FoxP3;
regulatory T cells;
migration;
chemokine receptor;
integrin;
selectin;
D O I:
10.1007/s00005-007-0024-8
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
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.