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2
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J Virol Methods. 2007 Dec;146(1-2):14-21. doi: 10.1016/j.jviromet.2007.05.024. Epub 2007 Jul 12.
3
The measurement of HIV-1 viral load in resource-limited settings: how and where?资源有限环境下的HIV-1病毒载量检测:方法与地点?
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J Clin Virol. 2007 May;39(1):9-15. doi: 10.1016/j.jcv.2006.12.026. Epub 2007 Mar 23.
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A novel internally controlled real-time reverse transcription-PCR assay for HIV-1 RNA targeting the pol integrase genomic region.一种针对HIV-1 RNA的新型内控实时逆转录PCR检测方法,该方法靶向pol整合酶基因组区域。
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7
HIV-1 viral load assays for resource-limited settings.针对资源有限环境的HIV-1病毒载量检测
PLoS Med. 2006 Oct;3(10):e417. doi: 10.1371/journal.pmed.0030417.
8
Reverse transcriptase activity for quantitation of HIV-1 subtype C in plasma: relation to RNA copy number and CD4 T-cell count.用于定量血浆中HIV-1 C亚型的逆转录酶活性:与RNA拷贝数和CD4 T细胞计数的关系。
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9
Comparison of two human immunodeficiency virus (HIV) RNA surrogate assays to the standard HIV RNA assay.两种人类免疫缺陷病毒(HIV)RNA替代检测方法与标准HIV RNA检测方法的比较。
J Clin Microbiol. 2005 Dec;43(12):5950-6. doi: 10.1128/JCM.43.12.5950-5956.2005.
10
Human immunodeficiency virus (HIV) reverse transcriptase activity correlates with HIV RNA load: implications for resource-limited settings.人类免疫缺陷病毒(HIV)逆转录酶活性与HIV RNA载量相关:对资源有限环境的影响。
J Clin Microbiol. 2005 Aug;43(8):3793-6. doi: 10.1128/JCM.43.8.3793-3796.2005.

用于监测儿童和成人患者HIV病毒载量的低成本Cavidi ExaVir Load检测法的评估。

Assessment of the low-cost Cavidi ExaVir Load assay for monitoring HIV viral load in pediatric and adult patients.

作者信息

Greengrass Vicki, Lohman Barbera, Morris Lisa, Plate Megan, Steele Pauline M, Walson Judd L, Crowe Suzanne M

机构信息

Clinical Research Laboratory, Centre for Virology, Burnet Institute, Melbourne, Australia.

出版信息

J Acquir Immune Defic Syndr. 2009 Nov 1;52(3):387-90. doi: 10.1097/QAI.0b013e3181b05f62.

DOI:10.1097/QAI.0b013e3181b05f62
PMID:19617845
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2784031/
Abstract

BACKGROUND

Viral load (VL) is a critical marker for monitoring HIV disease progression and response to antiretroviral therapy. In resource-constrained settings, there is a need for a simple and inexpensive assay to monitor infected adults and children.

METHODS

We compared versions 2 and 3 of the ExaVir Load assay, Cavidi AB (HIV RT) with the Roche, COBAS Amplicor HIV-1 Monitor assay (HIV RNA) for quantifying HIV VL.

RESULTS

The HIV RT version 2 assay showed good sensitivity with detection in 94% of samples with HIV RNA >1000 copies per milliliter. Adult samples were tested using HIV RT version 2 (n = 35) and version 3 (n = 23) assays with plasma volumes of 1 mL (recommended), 0.5 mL and 0.25 mL in comparison with HIV RNA. The HIV RT and HIV RNA assay results were comparable when tested using different volumes. Comparison of results from pediatric samples (n = 27), tested using 1 mL and a smaller volume by HIV RT version 2 were not significantly different.

CONCLUSIONS

The HIV RT assay was comparable to the HIV RNA assay with sensitivity approaching that of HIV RNA. Smaller volumes than the recommended 1 mL can be used, improving utility of this assay for pediatric monitoring.

摘要

背景

病毒载量(VL)是监测HIV疾病进展及对抗逆转录病毒治疗反应的关键指标。在资源有限的环境中,需要一种简单且廉价的检测方法来监测受感染的成人和儿童。

方法

我们将Cavidi AB公司的ExaVir Load检测法(HIV RT)第2版和第3版与罗氏公司的COBAS Amplicor HIV-1 Monitor检测法(HIV RNA)进行比较,以定量检测HIV病毒载量。

结果

HIV RT第2版检测法显示出良好的灵敏度,在HIV RNA每毫升>1000拷贝的样本中,94%能检测到。使用HIV RT第2版(n = 35)和第3版(n = 23)检测法对成人样本进行检测,血浆体积分别为1 mL(推荐量)、0.5 mL和0.25 mL,并与HIV RNA检测结果进行比较。当使用不同体积的样本进行检测时,HIV RT检测法和HIV RNA检测法的结果具有可比性。对儿科样本(n = 27)使用1 mL及更小体积样本通过HIV RT第2版检测法进行检测,结果无显著差异。

结论

HIV RT检测法与HIV RNA检测法相当,其灵敏度接近HIV RNA检测法。可以使用比推荐的1 mL更小的体积,提高该检测法在儿科监测中的实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b44c/2784031/b09dd3a32042/nihms139795f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b44c/2784031/26b1e8264a08/nihms139795f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b44c/2784031/b09dd3a32042/nihms139795f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b44c/2784031/26b1e8264a08/nihms139795f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b44c/2784031/b09dd3a32042/nihms139795f2.jpg