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在挽救治疗下仍处于病毒学失败的接受过恩夫韦肽治疗的患者中恩夫韦肽耐药突变的动态变化

Dynamics of enfuvirtide resistance mutations in enfuvirtide-experienced patients remaining in virological failure under salvage therapy.

作者信息

Charpentier Charlotte, Jenabian Mohammad Ali, Piketty Christophe, Karmochkine Marina, Tisserand Pascaline, Laureillard Didier, Bélec Laurent, Si-Mohamed Ali, Weiss Laurence

机构信息

Laboratoire de Virologie, Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Paris, France.

出版信息

Scand J Infect Dis. 2011 May;43(5):373-9. doi: 10.3109/00365548.2011.552520. Epub 2011 Feb 22.

Abstract

BACKGROUND

Evaluation of the dynamics of enfuvirtide (ENF) resistance mutations after ENF withdrawal in patients with virological failure under salvage therapy may be helpful to optimize the management of ENF in human immunodeficiency virus (HIV)-infected patients.

METHODS

Seven patients with a failing ENF-containing regimen, initiated for at least 3 months (median 6.4 months, range 3-14), were included and followed up prospectively at the time of virological failure. Genotypic analysis of the gp41 region by bulk sequencing and clonal analysis was performed in plasma and/or peripheral blood mononuclear cells to detect ENF resistance mutations.

RESULTS

Genotypic profiles of ENF-resistant variants at ENF discontinuation were as follows: V38A in 3 patients, V38A+N42T+N43D in 1 patient, N43D in 2 patients, and N43K in 1 patient. Clonal analysis showed that maintaining ENF treatment after virological failure has an impact on both (1) the number of resistance profiles detected, and (2) the time of persistence of ENF-resistant variants. ENF-resistant variants were archived in HIV DNA in 5/7 patients. At 1 month after ENF withdrawal, no significant increase in HIV-1 viral load was observed.

CONCLUSION

The persistence of ENF-resistant variants was found to be correlated to exposure time to failing drug. ENF withdrawal should be considered in patients with virological failure to preserve the possible efficacy of ENF recycling or upcoming entry inhibitors.

摘要

背景

对于接受挽救治疗且病毒学治疗失败的患者,评估停用恩夫韦肽(ENF)后其耐药突变的动态变化,可能有助于优化人类免疫缺陷病毒(HIV)感染患者的恩夫韦肽管理。

方法

纳入7例接受含恩夫韦肽方案治疗失败的患者,该方案至少已启动3个月(中位数6.4个月,范围3 - 14个月),并在病毒学治疗失败时进行前瞻性随访。对血浆和/或外周血单个核细胞进行gp41区域的基因分型分析,采用批量测序和克隆分析检测恩夫韦肽耐药突变。

结果

停用恩夫韦肽时,恩夫韦肽耐药变异体的基因分型情况如下:3例患者为V38A,1例患者为V38A + N42T + N43D,2例患者为N43D,1例患者为N43K。克隆分析表明,病毒学治疗失败后继续使用恩夫韦肽治疗对以下两方面均有影响:(1)检测到的耐药谱数量;(2)恩夫韦肽耐药变异体的持续存在时间。7例患者中有5例的恩夫韦肽耐药变异体存在于HIV DNA中。停用恩夫韦肽1个月后,未观察到HIV - 1病毒载量显著增加。

结论

发现恩夫韦肽耐药变异体的持续存在与暴露于无效药物的时间相关。对于病毒学治疗失败的患者,应考虑停用恩夫韦肽,以保留恩夫韦肽再利用或即将使用的进入抑制剂可能的疗效。

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