Toll-like receptor ligands induce human T cell activation and death, a model for HIV pathogenesis

Abstract

Background: Recently, heightened systemic translocation of microbial products was found in persons with chronic HIV infection and this was linked to immune activation and CD4+ T cell homeostasis. Methodology: We examined here the effects of microbial Toll-like receptor (TLR) ligands on T cell activation in vitro. Conclusion/Findings: We show that exposure to TLR ligands results in activation of memory and effector CD4+ and CD8+ T cells. After exposure to each of 8 different ligands that activate TLRs 2, 3, 4, 5, 7, 8, and 9, CD8+ T cells are activated and gain expression of the C type lectin CD69 that may promote their retention in lymphoid tissues. In contrast, CD4+ T cells rarely increase CD69 expression but instead enter cell cycle. Despite activation and cell cycle entry, CD4+ T cells divide poorly and instead, disproportionately undergo activation-induced cell death. Systemic exposure to TLR agonists may therfore increase immune activation, effector cell sequestration in lymphoid tissues and T cell turnover. These events may contribute to the pathogenesis of immune dysfunction and CD4+ T cell losses in chronic infection-with the human immunodeficiency virus. © 2008 Funderburg et al.