Activation of natural regulatory T cells by IgG Fc-derived peptide "Tregitopes"

被引:324
作者
De Groot, Anne S. [1 ,2 ]
Moise, Leonard [1 ]
McMurry, Julie A. [1 ]
Wambre, Erik [3 ]
Van Overtvelt, Laurence [3 ]
Moingeon, Philippe [3 ]
Scott, David W. [4 ]
Martin, William [1 ]
机构
[1] EpiVax, Providence, RI 02903 USA
[2] Univ Rhode Isl, Providence, RI 02908 USA
[3] Stallergenes, Antony, France
[4] Univ Maryland, Baltimore, MD 21201 USA
关键词
D O I
10.1182/blood-2008-02-138073
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We have identified at least 2 highly promiscuous major histocompatibility complex class II T-cell epitopes in the Fc fragment of IgG that are capable of specifically activating CD4(+)CD25(Hi)FoxP3(+) natural regulatory T cells (nT(Regs)). Coincubation of these regulatory T-cell epitopes or "Tregitopes" and antigens with peripheral blood mononuclear cells led to a suppression of effector cytokine secretion, reduced proliferation of effector T cells, and caused an increase in cell surface markers associated with T-Regs such as FoxP3. In vivo administration of the murine homologue of the Fc region Tregitope resulted in suppression of immune response to a known immunogen. These data suggest that one mechanism for the immunosuppressive activity of IgG, such as with IVIG, may be related to the activity of regulatory T cells. In this model, regulatory T-cell epitopes in IgG activate a subset of nTRegs that tips the resulting immune response toward tolerance rather than immunogenicity.
引用
收藏
页码:3303 / 3311
页数:9
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