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罗氏与 Xpert 检测 HIV-1 RNA 载量的比较:两种技术高度一致,除了罗氏检测到但 Xpert 未检测到的高病毒载量的 CRF02_AG 亚型变异体。

Comparison between Roche and Xpert in HIV-1 RNA quantitation: A high concordance between the two techniques except for a CRF02_AG subtype variant with high viral load titters detected by Roche but undetected by Xpert.

机构信息

Laboratory for Viruses and Molecular Biology, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel; Crusaid Kobler AIDS Center, Tel-Aviv Sourasky Medical Center, Tel-Aviv Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.

Laboratory for Viruses and Molecular Biology, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel; Crusaid Kobler AIDS Center, Tel-Aviv Sourasky Medical Center, Tel-Aviv Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.

出版信息

J Clin Virol. 2017 Aug;93:15-19. doi: 10.1016/j.jcv.2017.05.014. Epub 2017 May 19.

DOI:10.1016/j.jcv.2017.05.014
PMID:28564629
Abstract

BACKGROUND

HIV-1 viral load (VL) testing is important to predict viral progression and to monitor the response to antiretroviral therapy. New HIV-1 VL tests are continuously introduced to the market. Their performance is usually compared to Abbott and/or Roche HIV-1 VL assays, as reference. The Xpert HIV-1 VL test was recently introduced, but its performance compared to Roche has not been sufficiently studied.

OBJECTIVES

To compare the Xpert assay with Roche and to assess its use in the HIV clinical laboratory.

STUDY DESIGN

A total of 383 plasma samples of HIV-1 infected patients previously tested by Roche, were retrospectively tested by Xpert to determine concordance between the two assays. Samples included a diversity of HIV-1 subtypes and a wide range of VLs.

RESULTS

There was a high concordance between the two assays, except for a CRF02_AG subtype variant with high VL titters, that was detected by Roche but undetected by Xpert. The 5' long terminal repeat gene region of this virus, targeted by the Xpert assay, was amplified and sequenced. A 25 nucleotide insert was identified, but was unmatched to any known sequences of HIV-1. This particular insert, however could not explain the false-negativity by the Xpert assay.

CONCLUSIONS

This study underlines the challenge to routine VL testing due to the high genetic diversity of HIV-1. Clinicians should, therefore be advised that a negative VL in cases where the clinical picture does not match the laboratory report, might in fact be, a false-negative result of the VL assay.

摘要

背景

HIV-1 病毒载量 (VL) 检测对于预测病毒进展和监测抗逆转录病毒治疗的反应非常重要。新的 HIV-1 VL 检测方法不断推向市场。它们的性能通常与 Abbott 和/或 Roche HIV-1 VL 检测方法进行比较,作为参考。Xpert HIV-1 VL 检测最近推出,但尚未充分研究其与罗氏的性能比较。

目的

比较 Xpert 检测与罗氏的检测,并评估其在 HIV 临床实验室中的应用。

研究设计

共回顾性检测了 383 份先前用罗氏检测的 HIV-1 感染患者的血浆样本,以确定两种检测方法之间的一致性。样本包括多种 HIV-1 亚型和广泛的 VL 范围。

结果

两种检测方法之间存在高度一致性,除了一种高 VL 滴度的 CRF02_AG 亚型变异体,罗氏检测到但 Xpert 未检测到。该病毒的 5'长末端重复基因区域是 Xpert 检测的靶标,该区域被扩增和测序。鉴定出一个 25 个核苷酸的插入片段,但与 HIV-1 的任何已知序列都不匹配。然而,这个特定的插入片段并不能解释 Xpert 检测的假阴性。

结论

本研究强调了由于 HIV-1 的高度遗传多样性,常规 VL 检测面临的挑战。因此,临床医生应该注意到,如果临床情况与实验室报告不匹配,VL 呈阴性,实际上可能是 VL 检测的假阴性结果。

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