The impact of pharmacogenetics on HIV therapy

被引:18
作者
Mahungu, T. W. [1 ,2 ]
Johnson, M. A. [1 ]
Owen, A. [2 ]
Back, D. J. [2 ]
机构
[1] Royal Free NHS Trust, Dept HIV Med, London NW3 2QG, England
[2] Univ Liverpool, Dept Pharmacol & Therapeut, Liverpool L69 3GF, Merseyside, England
基金
英国医学研究理事会;
关键词
HIV; HAART; pharmacogenetics; pharmacokinetics; pharmacodynamics; REVERSE-TRANSCRIPTASE INHIBITORS; CYP2B6 983T-GREATER-THAN-C POLYMORPHISM; NEVIRAPINE PLASMA-CONCENTRATIONS; TENOFOVIR DISOPROXIL FUMARATE; P-GLYCOPROTEIN EXPRESSION; CYTOCHROME P4502B6 CYP2B6; ANTIRETROVIRAL-THERAPY; VIROLOGICAL RESPONSE; INFECTED PATIENTS; ABACAVIR HYPERSENSITIVITY;
D O I
10.1258/ijsa.2008.008369
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The use of highly active antiretroviral therapy in the treatment of HIV infection has resulted in significant reductions in mortality and morbidity worldwide. However, there is considerable interindividual variability in patient outcomes in terms of drug disposition, drug efficacy and adverse events. The basis of these differences is multifactorial, but host genetics are believed to play a significant part. To date, most attempts to explain this variability have focused on isolated single nucleotide polymorphisms. The most exciting development to date is the discovery of human leukocyte antigen subtype B*5701 (HLA B*5701) as a strong predictor of the abacavir hypersensitivity reaction. There is a gradual move away from single candidate gene analyses towards a high throughput whole genome approach. These studies must be performed on well characterized cohorts and reported associations must be validated in independent, ethnically diverse populations.
引用
收藏
页码:145 / 151
页数:7
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