| Literature DB >> 26494772 |
Eileen Scully1, Ainsley Lockhart2, Lisa Huang3, Yvonne Robles4, Carlos Becerril3, Marisol Romero-Tejeda2, Mary A Albrecht5, Christine D Palmer2, Ronald J Bosch6, Marcus Altfeld7, Daniel R Kuritzkes4, Nina H Lin8.
Abstract
The aging of the human immunodeficiency virus type 1 (HIV-1)-infected population obligates a focus on the interaction between aging, comorbid conditions, and HIV-1. We recruited a cohort of HIV-1-infected men aged ≤ 35 years or ≥ 50 years who were receiving fully suppressive antiretroviral therapy (ART). We analyzed plasma markers of inflammation; T-cell activation, exhaustion, proliferation; and innate cellular subsets and functional capacity. Levels of lipopolysaccharide and the plasma marker of chemokine (C-C motif) ligand 2 were significantly elevated in older HIV-infected men despite comparable cellular phenotypes. Compared with similarly age-stratified uninfected subjects, older HIV-1-infected adults were also more frequently in the upper quartile of soluble CD14 expression.Entities:
Keywords: HIV-1; chemokine; inflammation; monocytes
Mesh:
Substances:
Year: 2015 PMID: 26494772 PMCID: PMC4747622 DOI: 10.1093/infdis/jiv501
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226