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CD4+CD25+ T regulatory cells in murine pregnancy
被引:70
|作者:
Zenclussen, AC
[1
]
机构:
[1] Med Univ Berlin, Inst Med Immunol, Biomed Forschungszentrum, D-13353 Berlin, Germany
关键词:
Treg cells;
Th1/Th2;
pregnancy;
tolerance;
foxp3;
D O I:
10.1016/j.jri.2005.01.003
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
'Mammalian pregnancy is thought to be a state of immunological tolerance and immunological pregnancy complications may result from incomplete allo-tolerance. We reported recently a higher frequency of Th1 cytokine-producing T cells specific against paternal antigens in abortion-prone mice compared to normal pregnant mice. Since Th2 cells were shown to be not essential for normal pregnancy; alloreactive Th1 cells must be differently regulated. In this context, T regulatory cells (Treg) were proposed to play an essential role. Normal pregnant mice show an expansion of CD4(+)CD25(+) and IL-10(+) Treg cells at the periphery compared to nonpregnant animals. Further, we reported significantly lower frequencies of Treg in abortion-prone mice. Interestingly, CD4(+)CD25(+) Treg cells from normal pregnant mice were able to prevent fetal rejection. Accordingly, down-regulated levels of Treg were also reported during human miscarriage. The putative mechanisms involved in Treg-induced tolerance in mice and humans are discussed in this review. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
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页码:101 / 110
页数:10
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