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Pharmacogenetics of antiretrovirals.

机译:抗逆转录病毒药的药物遗传学。

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The introduction of highly active antiretroviral therapy (HAART) as standard of care has changed the natural history of HIV infection into a manageable chronic disease requiring long-term antiretroviral (ARV) treatment. However, response to HAART is often limited by the occurrence of toxicity or by the emergence of drug resistance. Antiretroviral treatment is characterized by differing rates of adverse events and responses. Genetic variations between human beings account for a relevant proportion of this variability. A relevant number of associations between human genetic variants and predisposition to adverse events have been described and for some antiretroviral drugs a clear and casual genotype-phenotype correlation has already been established. The strong association between abacavir hypersensitivity reaction and HLA-B*5701 has been demonstrated in both observational and blinded randomized clinical trials in racially diverse populations and represents the best example of the clinical utility of pharmacogenetic screening in HIV medicine. Genotyping for HLA-B*5701 before prescribing an abacavir containing regimen has been introduced into routine clinical practice as the standard of care for all patients. Other well-established associations include CYP2B6 alleles and efavirenz central nervous system side effects, UGT1A1 alleles and atazanavir-associated hyperbilirubinemia and HLA class II allele HLA-DRB*0101 and nevirapine-associated hypersensitivity. Despite genetic associations having been described for peripheral neuropathy, lipodystrophy, hyperlipidaemia, pancreatitis and renal proximal tubulopathy, numerous barriers exist to the successful introduction of widespread genetic testing to the clinic. Future prospects point in the direction of individualization of antiretroviral therapy through insights from host genetics. The present paper is aimed to provide a comprehensive review of the published literature and to summarize the state of research in this area. This article forms part of a special issue of Antiviral Research marking the 25th anniversary of antiretroviral drug discovery and development, Vol 85, issue 1, 2010.
机译:引入高活性抗逆转录病毒疗法(HAART)作为护理标准,已将HIV感染的自然史改变为需要长期抗逆转录病毒(ARV)治疗的可控制的慢性疾病。但是,对HAART的反应通常受到毒性作用或耐药性的限制。抗逆转录病毒疗法的特点是不良事件和反应的发生率不同。人与人之间的遗传变异是造成这种变异的重要原因。已经描述了人类遗传变异与不良事件易感性之间的相关数目的关联,并且对于某些抗逆转录病毒药物,已经建立了清晰而随意的基因型与表型的相关性。阿巴卡韦超敏反应与HLA-B * 5701之间的密切联系已在不同种族的人群的观察性和盲性随机临床试验中得到证实,并且代表了药物遗传学筛查在HIV药物中临床应用的最佳实例。在处方含阿巴卡韦的方案之前,对HLA-B * 5701进行基因分型已作为常规治疗方法引入所有患者。其他公认的关联包括CYP2B6等位基因和依非韦伦中枢神经系统副作用,UGT1A1等位基因和阿扎那韦相关的高胆红素血症和HLA II类等位基因HLA-DRB * 0101和奈韦拉平相关的超敏反应。尽管已经描述了与周围神经病,脂肪营养不良,高脂血症,胰腺炎和肾近端肾小管病变的遗传相关性,但成功地将广泛的遗传学检测引入临床仍然存在许多障碍。通过宿主遗传学的见识,未来的前景指向了抗逆转录病毒疗法的个体化方向。本文旨在提供对已发表文献的全面综述,并总结该领域的研究现状。本文是《抗病毒研究》特刊(纪念抗逆转录病毒药物发现和开发25周年)的一部分,第85卷,第1期,2010年。

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