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HIV drug resistance tests are here to stay.艾滋病毒耐药性检测将继续存在。
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Phenotypic and genotypic resistance patterns of HIV-1 isolates derived from individuals treated with didanosine and stavudine.从接受去羟肌苷和司他夫定治疗的个体中分离出的HIV-1毒株的表型和基因型耐药模式。
AIDS. 2000 Jan 28;14(2):F9-15. doi: 10.1097/00002030-200001280-00002.
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Genotypic and phenotypic resistance to stavudine after long-term monotherapy. BMS-020 Spanish Study Group.长期单一疗法后对司他夫定的基因型和表型耐药性。BMS - 020西班牙研究小组。
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Diminished HIV-1 sensitivity to stavudine in patients on prolonged therapy occurs only at low levels and cannot be attributed to any single amino acid substitution in reverse transcriptase.长期接受治疗的患者中,HIV-1对司他夫定的敏感性降低仅在低水平出现,且不能归因于逆转录酶中的任何单个氨基酸取代。
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Incidence and predictors of virologic failure of antiretroviral triple-drug therapy in a community-based cohort.基于社区队列的抗逆转录病毒三联疗法病毒学失败的发生率及预测因素
AIDS Res Hum Retroviruses. 1999 Dec 10;15(18):1631-8. doi: 10.1089/088922299309676.
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The pharmacokinetics of lamivudine phosphorylation in peripheral blood mononuclear cells from patients infected with HIV-1.拉米夫定在感染HIV-1患者外周血单核细胞中的磷酸化药代动力学。
AIDS. 1999 Nov 12;13(16):2239-50. doi: 10.1097/00002030-199911120-00006.
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Emergence of zidovudine and multidrug-resistance mutations in the HIV-1 reverse transcriptase gene in therapy-naive patients receiving stavudine plus didanosine combination therapy. STADI Group.
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Drug-resistant genotyping in HIV-1 therapy.HIV-1治疗中的耐药基因分型
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Drug-resistance genotyping in HIV-1 therapy: the VIRADAPT randomised controlled trial.HIV-1治疗中的耐药基因分型:VIRADAPT随机对照试验
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对有多种抗逆转录病毒治疗方案治疗史的HIV感染患者进行的耐药性分析。

Resistance analyses in HIV infected patients with a history of multiple antiretroviral treatment regimens.

作者信息

Plettenberg A, Albrecht D, Lorenzen T, Paech V, Petersen H, Fenner T, Meyer T, Arndt R, Hertogs K, Pauwels R, Weitzel T, Stoehr A

机构信息

General Hospital St Georg, Hamburg, Germany.

出版信息

Sex Transm Infect. 2001 Dec;77(6):449-52. doi: 10.1136/sti.77.6.449.

DOI:10.1136/sti.77.6.449
PMID:11714947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1744404/
Abstract

OBJECTIVE

To assess HIV-1 isolate based resistance profiles from extensively pretreated patients and effects of a resistance guided switch of antiretroviral therapy.

METHODS

In a prospective study phenotypic and genotypic resistance analyses were performed on HIV infected individuals with failure of the current therapy and history of at least three antiretroviral regimens. Antiretroviral therapy was changed according to the results. Viral load and CD4 lymphocyte counts were measured at baseline, after 10 (SD 2), and 24 (2) weeks.

RESULTS

All patients (n=52) failed their actual regimen. Currently versus ever previously taking the specific drug, resistance associated mutations and phenotypic resistance to AZT and 3TC were found in over 80% of individuals; resistance to DDI and D4T was detected in less than 10% of cases. A resistance guided switch of therapy was followed by a median decrease of viral load of 0.5 log10 units after 24 weeks. Individuals resistant to two or more drugs compared with patients with resistance to less than two drugs of ongoing treatment, were switched to a regimen containing DDI, D4T, and a PI or NNRTI. After 10 (SD 2) weeks viral load decrease was pronounced in patients with resistance to at least two drugs in the previous regimen.

CONCLUSIONS

Among different RTI, the profile of clinically relevant resistance indicates pronounced differences when looking at separate drugs. Regarding virological response, in the context of available drugs, resistance tested with currently used methods is of limited value in extensively pretreated patients and seems to have its value primarily in first or second switch of therapy.

摘要

目的

评估接受过大量治疗的患者中基于HIV-1分离株的耐药谱以及耐药性指导下的抗逆转录病毒疗法转换的效果。

方法

在一项前瞻性研究中,对当前治疗失败且至少接受过三种抗逆转录病毒治疗方案的HIV感染者进行了表型和基因型耐药性分析。根据结果更改抗逆转录病毒疗法。在基线、10(标准差2)周和24(2)周后测量病毒载量和CD4淋巴细胞计数。

结果

所有患者(n = 52)当前治疗方案均失败。与曾经服用过特定药物相比,超过80%的个体中发现了与AZT和3TC相关的耐药性突变和表型耐药性;不到10%的病例检测到对DDI和D4T的耐药性。在耐药性指导下进行治疗转换后,24周后病毒载量中位数下降了0.5 log10单位。与正在接受治疗且耐药性少于两种药物的患者相比,对两种或更多种药物耐药的个体被转换为包含DDI、D4T以及一种蛋白酶抑制剂(PI)或非核苷类逆转录酶抑制剂(NNRTI)的治疗方案。在10(标准差2)周后,对前一种治疗方案中至少两种药物耐药的患者病毒载量明显下降。

结论

在不同的核苷类逆转录酶抑制剂(RTI)中,当单独观察每种药物时,临床相关耐药谱显示出明显差异。关于病毒学反应,在现有药物的背景下,用当前使用的方法检测的耐药性在接受过大量治疗的患者中价值有限,其价值似乎主要体现在首次或第二次治疗转换中。