Pavlos Rebecca, Phillips Elizabeth J
Institute for Immunology and Infectious Diseases, Murdoch University, Murdoch, Western Australia, Australia.
Pharmgenomics Pers Med. 2012;5:1-17. doi: 10.2147/PGPM.S15303. Epub 2011 Dec 29.
Antiretroviral therapy (ART) has evolved considerably over the last three decades. From the early days of monotherapy with high toxicities and pill burdens, through to larger pill burdens and more potent combination therapies, and finally, from 2005 and beyond where we now have the choice of low pill burdens and once-daily therapies. More convenient and less toxic regimens are also becoming available, even in resource-poor settings. An understanding of the individual variation in response to ART, both efficacy and toxicity, has evolved over this time. The strong association of the major histocompatibility class I allele HLA-B*5701 and abacavir hypersensitivity, and its translation and use in routine HIV clinical practice as a predictive marker with 100% negative predictive value, has been a success story and a notable example of the challenges and triumphs in bringing pharmacogenetics to the clinic. In real clinical practice, however, it is going to be the exception rather than the rule that individual biomarkers will definitively guide patient therapy. The need for individualized approaches to ART has been further increased by the importance of non-AIDS comorbidities in HIV clinical practice. In the future, the ideal utilization of the individualized approach to ART will likely consist of a combined approach using a combination of knowledge of drug, virus, and host (pharmacogenetic and pharmacoecologic [factors in the individual's environment that may be dynamic over time]) information to guide the truly personalized prescription. This review will focus on our knowledge of the pharmacogenetics of the efficacy and toxicity of currently available antiretroviral agents and the current and potential utility of such information and approaches in present and future HIV clinical care.
在过去三十年中,抗逆转录病毒疗法(ART)有了很大发展。从早期毒性高、服药负担大的单一疗法,到服药负担更大、效力更强的联合疗法,最后,从2005年至今,我们现在有了服药负担低和每日一次疗法的选择。即使在资源匮乏的环境中,更方便、毒性更小的治疗方案也越来越多。在此期间,人们对ART疗效和毒性方面个体反应差异的认识也在不断发展。主要组织相容性复合体I类等位基因HLA-B*5701与阿巴卡韦超敏反应的强关联,以及它在常规HIV临床实践中的转化应用,作为具有100%阴性预测值的预测标志物,是一个成功案例,也是将药物遗传学应用于临床所面临挑战和取得胜利的一个显著例子。然而,在实际临床实践中,个体生物标志物能明确指导患者治疗将是例外而非惯例。HIV临床实践中非艾滋病合并症的重要性进一步增加了对抗逆转录病毒疗法采取个体化方法的必要性。未来,抗逆转录病毒疗法个体化方法的理想应用可能包括一种综合方法,即结合药物、病毒和宿主(药物遗传学和药物生态学[个体环境中可能随时间动态变化的因素])信息的知识,以指导真正的个性化处方。本综述将聚焦于我们对现有抗逆转录病毒药物疗效和毒性的药物遗传学知识,以及此类信息和方法在当前及未来HIV临床护理中的当前和潜在应用。