| Literature DB >> 20844049 |
Shannon M Murray1, Carrie M Down, David R Boulware, William M Stauffer, Winston P Cavert, Timothy W Schacker, Jason M Brenchley, Daniel C Douek.
Abstract
Increased levels of activated T cells are a hallmark of the chronic stage of human immunodeficiency virus (HIV) infection and are highly correlated with HIV disease progression. We evaluated chloroquine (CQ) as a potential therapy to reduce immune activation during HIV infection. We found that the frequency of CD38(+) HLA-DR(+) CD8 T cells, as well as Ki-67 expression in CD8 and CD4 T cells, was significantly reduced during CQ treatment. Our data indicate that treatment with CQ reduces systemic T-cell immune activation and, thus, that its use may be beneficial for certain groups of HIV-infected individuals.Entities:
Mesh:
Substances:
Year: 2010 PMID: 20844049 PMCID: PMC2977889 DOI: 10.1128/JVI.01466-10
Source DB: PubMed Journal: J Virol ISSN: 0022-538X Impact factor: 5.103