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Abstract
Annual Review of Immunology
Vol. 16: 111-135 (Volume publication date April 1998)
(doi:10.1146/annurev.immunol.16.1.111)
CD40 AND CD154 IN CELL-MEDIATED IMMUNITY

Iqbal S. Grewal and Richard A. Flavell*
*Howard Hughes Medical Institute, and Section of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06520; e-mail:

Abstract CD40-CD154–mediated contact-dependent signals between B and T cells are required for the generation of thymus dependent (TD) humoral immune responses. CD40-CD154 interactions are however also important in many other cell systems. CD40 is expressed by a large variety of cell types other than B cells, and these include dendritic cells, follicular dendritic cells, monocytes, macrophages, mast cells, fibroblasts, and endothelial cells. CD40- and CD154-knockout mice and antibodies to CD40 and CD154 have helped to elucidate the role of the CD40-CD154 system in immune responses. Recently published studies indicate that CD40-CD154 interactions can influence T cell priming and T cell–mediated effector functions; they can also upregulate costimulatory molecules and activate macrophages, NK cells, and endothelia as well as participate in organ-specific autoimmune disease, graft rejection, and even atherosclerosis. This review focuses on the role of the CD40-CD154 system in the regulation of many newly discovered functions important in inflammation and cell-mediated immunity.

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Authors:
Iqbal S. Grewal and
Richard A. Flavell
Keywords:
CD40L
T cell activation
T cell priming
T cell effector functions
autoimmunity
parasitic infections

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