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首页> 外文期刊>Journal of environmental pathology, toxicology and oncology: official organ of the International Society for Environmental Toxicology and Cancer >Human immunodeficiency virus type 1 pharmacogenomics in clinical practice: relevance of HIV-1 drug resistance testing (Part 1).
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Human immunodeficiency virus type 1 pharmacogenomics in clinical practice: relevance of HIV-1 drug resistance testing (Part 1).

机译:临床实践中的人类1型免疫缺陷病毒药物基因组学:HIV-1耐药性测试的相关性(第1部分)。

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Throughout most of the past century, physicians could offer patients no treatments for infections caused by viruses. The experience with treatment of infection by human immunodeficiency virus (HIV) has changed the way healthcare workers deal with viral infections and has triggered a growing rate of discovery and use of antiviral agents, the first fruits of the expanding genomics revolution. HIV treatment also provides an informative paradigm for pharmacogenomics because control of infection and its consequences is limited by the development of viral drug resistance and by host factors. This report summarizes studies published to date on the significance of testing of HIV-1 resistance to antiretroviral drugs. The only Food and Drug Administration-approved kit for HIV drug resistance testing by genotypic sequencing is commercially available through Visible Genetics, Inc. Genotyping sequencing alone is most likely an adequate test to assist in the therapeutic decision-making process for previous regimen failure, for treatment-naive patients in areas of high prevalence of transmitted resistant virus, and for pregnant women. However, in exceptional cases of highly complex mutation patterns and extensive cross-resistance, it may be useful to obtain a phenotype test, because that result may more easily identify drugs to which virus is least resistant. There are no published clinical trials results on the usefulness of the so-called virtual phenotype over genotypic sequencing alone. Not only has the paradigm of viral pharmacogenomics in the form of HIV genotypic sequencing been useful in treating other viral diseases, but it is also important to the real-life implementation of the growing discipline ofgenomics or molecular medicine. The application of this paradigm to the thousands of potential therapeutic targets that have become available through the various human genome projects will certainly gradually change the landscape of diagnosis and management of many diseases, including cancer.
机译:在整个上个世纪的大部分时间里,医生都无法为患者提供由病毒引起的感染的治疗方法。人类免疫缺陷病毒(HIV)感染治疗的经验改变了医护人员应对病毒感染的方式,并引发了发现和使用抗病毒剂的比率不断上升的趋势,这是基因组学革命不断发展的最初成果。 HIV治疗还为药物基因组学提供了有益的范例,因为感染的控制及其后果受到病毒耐药性发展和宿主因素的限制。本报告总结了迄今为止已发表的有关测试HIV-1对抗逆转录病毒药物的抗性意义的研究。唯一的食品和药物管理局批准的用于基因型测序的HIV耐药性检测的试剂盒可通过Visible Genetics,Inc.商购获得。仅基因分型测序很可能是足够的试剂,可有助于对先前方案失败的治疗决策过程进行评估,例如初治的患者中传播抗性病毒的高发地区以及孕妇。但是,在异常情况非常复杂的突变模式和广泛的交叉耐药性的特殊情况下,进行表型测试可能会很有用,因为该结果可以更轻松地识别出对病毒抵抗力最低的药物。没有所谓的虚拟表型比单独的基因型测序有用的临床试验结果。 HIV基因型测序形式的病毒药物基因组学范例不仅可用于治疗其他病毒性疾病,而且对于不断增长的基因组学或分子医学学科的现实实施也很重要。通过各种人类基因组计划将这种范例应用到成千上万的潜在治疗靶标中,肯定会逐渐改变包括癌症在内的许多疾病的诊断和管理格局。

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