Author/Authors :
Teixeira، نويسنده , , Bruna and Bittencourt، نويسنده , , Vera Carolina B. and Ferreira، نويسنده , , Thais B. and Kasahara، نويسنده , , Taissa M. and Barros، نويسنده , , Priscila O. and Alvarenga، نويسنده , , Regina and Hygino، نويسنده , , Joana and Andrade، نويسنده , , Regis M. and Andrade، نويسنده , , Arnaldo F. and Bento، نويسنده , , Cleonice A.M.، نويسنده ,
Abstract :
Exogenous glucocorticoid plays an important role in controlling clinical relapses of multiple sclerosis (MS), but the response to this treatment differs among patients. In this study, T-cell proliferation and IL-17 production were less sensitive to hydrocortisone (HC) inhibition in MS patients than healthy individuals, mainly in CD8+ compartment. Furthermore, in vitro IL-17 production was positively related with neurological disability and its release was proportional to IL-23 and IL-6 productions by LPS-activated monocytes. Interestingly, elevated LPS levels were quantified in the plasma of MS patients, and their levels were directly related to in vivo IL-6 production. Finally, HC-resistance in reducing IL-17 production by polyclonally-activated CD8+ T cells was particularly observed among MS patients with higher in vivo LPS levels. In summary, the results indicate that T-cells derived from MS patients show an enhanced Th17-like phenotype that is directly associated with neurological disability, resistance to glucocorticoid inhibition and elevated bacterial translocation.
Keywords :
CD8+ T cells , IL-10 , Multiple sclerosis , Lipopolysaccharide , cytokines , Th17