The Extracellular Domain of CD83 Inhibits Dendritic Cell–mediated T Cell Stimulation and Binds to a Ligand on Dendritic Cells

Author:

Lechmann Matthias1,Krooshoop Daniëlle J.E.B.2,Dudziak Diana3,Kremmer Elisabeth34,Kuhnt Christine1,Figdor Carl G.2,Schuler Gerold1,Steinkasserer Alexander1

Affiliation:

1. Department of Dermatology, University of Erlangen-Nuremberg, D-91052 Erlangen, Germany

2. Department of Tumor Immunology, NCMLS/187 Til, University Medical Center, 6500HB Nijmegen, Netherlands

3. Institute of Clinical Molecular Biology and Tumor Genetik, GSF-Forschungszentrum fur Umwelt und Gesundheit, GmbH, D-81377 Munich, Germany

4. Institute of Molecular Immunology, GSF-Forschungszentrum fur Umwelt und Gesundheit, GmbH, D-81377 Munich, Germany

Abstract

CD83 is an immunoglobulin (Ig) superfamily member that is upregulated during the maturation of dendritic cells (DCs). It has been widely used as a marker for mature DCs, but its function is still unknown. To approach its potential functional role, we have expressed the extracellular Ig domain of human CD83 (hCD83ext) as a soluble protein. Using this tool we could show that immature as well as mature DCs bind to CD83. Since CD83 binds a ligand also expressed on immature DCs, which do not express CD83, indicates that binding is not a homophilic interaction. In addition we demonstrate that hCD83ext interferes with DC maturation downmodulating the expression of CD80 and CD83, while no phenotypical effects were observed on T cells. Finally, we show that hCD83ext inhibits DC-dependent allogeneic and peptide-specific T cell proliferation in a concentration dependent manner in vitro. This is the first report regarding functional aspects of CD83 and the binding of CD83 to DCs.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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