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Ligation of CD40 on dendritic cells triggers production of high levels of interleukin-12 and enhances T cell stimulatory capacity: T-T help via APC activation.

The Journal of Experimental Medicine · 1996 · Vol. 184(2) · pp. 747–752
Marina CellaDoris ScheideggerKathrin Palmer-LehmannPeter J. L. LaneAntonio LanzavecchiaGottfried Alber

Abstract

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.

Immunotherapy and Immune ResponsesT-cell and B-cell ImmunologyImmune Cell Function and InteractionCD40CD80CD86Cell biologyDendritic cellT cellInterleukin 12Antigen-presenting cellImmunologyBiology

MeSH terms

Antigen-Presenting CellsHistocompatibility Antigens Class IICell AdhesionCells, CulturedDendritic CellsHumansInterferon-gammaLymphocyte CooperationLymphocyte ActivationMembrane GlycoproteinsT-LymphocytesSignal TransductionAntigens, CDB7-1 AntigenInterleukin-12
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