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.

Marina Cella(Institute of Molecular and Clinical Ophthalmology Basel), Doris Scheidegger(Institute of Molecular and Clinical Ophthalmology Basel), Kathrin Palmer-Lehmann(Institute of Molecular and Clinical Ophthalmology Basel), Peter J. L. Lane(Institute of Molecular and Clinical Ophthalmology Basel), Antonio Lanzavecchia(Institute of Molecular and Clinical Ophthalmology Basel), Gottfried Alber(Institute of Molecular and Clinical Ophthalmology Basel)
The Journal of Experimental Medicine
August 1, 1996
Cited by 1,992Open Access
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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.


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