TY - JOUR
T1 - Beneficial Effect of Tolerogenic Dendritic Cells Pulsed with MOG Autoantigen in Experimental Autoimmune Encephalomyelitis
AU - Mansilla, María José
AU - Sellès-Moreno, Carla
AU - Fàbregas-Puig, Sara
AU - Amoedo, Joan
AU - Navarro-Barriuso, Juan
AU - Teniente-Serra, Aina
AU - Grau-López, Laia
AU - Ramo-Tello, Cristina
AU - Martínez-Cáceres, Eva M.
PY - 2015/1/1
Y1 - 2015/1/1
N2 - © 2014 John Wiley & Sons Ltd. Summary: Background: Treatment with tolerogenic dendritic cells (TolDC) is a promising, cell-based strategy to regulate autoimmune diseases such as multiple sclerosis (MS) in an antigen-specific way. This technique involves the use of TolDC from MS patients cultured in the presence of vitamin D3 (VitD3) and pulsed with myelin peptides to induce a stable hyporesponsiveness in myelin-specific autologous T cells. Aim: The purpose of this study was to analyze the in vivo effect of VitD3-TolDC treatment on experimental autoimmune encephalomyelitis, an animal model of MS. Methods: Bone marrow-derived TolDC cultured in the presence of VitD3 and pulsed with peptide 40-55 of the myelin oligodendrocyte glycoprotein (MOG40-55) were administrated preventively, preclinically, and therapeutically to EAE-induced mice. Results: We found that VitD3-TolDC-MOG treatment showed a beneficial effect, not only decreasing the incidence of the disease but also reducing the severity of the clinical signs mediated by induction of regulatory T cells (Treg), as well as IL-10 production and reduction of Ag-specific lymphoproliferation. Our results support VitD3-TolDC-peptide(s) treatment as a potential strategy to restore tolerance in autoimmune diseases such as MS.
AB - © 2014 John Wiley & Sons Ltd. Summary: Background: Treatment with tolerogenic dendritic cells (TolDC) is a promising, cell-based strategy to regulate autoimmune diseases such as multiple sclerosis (MS) in an antigen-specific way. This technique involves the use of TolDC from MS patients cultured in the presence of vitamin D3 (VitD3) and pulsed with myelin peptides to induce a stable hyporesponsiveness in myelin-specific autologous T cells. Aim: The purpose of this study was to analyze the in vivo effect of VitD3-TolDC treatment on experimental autoimmune encephalomyelitis, an animal model of MS. Methods: Bone marrow-derived TolDC cultured in the presence of VitD3 and pulsed with peptide 40-55 of the myelin oligodendrocyte glycoprotein (MOG40-55) were administrated preventively, preclinically, and therapeutically to EAE-induced mice. Results: We found that VitD3-TolDC-MOG treatment showed a beneficial effect, not only decreasing the incidence of the disease but also reducing the severity of the clinical signs mediated by induction of regulatory T cells (Treg), as well as IL-10 production and reduction of Ag-specific lymphoproliferation. Our results support VitD3-TolDC-peptide(s) treatment as a potential strategy to restore tolerance in autoimmune diseases such as MS.
KW - Dendritic cells
KW - Experimental autoimmune encephalomyelitis
KW - Regulatory T cells
KW - Tolerance
KW - Vitamin D 3
U2 - 10.1111/cns.12342
DO - 10.1111/cns.12342
M3 - Article
SN - 1755-5930
VL - 21
SP - 222
EP - 230
JO - CNS Neuroscience and Therapeutics
JF - CNS Neuroscience and Therapeutics
IS - 3
ER -