共 23 条
De novo production of antigen-specific suppressor cells in vivo
被引:33
作者:

Kretschmer, Karsten
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机构:
Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Pathol, Boston, MA 02115 USA Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Pathol, Boston, MA 02115 USA

Heng, Tracy S. P.
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Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Pathol, Boston, MA 02115 USA Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Pathol, Boston, MA 02115 USA

von Boehmer, Harald
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机构:
Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Pathol, Boston, MA 02115 USA Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Pathol, Boston, MA 02115 USA
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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