PubMed · 1999 · 18 citations · 0 references
Life SciencesCell BiologyImmunologyCellular ImmunologyImmunoregulationSignal TransductionCytotoxic T Lymphocyte ResponsesEffector T Cell FunctionLymphocyte ActivationNatural Killer Cell RegulationT Cell ActivationT Cell BiologyActivationAllogeneic T Cell ActivationCd8 Positive T CellsCd8 T Cell ActivationMixed Lymphocyte ReactionNkg2 Receptor SignalingTransforming Growth Factor Beta ReceptorsTransforming Growth Factor-beta Signaling
We have examined the influence of the immunosuppressive cytokine TGF-beta on NK receptor expression by T lymphocytes upon allogeneic activation. Using the primary mixed lymphocyte reaction (MLR), our data show that allostimulation induced the expression of CD94/NKG2-A on alloactivated CD8+ T cells. This expression was increased in the presence of TGF-beta whereas IL-15 had no significant effect. The blockage of CD94 and NKG2-A resulted in increased lysis of targets by alloactivated cytotoxic T cells. This increase was dependent on the activation state of T cells. Using PCR, we also demonstrated that TGF-beta had no effect on the transcription of non-inhibitory NKG2 molecules. The present results show that allostimulation can induce CD94 and further point out the role of TGF-beta in the induction of the CD94/NKG2-A receptor on alloactivated T cells.