CD4+CD25+FoxP3+ T lymphocytes fail to suppress myelin basic protein-induced proliferation in patients with multiple sclerosis

被引:116
作者
Kumar, Manoj
Putzki, Norman
Limmroth, Volker
Remus, Ralph
Lindemann, Monika
Knop, Dietmar
Mueller, Norbert
Hardt, Cornelia
Kreuzfelder, Ernst
Grosse-Wilde, Hans
机构
[1] Univ Klinikum Essen, Inst Transfusmed, D-45122 Essen, Germany
[2] MS Zentrum, Neurol Klin, Essen, Germany
关键词
multiple sclerosis; myelin basic protein; proliferation; regulatory T cells; FOXP3; OLIGODENDROCYTE GLYCOPROTEIN; AUTOIMMUNE-DISEASE; REGULATORY CELLS; TOLERANCE; DIAGNOSIS; SELF;
D O I
10.1016/j.jneuroim.2006.08.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Multiple sclerosis (MS) is an autoimmune disorder directed against self antigens of the central nervous system. CD4(+)CD25(+)FoxP3(+) regulatory T cell (T-reg) mediated suppression is an essential mechanism of self-tolerance. We studied whether changes in the suppressive function of a mixture of CD25(high) and CD25(intermediate) expressing T-reg 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 T-reg counts was significantly increased in MS patients (mean +/- S.D.; 20 +/- 8%) compared with healthy individuals (15 +/- 5%). These findings suggest that impaired T-reg function may be involved in pathogenesis of MS. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:178 / 184
页数:7
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