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.
MeSH Terms
Antigen-Presenting Cells/immunology
Antigens, CD/metabolism
B7-1 Antigen/metabolism
B7-2 Antigen
CD40 Antigens/physiology
CD40 Ligand
Cell Adhesion
Cells, Cultured
Dendritic Cells/immunology
Fluorescent Antibody Technique, Indirect
Histocompatibility Antigens Class II/metabolism
Humans
Intercellular Adhesion Molecule-1/metabolism
Interferon-gamma/biosynthesis
Interleukin-12/biosynthesis
Lymphocyte Activation
Lymphocyte Cooperation
Membrane Glycoproteins/metabolism,physiology
Signal Transduction
T-Lymphocytes/immunology
Chemicals
Antigens, CD
B7-1 Antigen
B7-2 Antigen
CD40 Antigens
CD86 protein, human
Histocompatibility Antigens Class II
Membrane Glycoproteins
Intercellular Adhesion Molecule-1
CD40 Ligand
Interleukin-12
Interferon-gamma
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Cella M
Basel Institute for Immunology, Switzerland.
Scheidegger D
Palmer-Lehmann K
Lane P
Lanzavecchia A
Alber G
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