Naive B cells generate regulatory T cells in the presence of a mature immunologic synapse

被引:141
作者
Reichardt, Peter
Dornbach, Bastian
Rong, Song
Beissert, Stefan
Gueler, Faikah
Loser, Karin
Gunzer, Matthias
机构
[1] Helmholtz Ctr Infect Res, Jr Res Grp Immunodynam, D-38124 Braunschweig, Germany
[2] Hannover Med Sch, Dept Nephrol, D-3000 Hannover, Germany
[3] Univ Munster, Dept Dermatol, D-4400 Munster, Germany
[4] Univ Munster, IZKF, D-4400 Munster, Germany
关键词
PROTEIN-KINASE-C; DENDRITIC CELLS; IN-VIVO; ANTIGEN PRESENTATION; L-SELECTIN; RECEPTOR MICROCLUSTERS; HOMING RECEPTORS; IMMUNE SYNAPSE; TOLERANCE; EXPRESSION;
D O I
10.1182/blood-2006-10-053793
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Naive B cells are ineffective antigen presenting cells and are considered unable to activate naive T cells. However, antigen-specific contact of these cells leads to stable cell pairs that remain associated over hours in vivo. The physiologic role of such pairs has not been evaluated. We show here that antigen-specific conjugates between naive B cells and naive T cells display a mature immunologic synapse in the contact zone that is absent in T-cell-dendritic cell (DC) pairs. B cells induce substantial proliferation but, contrary to DCs, no loss of L-selectin in T cells. Surprisingly, while DC-triggered T cells develop into normal effector cells, B-cell stimulation over 72 hours induces regulatory T cells inhibiting priming of fresh T cells in a contact-dependent manner in vitro. In vivo, the regulatory T cells home to lymph nodes where they potently suppress immune responses such as in cutaneous hypersensitivity and ectopic allogeneic heart transplant rejection. Our finding might help to explain old observations on tolerance induction by B cells, identify the mature immunologic synapse as a central functional module of this process, and suggest the use of naive B-cell-primed regulatory T cells, "bTregs," as a useful approach for therapeutic intervention in adverse adaptive immune responses.
引用
收藏
页码:1519 / 1529
页数:11
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