Literature DB >> 23332979

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

Colleen S Kraft1, José Nilo G Binongo, Eileen M Burd, Molly E Eaton, Cindy B McCloskey, Helen Fernandes, Charles E Hill, Angela M Caliendo.   

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.
Copyright © 2012 Elsevier B.V. All rights reserved.

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Year:  2013        PMID: 23332979      PMCID: PMC3684267          DOI: 10.1016/j.jcv.2012.12.015

Source DB:  PubMed          Journal:  J Clin Virol        ISSN: 1386-6532            Impact factor:   3.168


  13 in total

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5.  Coamplification of HIV-1 proviral DNA and viral RNA in assays used for quantification of HIV-1 RNA.

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8.  Increased detectability of plasma HIV-1 RNA after introduction of a new assay and altered specimen-processing procedures.

Authors:  Peter F Rebeiro; Asghar Kheshti; Sally S Bebawy; Samuel E Stinnette; Husamettin Erdem; Yi-Wei Tang; Timothy R Sterling; Stephen P Raffanti; Richard T D'Aquila
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9.  Megakaryocytes of human immunodeficiency virus-infected individuals express viral RNA.

Authors:  D Zucker-Franklin; Y Z Cao
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10.  Distribution of HIV type 1 (HIV-1) in blood components: detection and significance of high levels of HIV-1 associated with platelets.

Authors:  T H Lee; R R Stromberg; J W Heitman; L Sawyer; C V Hanson; M P Busch
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1.  Estimation of measurement error in plasma HIV-1 RNA assays near their limit of quantification.

Authors:  Viviane D Lima; Lu Wang; Chanson Brumme; Lang Wu; Julio S G Montaner; P Richard Harrigan
Journal:  PLoS One       Date:  2017-02-02       Impact factor: 3.240

2.  Reliability of plasma HIV viral load testing beyond 24 hours: Insights gained from a study in a routine diagnostic laboratory.

Authors:  Diana Hardie; Stephen Korsman; Sharifa Ameer; Lara Vojnov; Nei-Yuan Hsiao
Journal:  PLoS One       Date:  2019-07-03       Impact factor: 3.240

3.  Systematic review of the accuracy of plasma preparation tubes for HIV viral load testing.

Authors:  Robert Luo; Jessica Markby; Jilian Sacks; Lara Vojnov
Journal:  PLoS One       Date:  2019-11-21       Impact factor: 3.240

  3 in total

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