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

被引:0
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作者
Katharina Aschenbrenner
Louise M D'Cruz
Elisabeth H Vollmann
Maria Hinterberger
Jan Emmerich
Lee Kim Swee
Antonius Rolink
Ludger Klein
机构
[1] Research Institute of Molecular Pathology,Department of Clinical and Biological Sciences
[2] Center for Biomedicine,undefined
[3] University of Basel,undefined
[4] Present addresses: Division of Biological Sciences,undefined
[5] University of California,undefined
[6] San Diego,undefined
[7] La Jolla,undefined
[8] California 92093,undefined
[9] USA (L.M.D.) and The CBR Institute for Biomedical Research,undefined
[10] Department of Pathology,undefined
[11] Brigham and Women's Hospital,undefined
[12] Harvard Medical School,undefined
[13] Boston,undefined
[14] Massachusetts 02115,undefined
[15] USA (E.H.V.).,undefined
来源
Nature Immunology | 2007年 / 8卷
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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.
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页码:351 / 358
页数:7
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