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成功使用 Plasma Preparation Tubes™(PPTs)于 COBAS® AmpliPrep/COBAS® TaqMan® HIV-1 测试。

Successful use of Plasma Preparation Tubes™ (PPTs) in the COBAS® AmpliPrep/COBAS® TaqMan® HIV-1 test.

机构信息

Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA, USA.

出版信息

J Clin Virol. 2013 May;57(1):77-9. doi: 10.1016/j.jcv.2012.12.015. Epub 2013 Jan 16.

Abstract

BACKGROUND

Since switching to the COBAS(®) AmpliPrep/COBAS(®) TaqMan(®) HIV-1 Test, v. 1.0 from the Amplicor HIV-1 Monitor Test, v. 1.5, an increase in detectable viral load results was noted. We were concerned that this was due to the use of Plasma Preparation Tubes (PPT) in this test.

OBJECTIVE

To assess the impact of different pre-analytical processing conditions on HIV-1 viral load results on the COBAS(®) AmpliPrep/COBAS(®) TaqMan(®) HIV-1 Test.

STUDY DESIGN

Sixty-three HIV-infected patients were consented and had 3 PPTs and 1 K2EDTA drawn for HIV-1 viral load testing. Three methods of PPT processing were compared against the referent K2EDTA tube which was spun at 1100 × g for 20 min, poured off and frozen; PPT1 was refrigerated with an additional centrifugation prior to testing, PPT2 was processed similarly to EDTA, and PPT3 was centrifuged, frozen and centrifuged again prior to testing.

RESULTS

PPT1 and PPT3 yielded results that were most similar to the referent EDTA processing, with a concordance correlation coefficient (CCC) of 0.80 and 0.85, compared to PPT2 with CCC of 0.37. Both PPT1 and PPT3 involved additional centrifugation prior to testing. In 26 patients with residual samples from the PPT2 processing, 9 (34.6%) were found to have the presence of proviral DNA, which likely contributed to the elevated HIV-1 RNA viral loads in these individuals.

CONCLUSION

PPTs can be used in the COBAS(®) AmpliPrep/COBAS(®) TaqMan(®) HIV-1 Test with an additional centrifugation in order to avoid misleading elevated HIV-1 RNA viral loads that may change patient management.

摘要

背景

自从切换到 COBAS(®)AmpliPrep/COBAS(®)TaqMan(®)HIV-1 Test,v.1.0 以来,从 Amplicor HIV-1 Monitor Test,v.1.5,检测到的病毒载量结果有所增加。我们担心这是由于该测试中使用了血浆制备管(PPT)。

目的

评估不同的预分析处理条件对 COBAS(®)AmpliPrep/COBAS(®)TaqMan(®)HIV-1 Test 中 HIV-1 病毒载量结果的影响。

研究设计

征得 63 名 HIV 感染患者的同意,并为 HIV-1 病毒载量检测抽取了 3 个 PPT 和 1 个 K2EDTA。将三种 PPT 处理方法与参考 K2EDTA 管进行比较,K2EDTA 管以 1100×g 离心 20 分钟,倒出并冷冻;PPT1 在检测前冷藏并额外离心,PPT2 以类似 EDTA 的方式处理,PPT3 在检测前离心、冷冻并再次离心。

结果

PPT1 和 PPT3 的结果与参考 EDTA 处理最相似,一致性相关系数(CCC)分别为 0.80 和 0.85,而 PPT2 的 CCC 为 0.37。PPT1 和 PPT3 在检测前都需要额外离心。在 26 名患者中,对 PPT2 处理后的残留样本进行检测,发现有 9 名(34.6%)存在前病毒 DNA,这可能导致这些个体的 HIV-1 RNA 病毒载量升高。

结论

可以在 COBAS(®)AmpliPrep/COBAS(®)TaqMan(®)HIV-1 Test 中使用 PPT,在检测前进行额外的离心,以避免导致误导性升高的 HIV-1 RNA 病毒载量,从而改变患者的管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe9c/3684267/5eb85736c03e/nihms471585f1.jpg

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