroviral (ARV) agents. Over the past 5 years, HIV-entry and integrase inhibitor ARVs, as well as improved non-nucleoside reverse transcriptase inhibitors (NRTIs) and protease inhibitors (PIs), have become available for treatment. It is important to assess how these new ARVs might be most judiciously used, paying close attention to viral susceptibility patterns, pharmacodynamic parameters, and the likelihood that patients will adhere to their therapy. Herein we review published material in Medline, EMBASE, and ISI for each antiretroviral agent/classes currently approved and summarize the available data on their efficacy, safety, and pharmacologic parameters. We focus on the role of tipranavir, a recently approved nonpeptidic PI, for treating HIV-infected children, adolescents, and adults with a history of multidrug-resistant HIV.
全球出现的多种抗药性人类免疫缺陷病毒(HIV)-1 株系促使新的抗逆转录病毒(ARV)药物的研发。在过去的 5 年中,HIV 进入抑制剂和整合酶抑制剂 ARV,以及改良的非核苷类逆转录酶抑制剂(NRTIs)和蛋白酶抑制剂(PIs)已经可以用于治疗。评估这些新的 ARV 如何被最合理地使用非常重要,需要密切关注病毒敏感性模式、药效学参数以及患者遵守治疗的可能性。本文回顾了 Medline、EMBASE 和 ISI 中已发表的关于目前批准的每种抗逆转录病毒药物/类别的资料,并总结了有关其疗效、安全性和药物参数的现有数据。我们重点关注最近批准的非肽类蛋白酶抑制剂替拉那韦在治疗有多种抗药性 HIV 史的 HIV 感染儿童、青少年和成人中的作用。