Abstract
Multiple sclerosis (MS) is an autoimmune disorder directed against self antigens of the central nervous system. CD4+CD25+FoxP3+ regulatory T cell (Treg) mediated suppression is an essential mechanism of self-tolerance. We studied whether changes in the suppressive function of a mixture of CD25high and CD25intemediate expressing Treg cells in myelin basic protein (MBP)-induced proliferation occurred in untreated MS patients. Suppression of MBP-induced proliferation was observed in 13 out of 29 (45%) MS patients; this was significantly (p < 0.05) less compared with 17 out of 19 (89%) healthy individuals. Relative Treg counts was significantly increased in MS patients (mean ± S.D.; 20 ± 8%) compared with healthy individuals (15 ± 5%). These findings suggest that impaired Treg function may be involved in pathogenesis of MS. © 2006 Elsevier B.V. All rights reserved.
Author supplied keywords
Cite
CITATION STYLE
Kumar, M., Putzki, N., Limmroth, V., Remus, R., Lindemann, M., Knop, D., … Grosse-Wilde, H. (2006). CD4+CD25+FoxP3+ T lymphocytes fail to suppress myelin basic protein-induced proliferation in patients with multiple sclerosis. Journal of Neuroimmunology, 180(1–2), 178–184. https://doi.org/10.1016/j.jneuroim.2006.08.003
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.