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首页> 外文期刊>Antimicrobial agents and chemotherapy. >Validation of the INNO-LiPA HBV DR assay (version 2) in monitoring hepatitis B virus-infected patients receiving nucleoside analog treatment.
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Validation of the INNO-LiPA HBV DR assay (version 2) in monitoring hepatitis B virus-infected patients receiving nucleoside analog treatment.

机译:在监测接受核苷类似物治疗的乙型肝炎病毒感染患者中,INNO-LiPA HBV DR分析(第2版)的有效性。

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摘要

Hepatitis B virus (HBV) antiviral drug resistance mutations prevent successful outcome of treatment and lead to worsening of liver disease. Detection of its emergence permits opportune treatment with alternative drugs. Unfortunately, the use of newly approved antivirals, including adefovir dipivoxil, emtricitabine, and telbivudine, is also associated with the development of drug resistance, albeit to a lesser extent than the use of lamivudine. The objectives of this work were to assess the performance characteristics (sensitivity and accuracy) of an updated drug resistance test, the INNO-LiPA HBV DR v2, which includes detection of mutations associated with lamivudine, adefovir, emtricitabine, and telbivudine resistance, and to compare the results with consensus sequencing of serum samples from patients treated with HBV antivirals. Diagnostic sensitivity, defined as detection of a positive amplification line on the line probe assay (LiPA) strip, was 94.8% (95% confidence interval [CI], 89.7 to 97.9) after initial testing, increasing to 96.3% (95% CI, 91.6 to 98.8) after repeat test 1 and to 100% (95% CI, 97.3 to 100.0) after repeat test 2. In diagnostic accuracy determinations, full concordance was observed between sequencing and LiPA for 77.0% of the codons tested (620/805 codons [95% CI, 74.0 to 79.9]), whereas LiPA and sequencing were partially concordant 22% of the time (177/805 codons). In 167 out of 177 cases, LiPA detected a wild-type/mutant mixture whereas sequencing detected only one of the two results. Performance testing of the new LiPA test, the INNO-LiPA HBV DR v2, showed convincing diagnostic sensitivity and accuracy. The ability of the test to detect mixed infections and minority viral populations associated with resistance to the current generation of antivirals, including adefovir, emtricitabine, and telbivudine, makes it a useful tool for HBV therapy monitoring.
机译:乙肝病毒(HBV)抗病毒药物耐药性突变会阻止成功的治疗结果,并导致肝脏疾病恶化。检测其出现允许使用替代药物进行适当治疗。不幸的是,使用新批准的抗病毒药,包括阿德福韦酯,恩曲他滨和替比夫定,也与耐药性的发展有关,尽管程度不如拉米夫定。这项工作的目的是评估最新的耐药性测试INNO-LiPA HBV DR v2的性能特征(敏感性和准确性),其中包括检测与拉米夫定,阿德福韦,恩曲他滨和替比夫定耐药相关的突变,以及将结果与接受HBV抗病毒药治疗的患者血清样品的共有序列进行比较。初始测试后,诊断灵敏度定义为在线探针测定(LiPA)试纸条上检测到阳性扩增线,诊断灵敏度为94.8%(95%置信区间[CI],从89.7到97.9),增至96.3%(95%CI,重复测试1后为91.6至98.8),重复测试2后为100%(95%CI,97.3至100.0)。在诊断准确性确定中,对于77.0%的测试密码子(620/805),在测序和LiPA之间观察到完全一致。密码子[95%CI,74.0至79.9]),而LiPA和测序在22%的时间中部分一致(177/805密码子)。在177个案例中的167个案例中,LiPA检测到了野生型/突变体混合物,而测序仅检测到了两个结果之一。新的LiPA测试(INNO-LiPA HBV DR v2)的性能测试显示出令人信服的诊断灵敏度和准确性。该测试能够检测与当前最新一代抗病毒药(包括阿德福韦,恩曲他滨和替比夫定)抗药性相关的混合感染和少数病毒种群,使其成为监测HBV治疗的有用工具。

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