The Journal of Immunology · 2008 · 34 citations · 39 references
Life SciencesImmunologyInfectious DiseasesCellular ImmunologyImmunopathologyImmunoregulationCell-mediated ImmunityCellular Immunity In InfectionEffector T Cell FunctionImmune DysfunctionImmune SuppressionT Cell BiologyCd8 Positive T CellsCell-mediated Immune DysfunctionCytokine-mediated SuppressionHiv-associated ImmunosuppressionInterleukin-10 Mediated ImmunosuppressionPd-1 SignalingProgrammed Cell Death PathwaysT-cell Immune Responses
Mechanisms leading to the observed immune dysregulation in HIV-1 infection are not well understood. HIV-specific IL-10-positive CD8(+) T cells are increased in advanced HIV disease. We have previously reported that Gag-specific IL-10-positive CD8(+) T cells suppressed cytolysis. In this study we describe the suppressive effect of Nef-specific IL-10-positive CD8(+) T cells. Interestingly, simultaneous removal of both Gag- and Nef-specific IL-10-positive CD8(+) T cells led to higher HIV-specific cytolysis compared with the removal of Nef-specific IL-10-positive CD8(+) T cells alone. We also examined the level of programmed cell death-1 (PD-1) as a measure of immune dysfunction in association with IL-10-positive suppressor CD8(+) T cells. The level of PD-1 expression on CD107-positive effector CD8(+) T cells was significantly increased when IL-10-positive suppressor CD8(+) T cells were present (p < 0.05). Our results suggest that IL-10-positive suppressor CD8(+) T cells contribute to the immune dysfunction observed in advanced HIV infection and that the concomitant presence of multiple IL-10-positive CD8(+) T cell populations may have an additive suppressive effect.
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WanJun Chen, Wenwen Jin, Neil J. Hardegen et al. · The Journal of Experimental Medicine · 2003 · 4.6K citations · Full text