Pharmacogenetics of hypersensitivity to abacavir: from PGx hypothesis to confirmation to clinical utility

被引:55
作者
Hughes, A. R. [1 ]
Spreen, W. R. [2 ]
Mosteller, M. [1 ]
Warren, L. L. [1 ]
Lai, E. H. [1 ]
Brothers, C. H. [2 ]
Cox, C. [3 ]
Nelsen, A. J. [1 ]
Hughes, S. [4 ]
Thorborn, D. E. [5 ]
Stancil, B. [2 ]
Hetherington, S. V. [2 ]
Burns, D. K. [1 ]
Roses, A. D. [1 ]
机构
[1] GlaxoSmithKline Pharmacogenet, Res Triangle Pk, NC 27709 USA
[2] Infect Dis Med Dev Ctr, Res Triangle Pk, NC USA
[3] GlaxoSmithKline Pharmacogenet, Harlow, Essex, England
[4] Infect Dis Med Dev Ctr, Greenford, Middx, England
[5] Pharmaceut Europe, Brentford, England
关键词
abacavir; hypersensitivity; pharmacogenetics; drug safety; HLA-B*5701;
D O I
10.1038/tpj.2008.3
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
The hypersensitivity (HSR) to abacavir (ABC) pharmacogenetics (PGx) program represents the progression from an exploratory discovery to a validated biomarker. Within the program, two retrospective PGx studies were conducted to identify HIV-1 patients at increased risk for ABC HSR, a treatment-limiting and potentially life-threatening adverse event. A strong statistical association between the major histocompatibility complex allele, HLA-B*5701, and clinically diagnosed ABC HSR was identified but varied between racial populations. Subsequently, ABC skin patch testing was introduced as a research tool to supplement clinical case ascertainment. In a randomized, prospective study evaluating the clinical utility of HLA-B*5701 screening, avoidance of ABC in HLA-B*5701-positive patients significantly reduced clinically diagnosed ABC HSR and eliminated patch test-positive ABC HSR. Finally, a retrospective PGx study supports the generalizability of the association across races. Prospective HLA-B*5701 screening should greatly reduce the incidence of ABC HSR by identifying patients at high risk for ABC HSR before they are treated.
引用
收藏
页码:365 / 374
页数:10
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