Prevention of diabetes in nonobese diabetic mice mediated by CD1d-restricted nonclassical NKT cells

被引:90
|
作者
Duarte, N
Stenström, M
Campino, S
Bergman, ML
Lundholm, M
Holmberg, D
Cardell, SL [1 ]
机构
[1] Lund Univ, Ctr Biomed I13, Immunol Sect, S-22184 Lund, Sweden
[2] Umea Univ, Dept Med Biosci Med & Clin Genet, Umea, Sweden
[3] Gulbenkian Inst Sci, Oeiras, Portugal
[4] Norrland Univ Hosp, Dept Clin Genet, Umea, Sweden
来源
JOURNAL OF IMMUNOLOGY | 2004年 / 173卷 / 05期
关键词
D O I
10.4049/jimmunol.173.5.3112
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A role for regulatory lymphocytes has been demonstrated in the pathogenesis of type I diabetes in the NOD mouse but the nature of these cells is debated. CD1d-restricted NKT lymphocytes have been implicated in this process. Previous reports of reduced diabetes incidence in NOD mice in which the numbers of NKT cells are artificially increased have been attributed to the enhanced production of IL-4 by these cells and a role for classical NKT cells, using the Valpha14-Jalpha18 rearrangement. We now show that overexpression in NOD mice of CD1d-restricted TCR Valpha3.2(+)Vbeta9(+) NKT cells producing high levels of IFN-gamma but low amounts of IL-4 leads to prevention of type 1 diabetes, demonstrating a role for nonclassical CD1d-restricted NKT cells in the regulation of autoimmune diabetes.
引用
收藏
页码:3112 / 3118
页数:7
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