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首页> 外文期刊>JAIDS: Journal of acquired immune deficiency syndromes >Performance Evaluation of the New HIV-1 Quantification Assay, Xpert HIV-1 Viral Load, on a Wide Panel of HIV-1 Variants
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Performance Evaluation of the New HIV-1 Quantification Assay, Xpert HIV-1 Viral Load, on a Wide Panel of HIV-1 Variants

机译:新的HIV-1定量检测方法Xpert HIV-1病毒载量在各种HIV-1变异体上的性能评估

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Objective:To evaluate the quantification performance of the new Cepheid GeneXpert HIV-1 viral load assay, on a wide panel of HIV-1 variants.Methods:Clinical performance was evaluated relative to the Abbott RealTime HIV-1 assay on 285 HIV-1 seropositive samples selected to cover the assays quantification range (40 copies/mL-10,000,000 copies/mL), and included RNA undetectable or detected seropositive samples. The panel comprised 120 subtype B, 150 non-B, and 15 nontypable clinical samples; serial dilutions of 18 viral supernatants representative of the divergent viruses of HIV-1 groups N, O, and P were also tested.Results:Based on samples selected according to the Abbott assay viral loads (VL), the Cepheid assay detected or quantified 222/285 (78%) samples and the Abbott assay 240/285 (84%). Xpert yielded VLs for 162 (76%) of the 213 quantifiable samples with Abbott. This difference corresponded to 51 samples with VL >40 copies/mL by the Abbott assay (all below 200 copies/mL) but detected (n = 40) or undetectable (n = 11) by the Cepheid assay. VL of samples quantifiable by both assays (n = 162) showed very strong correlation, with a Spearman correlation coefficient of 0.985 and a Bland-Altman's mean of differences of -0.01. Performance for quantification of the non-M samples showed very good correlation, with significantly higher values with Cepheid for the group N and 2 group O samples.Conclusions:Our study showed that the Xpert HIV-1 VL assay offered very good performance for detection and quantification of the current HIV-1 genetic diversity; differences reported at the threshold could be an issue and requires further evaluations. The practicability of this new assay makes it suitable for low-income countries, where it could facilitate and improve follow-up of patients, as well as for high-income regions.
机译:目的:在各种HIV-1变异体上评估新造父变母GeneXpert HIV-1病毒载量测定的定量性能。方法:相对于Abbott RealTime HIV-1测定法对285种HIV-1血清阳性的临床表现进行评估选择的样本要覆盖测定的定量范围(40份/ mL-10,000,000份/ mL),并包括不可检测或检测到的血清阳性样品。该小组包括120个B型亚型,150个非B型和15个非典型临床样本;还检测了18种代表HIV-1 N,O和P异种病毒的病毒上清液的系列稀释液。结果:根据Abbott分析病毒载量(VL)选择的样本,检测或定量了Cepheid分析222 / 285(78%)样品和Abbott分析240/285(84%)。 Xpert用雅培生产的213个可量化样品中的162个(76%)产生了VLs。该差异对应于通过Abbott分析得出的VL> 40拷贝/ mL的51个样品(均低于200拷贝/ mL),但通过造父变星分析检测到(n = 40)或无法检测到(n = 11)。两种测定均可量化的样品的VL(n = 162)显示出非常强的相关性,Spearman相关系数为0.985,Bland-Altman的均值差为-0.01。非M样品的定量性能表现出很好的相关性,N组和O组2个样品的造父变色值明显更高。结论:我们的研究表明Xpert HIV-1 VL检测对于检测和检测Xpert HIV表现出非常好的性能。量化目前的HIV-1遗传多样性;在阈值处报告的差异可能是一个问题,需要进一步评估。这种新方法的实用性使其适用于可以促进和改善患者随访的低收入国家以及高收入地区。

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