Ligand-Independent Exhaustion of Killer Immunoglobulin-Like Receptor-Positive CD8 + T Cells in Human Immunodeficiency Virus Type 1 Infection

Abstract

ABSTRACT Virus-specific CD8 + T cells play a central role in the control of viral infections, including human immunodeficiency virus type 1 (HIV-1) infection. However, despite the presence of strong and broad HIV-specific CD8 + T-cell responses in chronic HIV-1 infection, these cells progressively lose critical effector functions and fail to clear the infection. Mounting evidence suggests that the upregulation of several inhibitory regulatory receptors on the surface of CD8 + T cells during HIV-1 infection may contribute directly to the impairment of T-cell function. Here, we investigated the role of killer immunoglobulin receptors (KIR), which are expressed on NK cells and on CD8 + T cells, in regulating CD8 + T-cell function in HIV-1 infection. KIR expression was progressively upregulated on CD8 + T cells during HIV-1 infection and correlated with the level of viral replication. Expression of KIR was associated with a profound inhibition of cytokine secretion, degranulation, proliferation, and activation by CD8 + T cells following stimulation with T-cell receptor (TCR)-dependent stimuli. In contrast, KIR + CD8 + T cells responded potently to TCR-independent stimulation, demonstrating that these cells are functionally competent. KIR-associated suppression of CD8 + T-cell function was independent of ligand engagement, suggesting that these regulatory receptors may constitutively repress TCR activation. This ligand-independent repression of TCR activation of KIR + CD8 + T cells may represent a significant barrier to therapeutic interventions aimed at improving the quality of the HIV-specific CD8 + T-cell response in infected individuals.