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应用 Geenius 快速确证检测试剂与 INNO-LIA、New Lav 和 Blot 2.2 检测试剂对比,对近期 HIV-1 感染进行分期。

Staging of recent HIV-1 infection using Geenius rapid confirmatory assay compared to INNO-LIA, New Lav and Blot 2.2 assays.

机构信息

Pathogenesis and Control of Chronic Infections, INSERM, EFS, Université de Montpellier, Montpellier, France; CHU Montpellier, Department of Bacteriology-Virology and Department of Infectious Diseases, Montpellier, France.

Pathogenesis and Control of Chronic Infections, INSERM, EFS, Université de Montpellier, Montpellier, France.

出版信息

J Clin Virol. 2017 Oct;95:47-51. doi: 10.1016/j.jcv.2017.08.003. Epub 2017 Aug 18.

Abstract

BACKGROUND

Besides confirmation of HIV seropositivity, Western Blot (WB) assays play an important role for identification of recent infection based on incomplete antibody reactivity and lack of p31 band.

OBJECTIVES

We evaluated the capacities of the Geenius™ HIV1/2 Confirmatory Assay (Bio-Rad), a new generation rapid confirmatory assay based on immune-chromatography and automated reading, for staging of HIV-1 infection.

STUDY DESIGN

Sixteen samples collected during early HIV-1 infections (Fiebig stage III-VI) were tested using the Geenius assay, and compared to HIV Blot 2.2 WB assay (MP Diagnostics), New Lav Blot I WB assay (Bio-Rad) and INNO-LIA™ HIV I/II Score Dot Blot assay (Fujirebio). Results obtained with Geenius and INNO LIA in 47 newly diagnosed chronic HIV-1 infections were also compared.

RESULTS

The p24 band was less frequently detected in early HIV-1 infections using the Geenius (3/16) compared to the New Lav (15/16, p<0.0001), INNO-LIA (13/16, p=0.0011), and Blot 2.2 (13/16, p=0.0011). Testing samples collected during chronic infection allowed to confirm that p31 band and complete Gag, Pol, Env profiles were less frequently observed using the Geenius assay compared to the INNO LIA assay (p=0.027 for p31, and p=0.0015 for complete profile).

CONCLUSIONS

The Geenius assay is a simple and rapid test showing a high sensitivity to detect Env bands and to confirm HIV-1 seropositivity during the early phases of infection. However, this test is less suitable for distinguishing between later stages of acute and chronic infections because of a reduced sensitivity to detect the p31 and p24 bands compared to INNO LIA and New Lav assays.

摘要

背景

除了确认 HIV 血清阳性外,Western Blot(WB)检测在基于不完全抗体反应和缺乏 p31 带的情况下对识别近期感染也具有重要作用。

目的

我们评估了新一代基于免疫层析和自动读取的快速确证检测试剂 Geenius™ HIV1/2 确证检测(Bio-Rad)在 HIV-1 感染分期中的能力。

研究设计

使用 Geenius 检测试剂盒检测了 16 例早期 HIV-1 感染(Fiebig 分期 III-VI)期间采集的样本,并与 HIV Blot 2.2 WB 检测试剂盒(MP Diagnostics)、New Lav Blot I WB 检测试剂盒(Bio-Rad)和 INNO-LIA™ HIV I/II Score Dot Blot 检测试剂盒(Fujirebio)进行比较。还比较了 Geenius 和 INNO LIA 在 47 例新诊断的慢性 HIV-1 感染中的检测结果。

结果

与 New Lav(15/16,p<0.0001)、INNO-LIA(13/16,p=0.0011)和 Blot 2.2(13/16,p=0.0011)相比,Geenius 检测试剂盒在早期 HIV-1 感染中检测到 p24 带的频率较低(3/16)。检测慢性感染采集的样本证实,与 INNO LIA 检测试剂盒相比,Geenius 检测试剂盒检测到 p31 带和完整 Gag、Pol、Env 谱的频率较低(p=0.027 用于 p31,p=0.0015 用于完整谱)。

结论

Geenius 检测试剂盒是一种简单快速的检测方法,在感染早期检测 Env 带和确认 HIV-1 血清阳性具有较高的敏感性。然而,与 INNO LIA 和 New Lav 检测试剂盒相比,该检测试剂盒对 p31 和 p24 带的检测敏感性降低,因此不太适合区分急性和慢性感染的后期阶段。

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