Cellular and Molecular Life Sciences CMLS

, Volume 58, Issue 1, pp 4–43

The CD40/CD154 receptor/ligand dyadRID="†"ID="†" Review

  • U. Schönbeck*RID="*"ID="*" Corresponding author.
  • P. Libby

DOI: 10.1007/PL00000776

Cite this article as:
Schönbeck*RID="*"ID="*" Corresponding author., U. & Libby, P. CMLS, Cell. Mol. Life Sci. (2001) 58: 4. doi:10.1007/PL00000776


Until recently, the expression and primary function of the cell surface receptor CD40 and its ligand CD154 were considered restricted to B and T lymphocytes, and their interactions required for the thymus-dependent humoral response. However, current work from several groups challenges this view of the CD40/CD154 dyad as a mere mediator of lymphocyte communication. A variety of non-lymphocytic cell types express both receptor and ligand, including hematopoetic and non-hematopoetic cells, such as monocytes, basophils, eosinophils, dendritic cells, fibroblasts, smooth muscle, and endothelial cells. Accordingly, ligation of CD40 mediates a broad variety of immune and inflammatory responses, such as the expression of adhesion molecules, cytokines, matrix-degrading enzymes, prothrombotic activities, and apoptotic mediators. Consequently, CD40 signaling has been associated with pathogenic processes of chronic inflammatory diseases, such as autoimmune diseases, neurodegenerative disorders, graft-versus-host disease, cancer, and atherosclerosis. This review focuses on the synthesis and structure of CD40 and outlines CD154/CD40 signaling pathways, and emphasizes the previously unexpected importance of the CD40/CD154 receptor/ligand dyad in a spectrum of immunoregulatory processes and prevalent human diseases.

Key words. CD154; CD40; immunity; inflammation; arteriosclerosis. 

Copyright information

© Birkhäuser Verlag Basel, 2001

Authors and Affiliations

  • U. Schönbeck*RID="*"ID="*" Corresponding author.
    • 1
  • P. Libby
    • 1
  1. 1.Cardiovascular Medicine, Department of Medicine, Brigham & Women's Hospital and Harvard Medical School, 221 Longwood Ave., LMRC 307, Boston (Massachusetts 02115, USA), Fax +1 617 732 6961, e-mail: uschoenbeck@rics.bwk.harward.edu US

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