| Literature DB >> 23778260 |
Bruna Teixeira1, Vera Carolina B Bittencourt, Thais B Ferreira, Taissa M Kasahara, Priscila O Barros, Regina Alvarenga, Joana Hygino, Regis M Andrade, Arnaldo F Andrade, Cleonice A M Bento.
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.Entities:
Keywords: CD8(+) T cells; Cytokines;; IL-10;; Lipopolysaccharide;; Multiple sclerosis;; Th17;
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Year: 2013 PMID: 23778260 DOI: 10.1016/j.clim.2013.05.012
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969