Abstract
Plasmacytoid dendritic cells (PDC) are a small population of leukocytes specialized in the production of type I IFN. It has been shown that PDC have a potent T cell stimulatory capacity in allogeneic mixed lymphocyte reaction, However, their role in initiating primary immune responses remains elusive. We report that blood PDC efficiently prime naive CD8+ lymphocytes specific for the melan-A26-35 epitope to become IFN-γ producing cells in vitro. In addition, we found that CD40L-stimulated PDC induce expression on primed melan-A-specific T cells of cutaneous lymphocyte antigen and L-selectin (CD62L), homing receptors that allow the migration of effector cells to the inflamed skin. Finally, we show that PDC can be found in the peri-tumoral area of most primary cutaneous melanomas in vivo and that type I IFN-containing supernatants derived from PDC increase melanoma cell surface expression of CD95 and MHC class I and class II molecules in vitro. Our results suggest a new immunomodulatory role for tissue infiltrating PDC, which may prime tumor-specific T cell responses and affect tumor growth via soluble factors.
| Original language | English |
|---|---|
| Pages (from-to) | 1052-1062 |
| Number of pages | 11 |
| Journal | European Journal of Immunology |
| Volume | 33 |
| Issue number | 4 |
| DOIs | |
| State | Published - Apr 1 2003 |
Keywords
- Melan-A
- Plasmacytoid dendritic cell
- Priming
- Tetramer
- Tumor immunity
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