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Trafficking of FoxP3+ regulatory T cells: myths and facts
被引:0
|作者:
Chang H. Kim
机构:
[1] Purdue University,Department of Comparative Pathobiology, Purdue Cancer Center, Laboratory of Immunology and Hematopoiesis
来源:
Archivum Immunologiae et Therapiae Experimentalis
|
2007年
/
55卷
关键词:
FoxP3;
regulatory T cells;
migration;
chemokine receptor;
integrin;
selectin;
D O I:
暂无
中图分类号:
学科分类号:
摘要:
Fork head box P3 (FoxP3+) regulatory T cells (Tregs) are specialized T cells for prevention of hyperimmune responses and autoimmunity. Tumors and pathogens can hijack FoxP3+ Tregs to evade host immune responses. There is an increasing body of evidence that trafficking of FoxP3+ Tregs is important for their effective suppression of target cells. Because of their distinctive functions and gene expression phenotype, the migratory behavior of FoxP3+ Tregs has been somewhat mystified. The myths are that they have unique trafficking receptors and migratory behaviors that are different from those of conventional T cells. Another related myth is that FoxP3+ regulatory T cell subsets have a fixed trafficking behavior from the time they are generated in the thymus. The recent progress in trafficking receptors and migratory behavior of FoxP3+ Tregs is reviewed here and the validity of these myths is examined.
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页码:151 / 159
页数:8
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