The Journal of Experimental Medicine · 1996 · 2K citations · 20 references
Life SciencesCell BiologyImmunologyCell SignalingCellular ImmunologyImmunoregulationCell-mediated ImmunityCytokine BiologyDendritic Cell BiologyDendritic Cell RegulationT Cell ActivationT Cell BiologyCd40l SignalingCd86 InteractionsDendritic Cell Cytokine ProductionDendritic Cell-mediated T Cell ActivationDendritic Cell-t Cell InteractionInterferon Gamma ProductionT Helper Cell CytokinesT Helper Cell Effector Functions
We investigated the possibility that T helper cells might enhance the stimulatory function of dendritic cells (DCs). We found that ligation of CD40 by CD40L triggers the production of extremely high levels of bioactive IL-12. Other stimuli such as microbial agents, TNF-alpha or LPS are much less effective or not at all. In addition, CD40L is the most potent stimulus in upregulating the expression of ICAM-1, CD80, and CD86 molecules on DCs. These effects of CD40 ligation result in an increased capacity of DCs to trigger proliferative responses and IFN-gamma production by T cells. These findings reveal a new role for CD40-CD40L interaction in regulating DC function and are relevant to design therapeutic strategies using cultured DCs.
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