共 125 条
Guarding the immune system:: Suppression of autoimmunity by CD4+CD25+ immunoregulatory T cells
被引:23
作者:

Zwar, Tricia D.
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h-index: 0
机构: Univ Melbourne, Mol Sci & Biotechnol Inst Bio21, Dept Biochem & Mol Biol, Parkville, Vic 3010, Australia

Van Driel, Ian R.
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h-index: 0
机构: Univ Melbourne, Mol Sci & Biotechnol Inst Bio21, Dept Biochem & Mol Biol, Parkville, Vic 3010, Australia

Gleeson, Paul A.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Melbourne, Mol Sci & Biotechnol Inst Bio21, Dept Biochem & Mol Biol, Parkville, Vic 3010, Australia Univ Melbourne, Mol Sci & Biotechnol Inst Bio21, Dept Biochem & Mol Biol, Parkville, Vic 3010, Australia
机构:
[1] Univ Melbourne, Mol Sci & Biotechnol Inst Bio21, Dept Biochem & Mol Biol, Parkville, Vic 3010, Australia
[2] Univ Melbourne, Dept Biochem & Mol Biol, Parkville, Vic 3010, Australia
关键词:
autoimmunity;
rodent;
suppression;
T cell;
T regulatory cell;
D O I:
10.1111/j.1440-1711.2006.01471.x
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
CD4(+)CD25(+)Foxp3(+) T cells (CD25(+) T regulatory [Treg] cells) are a naturally occurring suppressor T-cell population that regulates a wide variety of immune responses. A major function of CD25(+) Treg cells is to inhibit the activity of self-reactive T cells that can potentially cause autoimmune disease. This review examines the recent advances in CD25(+) Treg cell biology, with particular focus on the thymic and peripheral development of CD25(+) Treg cells, the signals that promote their expansion and maintenance in the periphery and the mechanism by which they mediate their suppressor activity in peripheral lymphoid tissues. An understanding of these issues is likely to facilitate the development of CD25(+) Treg-cell-based therapies for the treatment of autoimmune disease.
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页码:487 / 501
页数:15
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