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Prevalence of CXCR4 Tropism among Antiretroviral‐Treated HIV‐1–Infected Patients with Detectable Viremia
Author(s) -
Peter W. Hunt,
P. Richard Harrigan,
Wei Huang,
Michael Bates,
David Williamson,
Joseph M. McCune,
Richard W. Price,
Serena Spudich,
Harry Lampiris,
Rebecca Hoh,
Teri Leigler,
Jeffrey N. Martin,
Steven G. Deeks
Publication year - 2006
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/507312
Subject(s) - viremia , virology , lentivirus , cxcr4 , biology , tropism , immunology , tissue tropism , viral load , virus , human immunodeficiency virus (hiv) , viral disease , medicine , chemokine , immune system
Although CXCR4-tropic viruses are relatively uncommon among untreated human immunodeficiency virus (HIV)-infected individuals except during advanced immunodeficiency, the prevalence of CXCR4-tropic viruses among treated patients with detectable viremia is unknown. To address this issue, viral coreceptor usage was measured with a single-cycle recombinant-virus phenotypic entry assay in treatment-naive and treated HIV-infected participants with detectable viremia sampled from 2 clinic-based cohorts. Of 182 treated participants, 75 (41%) harbored dual/mixed or X4-tropic viruses, compared with 178 (18%) of the 976 treatment-naive participants (P<.001). This difference remained significant after adjustment for CD4+ T cell count and CCR5 Delta 32 genotype. Enrichment for dual/mixed/X4-tropic viruses among treated participants was largely but incompletely explained by lower pretreatment nadir CD4 + T cell counts. CCR5 inhibitors may thus be best strategically used before salvage therapy and before significant CD4 + T cell depletion.

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