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阿巴卡韦超敏反应的药物遗传学:从药物基因组学假设到确证再到临床应用

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

作者信息

Hughes A R, Spreen W R, Mosteller M, Warren L L, Lai E H, Brothers C H, Cox C, Nelsen A J, Hughes S, Thorborn D E, Stancil B, Hetherington S V, Burns D K, Roses A D

机构信息

GlaxoSmithKline Pharmacogenetics, Research Triangle Park, NC 27709, USA.

出版信息

Pharmacogenomics J. 2008 Dec;8(6):365-74. doi: 10.1038/tpj.2008.3. Epub 2008 Mar 11.

Abstract

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-B5701, 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-B5701 screening, avoidance of ABC in HLA-B5701-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-B5701 screening should greatly reduce the incidence of ABC HSR by identifying patients at high risk for ABC HSR before they are treated.

摘要

对阿巴卡韦(ABC)的药物遗传学(PGx)超敏反应(HSR)项目代表了从探索性发现到经过验证的生物标志物的进展。在该项目中,进行了两项回顾性PGx研究,以识别发生ABC HSR风险增加的HIV-1患者,ABC HSR是一种限制治疗且可能危及生命的不良事件。已确定主要组织相容性复合体等位基因HLA-B5701与临床诊断的ABC HSR之间存在强统计学关联,但在不同种族人群中有所不同。随后,引入ABC皮肤贴片试验作为一种研究工具,以补充临床病例确定。在一项评估HLA-B5701筛查临床效用的随机前瞻性研究中,在HLA-B5701阳性患者中避免使用ABC可显著降低临床诊断的ABC HSR,并消除贴片试验阳性的ABC HSR。最后,一项回顾性PGx研究支持了该关联在不同种族中的普遍性。前瞻性HLA-B5701筛查应通过在接受治疗前识别ABC HSR高危患者,大大降低ABC HSR的发生率。

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