Author/Authors :
Ito، نويسنده , , Atsushi and Buenafe، نويسنده , , Abigail C. and Matejuk، نويسنده , , Agata and Zamora، نويسنده , , Alex and Silverman، نويسنده , , Marc and Dwyer، نويسنده , , Jami and Vandenbark، نويسنده , , Arthur A. and Offner، نويسنده , , Halina، نويسنده ,
Abstract :
Estrogen treatment has been found to have suppressive activity in several models of autoimmunity. To investigate the mechanism of 17β-estradiol (E2) suppression of experimental autoimmune encephalomyelitis, we evaluated E2 effects on TNF-α expression in the central nervous system (CNS) and spleen of C57BL/6 mice immunized with MOG 35-55/CFA. Kinetic analysis demonstrated that E2 treatment drastically decreased the recruitment of total inflammatory cells as well as TNF-α+ macrophages and T cells into the CNS at disease onset. In contrast, E2 had only moderate effects on the relatively high constitutive TNF-α expression by resident CNS microglial cells. E2 treatment also had profound inhibitory effects on expression of TNF-α by splenic CD4+ T cells, including those responsive to MOG 35–55 peptide. We propose that the mechanism of E2 protection may involve both systemic inhibition of TNF-α expression and local (CNS) recruitment of inflammatory cells, with modest effects on TNF-α expression by resident CNS microglial cells.
Keywords :
macrophages , 17?-Estradiol , TNF-? , EAE , CNS , T cells