| Literature DB >> 27354367 |
Theodoros Kelesidis1, Carlee Moser2, James H Stein3, Todd T Brown4, Thuy Tien T Tran2, Heather J Ribaudo2, Michael P Dube5, Otto O Yang1, Judith S Currier1, Grace A McComsey6.
Abstract
It is unclear whether differential roles of CD4(+) versus CD8(+) T-cell senescence/exhaustion and effects of antiretroviral therapy (ART) on these processes may contribute to morbidity in treated human immunodeficiency virus type 1 (HIV) infection. In a prospective 96-week trial, 328 HIV-infected ART-naive participants were randomly assigned to receive tenofovir-emtricitabine plus either atazanavir/ritonavir, darunavir/ritonavir, or raltegravir. Markers of CD4(+) T-cell senescence (ie, the percentage of CD28(-)CD57(+) cells among CD4(+) T cells ) and CD4(+)/CD8(+) T-cell exhaustion (ie, the percentage of PD-1(+) cells among CD4(+)/CD8(+) T cells) decreased after ART. There were no changes in markers of CD8(+) T-cell senescence after ART and no differential changes in all markers in ART groups. Senescent CD4(+) and CD8(+) T cells may have differential roles in HIV pathogenesis.Entities:
Keywords: antiretroviral therapy; biomarkers; human immunodeficiency virus; immune activation; inflammation
Mesh:
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Year: 2016 PMID: 27354367 PMCID: PMC4978379 DOI: 10.1093/infdis/jiw253
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226