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Updated: Sep 28, 2026

Development and Functional Characterization of Murine Tolerogenic Dendritic Cells
Published on: May 18, 2018
Role of CD83 in the immunomodulation of dendritic cells
Matthias Lechmann1, Elisabeth Zinser, Antje Golka
1Department of Dermatology, University of Erlangen-Nürnberg, Erlangen, Germany.
Insights
Glycoprotein CD83 is crucial for dendritic cell (DC) maturation and immune responses. Studies show CD83 plays key roles in T cell proliferation and generation, highlighting its immunomodulatory functions.
Area of Science:
- Immunology
- Cell Biology
Background:
- Glycoprotein CD83 is a well-established marker for human dendritic cell (DC) maturation.
- Its upregulation with co-stimulatory molecules (CD80, CD86) suggests a role in immune response induction.
Purpose of the Study:
- To investigate the functional role of CD83 in dendritic cell biology and immune responses.
- To elucidate the immunostimulatory and regulatory effects of CD83.
Main Methods:
- Utilizing infection studies with herpes simplex virus type 1 (HSV-1).
- Investigating CD83 mRNA nuclear-to-cytoplasmic transport inhibition.
- Employing a soluble form of the extracellular CD83 domain to inhibit DC-mediated T cell proliferation.
- Analyzing CD83-/- knockout mice to assess T cell generation.
Main Results:
- A soluble CD83 domain completely inhibited DC-mediated T cell proliferation.
- CD83 exhibits both immunostimulatory and regulatory effects.
- CD83-/- knockout mice showed a block in CD4+ T cell generation.
Conclusions:
- CD83 is essential for DC biology and plays a significant role in T cell responses.
- CD83 possesses novel immunomodulatory functions, impacting T cell generation.
Abstract:
Glycoprotein CD83 is one of the best-known maturation markers for human dendritic cells (DCs). The fact that CD83 is strongly upregulated together with co-stimulatory molecules such as CD80 and CD86 during DC maturation suggests it plays an important role in the induction of immune responses. Infection studies with herpes simplex virus type 1 (HSV-1) and the inhibition of the CD83 mRNA specific transport from the nucleus to the cytoplasm suggested a possible functional role for CD83. The first clear proof that CD83 is indeed important for DC biology came from recently performed studies using a soluble form of the extracellular CD83 domain. DC-mediated T cell proliferation could be completely inhibited using this recombinant molecule. Additional studies elucidated immunostimulatory as well as regulatory effects of the CD83 molecule. Furthermore, CD83-/- knockout mice revealed a block in CD4+ T cell generation, a new possible immunomodulatory function of CD83.
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