De novo production of antigen-specific suppressor cells in vivo

被引:33
|
作者
Kretschmer, Karsten [1 ]
Heng, Tracy S. P. [1 ]
von Boehmer, Harald [1 ]
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Pathol, Boston, MA 02115 USA
关键词
D O I
10.1038/nprot.2006.105
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Foxp3-expressing regulatory T cells (T-reg) play an essential role in maintaining tolerance to self antigens and are generated under physiological conditions when developing T cells encounter antigens expressed by thymic epithelial cells. We have addressed the possibility that T-reg can be exploited to prevent or even suppress ongoing immune responses to foreign antigens. To this end, one must develop methods that permit the de novo generation of T-reg specific for foreign antigens in peripheral lymphoid tissue. This report describes the methodology of generating T-reg by delivering minute doses of peptide contained in fusion Abs directed against the DEC-205 endocytic receptor on steady-state dendritic cells. The process, from cloning and production of fusion Abs to antigen-specific T-reg induction in vivo, takes similar to 2 months. The results show that delivery of T-cell receptor agonist ligands under subimmunogenic conditions represents a suitable approach for converting naive T cells into T-reg.
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页码:653 / 661
页数:9
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