Selection of Foxp3+ regulatory T cells specific for self antigen expressed and presented by Aire+ medullary thymic epithelial cells

被引:460
作者
Aschenbrenner, Katharina
D'Cruz, Louise M.
Vollmann, Elisabeth H.
Hinterberger, Maria
Emmerich, Jan
Swee, Lee Kim
Rolink, Antonius
Klein, Ludger
机构
[1] Res Inst Mol Pathol, A-1030 Vienna, Austria
[2] Univ Basel, Dept Clin & Biol Sci, Ctr Biomed, CH-4051 Basel, Switzerland
[3] Harvard Univ, CBR Inst Biomed Res, Dept Pathol, Brigham & Womens Hosp,Med Sch, Boston, MA 02115 USA
关键词
D O I
10.1038/ni1444
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
The parameters specifying whether autoreactive CD4(+) thymocytes are deleted ( recessive tolerance) or differentiate into regulatory T cells ( dominant tolerance) remain unresolved. Dendritic cells directly delete thymocytes, partly through cross-presentation of peripheral antigens ` promiscuously' expressed in medullary thymic epithelial cells ( mTECs) positive for the autoimmune regulator Aire. It is unclear if and how mTECs themselves act as antigen-presenting cells during tolerance induction. Here we found that an absence of major histocompatibility class II molecules on mTECs resulted in fewer polyclonal regulatory T cells. Furthermore, targeting of a model antigen to Aire(+) mTECs led to the generation of specific regulatory T cells independently of antigen transfer to dendritic cells. Thus, 'routing' of mTEC-derived self antigens may determine whether specific thymocytes are deleted or enter the regulatory T cell lineage.
引用
收藏
页码:351 / 358
页数:8
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