Proceedings of the National Academy of Sciences · 1997 · 103 citations · 24 references
Life SciencesImmunologyInfectious DiseasesCellular ImmunologyImmunology Of Infectious DiseasesImmunoregulationCell-mediated ImmunityCytotoxic T Lymphocyte ResponsesNatural Killer Cell BiologyNatural Killer Cell FunctionT Cell ActivationT Cell BiologyCytotoxic T Lymphocyte FunctionInhibitory Killer Cell Immunoglobulin-like ReceptorsNatural Killer Cell Inhibitory Receptor RegulationNatural Killer Cell Inhibitory SignalingT-cell Immune ResponsesViral-specific Cytotoxic T Lymphocyte Responses
Human T lymphocytes have been shown to express inhibitory natural killer cell receptors (NKR), which can down-regulate T cell antigen receptor-mediated T cell function, including cytolytic activity. In the present study, we demonstrate that CD3+NKR+ cells can be identified in HIV-infected patients. HIV-specific cytolytic activity was analyzed in five patients in whom autologous lymphoblastoid B cell lines could be derived as a source of autologous target cells. Phytohemagglutinin-activated T cell populations that had been cultured in interleukin 2 displayed HIV-specific cytotoxic T lymphocyte (CTL) activity against HIV env, gag, pol, and nef in 3 of 5 patients. Addition of anti-NKR mAb of IgM isotype could increase the specific CTL activity. Moreover, in one additional patient, HIV-specific CTL activity was undetectable; however, after addition of anti-NKR mAb such CTL activity appeared de novo. Similar results were obtained by analysis of CD3+NKR+ clones derived from two patients. These data provide direct evidence that CD3+NKR+ cells may include antigen (HIV)-specific CTLs and that mAb-mediated masking of inhibitory NKR may revert the down-regulation of CTL function.
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Alessandro Moretta, Cristina Bottino, Daniela Pende et al. · The Journal of Experimental Medicine · 1990 · 379 citations · Full text