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CD4+ CD25+ Foxp3+ T Regulatory Cells with Limited TCR Diversity in Control of Autoimmunity
被引:39
作者:
Adeegbe, Dennis
[1
]
Matsutani, Takaii
[1
]
Yang, Jing
[1
]
Altman, Norman H.
[2
]
Malek, Thomas R.
[1
,3
]
机构:
[1] Univ Miami, Dept Microbiol & Immunol, Miller Sch Med, Miami, FL 33101 USA
[2] Univ Miami, Dept Pathol, Miller Sch Med, Miami, FL 33101 USA
[3] Univ Miami, Diabet Res Inst, Miller Sch Med, Miami, FL 33101 USA
基金:
美国国家卫生研究院;
关键词:
RECEPTOR-BETA;
CUTTING EDGE;
REPERTOIRE;
MICE;
SELF;
SELECTION;
ANTIGEN;
INTERLEUKIN-2;
SPECIFICITY;
EXPRESSION;
D O I:
10.4049/jimmunol.0902379
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
The importance of high TCR diversity of T regulatory (Treg) cells for self-tolerance is poorly understood. To address this issue, TCR diversity was measured for Treg cells after transfer into IL-2R beta(-/-) mice, which develop lethal autoimmunity because of failed production of Treg cells. In this study, we show that high TCR diversity of pretransferred Treg cells led to selection of therapeutic Treg cells with lower TCR diversity that prevented autoimmunity. Pretransferred Treg cells with lower diversity led to selection of Treg cells through substantial peripheral reshaping with even more restricted TCR diversity that also suppressed autoimmune symptoms. Thus, in a setting of severe breakdown of immune tolerance because of failed production of Treg cells, control of autoimmunity is achieved by only a fraction of the Treg TCR repertoire, but the risk for disease increased. These data support a model in which high Treg TCR diversity is a mechanism to ensure establishing and maintaining self-tolerance. The Journal of Immunology, 2010, 184: 56-66.
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页码:56 / 66
页数:11
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