Literature DB >> 19940949

Understanding HIV phenotypic resistance testing: usefulness in managing treatment-experienced patients.

Rodger D MacArthur1.   

Abstract

This review discusses how "virtual" and conventional phenotypic assays establish clinical cutoffs predictive of response in HIV isolates from antiretroviral-experienced patients. Sophisticated phenotypic assays that incorporate linear regression modeling and conventional phenotypic assays have been used to define and validate clinical cutoffs (i.e. the correlation between viral susceptibility and treatment response) for most antiretrovirals, including the newer protease inhibitors. Using these clinical cutoff values, clinical data show that the newer protease inhibitors retain activity against the majority of isolates from treatment-experienced patients and from those with baseline resistance to multiple protease inhibitors. The utility of phenotypic resistance testing methods have therefore been validated in the clinical setting. In summary, HIV drug resistance testing is currently the recommended standard of care for the selection of antiretroviral regimens for HIV-infected patients in multiple clinical settings. An understanding of the basic principles of phenotypic resistance testing is crucial for providing optimal care, particularly for antiretroviral-experienced patients.

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Year:  2009        PMID: 19940949

Source DB:  PubMed          Journal:  AIDS Rev        ISSN: 1139-6121            Impact factor:   2.500


  6 in total

1.  Agreement between an in-house replication competent and a reference replication defective recombinant virus assay for measuring phenotypic resistance to HIV-1 protease, reverse transcriptase, and integrase inhibitors.

Authors:  Francesco Saladini; Alessia Giannini; Adele Boccuto; Ilaria Vicenti; Maurizio Zazzi
Journal:  J Clin Lab Anal       Date:  2017-03-17       Impact factor: 2.352

2.  Novel method for simultaneous quantification of phenotypic resistance to maturation, protease, reverse transcriptase, and integrase HIV inhibitors based on 3'Gag(p2/p7/p1/p6)/PR/RT/INT-recombinant viruses: a useful tool in the multitarget era of antiretroviral therapy.

Authors:  Jan Weber; Ana C Vazquez; Dane Winner; Justine D Rose; Doug Wylie; Ariel M Rhea; Kenneth Henry; Jennifer Pappas; Alison Wright; Nizar Mohamed; Richard Gibson; Benigno Rodriguez; Vicente Soriano; Kevin King; Eric J Arts; Paul D Olivo; Miguel E Quiñones-Mateu
Journal:  Antimicrob Agents Chemother       Date:  2011-05-31       Impact factor: 5.191

3.  Next-Generation Sequencing to Help Monitor Patients Infected with HIV: Ready for Clinical Use?

Authors:  Richard M Gibson; Christine L Schmotzer; Miguel E Quiñones-Mateu
Journal:  Curr Infect Dis Rep       Date:  2014-04       Impact factor: 3.725

4.  Phenotypic and genotypic analyses to guide selection of reverse transcriptase inhibitors in second-line HIV therapy following extended virological failure in Uganda.

Authors:  R L Goodall; D T Dunn; T Pattery; A van Cauwenberge; P Nkurunziza; P Awio; N Ndembi; P Munderi; C Kityo; C F Gilks; P Kaleebu; D Pillay
Journal:  J Antimicrob Chemother       Date:  2014-03-14       Impact factor: 5.790

5.  A simple and cost-saving phenotypic drug susceptibility testing of HIV-1.

Authors:  Yunceng Weng; Ling Zhang; Jianfeng Huang; Jin Zhao; Peifang Luo; Siyuan Bi; Zhengrong Yang; Hai Zhu; Jean-Pierre Allain; Chengyao Li
Journal:  Sci Rep       Date:  2016-09-19       Impact factor: 4.379

6.  Sensitive deep-sequencing-based HIV-1 genotyping assay to simultaneously determine susceptibility to protease, reverse transcriptase, integrase, and maturation inhibitors, as well as HIV-1 coreceptor tropism.

Authors:  Richard M Gibson; Ashley M Meyer; Dane Winner; John Archer; Felix Feyertag; Ezequiel Ruiz-Mateos; Manuel Leal; David L Robertson; Christine L Schmotzer; Miguel E Quiñones-Mateu
Journal:  Antimicrob Agents Chemother       Date:  2014-01-27       Impact factor: 5.191

  6 in total

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