TY - JOUR
T1 - Plasmacytoid dendritic cells prime IFN-γ-secreting melanoma-specific CD8 lymphocytes and are found in primary melanoma lesions
AU - Salio, Mariolina
AU - Cella, Marina
AU - Vermi, William
AU - Faccheti, Fabio
AU - Palmowski, Michael J.
AU - Smith, Caroline L.
AU - Shepherd, Dawn
AU - Colonna, Marco
AU - Cerundolo, Vincenzo
N1 - Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2003/4/1
Y1 - 2003/4/1
N2 - 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.
AB - 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.
KW - Melan-A
KW - Plasmacytoid dendritic cell
KW - Priming
KW - Tetramer
KW - Tumor immunity
UR - http://www.scopus.com/inward/record.url?scp=0038744443&partnerID=8YFLogxK
U2 - 10.1002/eji.200323676
DO - 10.1002/eji.200323676
M3 - Review article
C2 - 12672071
AN - SCOPUS:0038744443
SN - 0014-2980
VL - 33
SP - 1052
EP - 1062
JO - European Journal of Immunology
JF - European Journal of Immunology
IS - 4
ER -