Reliable genotypic tropism tests for the major HIV-1 subtypes.
Abstract
Over the past decade antiretroviral drugs have dramatically improved the prognosis
for HIV-1 infected individuals, yet achieving better access to vulnerable populations
remains a challenge. The principal obstacle to the CCR5-antagonist, maraviroc, from
being more widely used in anti-HIV-1 therapy regimens is that the pre-treatment genotypic
"tropism tests" to determine virus susceptibility to maraviroc have been developed
primarily for HIV-1 subtype B strains, which account for only 10% of infections worldwide.
We therefore developed PhenoSeq, a suite of HIV-1 genotypic tropism assays that are
highly sensitive and specific for establishing the tropism of HIV-1 subtypes A, B,
C, D and circulating recombinant forms of subtypes AE and AG, which together account
for 95% of HIV-1 infections worldwide. The PhenoSeq platform will inform the appropriate
use of maraviroc and future CCR5 blocking drugs in regions of the world where non-B
HIV-1 predominates, which are burdened the most by the HIV-1 pandemic.
Type
Journal articleSubject
HumansHIV-1
HIV Infections
Cyclohexanes
Triazoles
Peptide Fragments
Receptors, CCR5
HIV Envelope Protein gp120
Computational Biology
Amino Acid Sequence
Genotype
Phenotype
Mutation
Algorithms
Viral Tropism
CCR5 Receptor Antagonists
Maraviroc
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https://hdl.handle.net/10161/24539Published Version (Please cite this version)
10.1038/srep08543Publication Info
Cashin, Kieran; Gray, Lachlan R; Harvey, Katherine L; Perez-Bercoff, Danielle; Lee,
Guinevere Q; Sterjovski, Jasminka; ... Gorry, Paul R (2015). Reliable genotypic tropism tests for the major HIV-1 subtypes. Scientific reports, 5(1). pp. 8543. 10.1038/srep08543. Retrieved from https://hdl.handle.net/10161/24539.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
James Francis Demarest
Adjunct Assistant Professor in the Department of Immunology
I have >30 years of experience in the pre-clinical, clinical, and translational
research space. Twenty-three of those years are in the pharma R&D context where I
also gained experience in diagnostics, product commercialization and life-cycle management,
interactions with Regulatory Authorities, Key Opinion Leaders (globally), and establishment/maintenance
of public-private partnerships. My career trajectory took me from NIH (Dr. Anthony
Fauci’s laboratory), to Duke Un

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