Alloantigen-presenting plasmacytoid dendritic cells mediate tolerance to vascularized grafts

被引:507
作者
Ochando, Jordi C. [1 ]
Homma, Chiho
Yang, Yu
Hidalgo, Andres
Garin, Alexandre
Tacke, Frank
Angeli, Veronique
Li, Yansui
Boros, Peter
Ding, Yaozhong
Jessberger, Rolf
Trinchieri, Giorgio
Lira, Sergio A.
Randolph, Gwendalyn J.
Bromberg, Jonathan S.
机构
[1] CUNY Mt Sinai Sch Med, Dept Gene & Cell Med, New York, NY 10029 USA
[2] CUNY Mt Sinai Sch Med, Hematol Ctr, New York, NY 10029 USA
[3] CUNY Mt Sinai Sch Med, Immunobiol Ctr, New York, NY 10029 USA
[4] CUNY Mt Sinai Sch Med, Recanati Miller Transplantat Inst, New York, NY 10029 USA
[5] Dresden Univ Technol, Dept Physiol Chem, D-8027 Dresden, Germany
[6] NIAID, Parasit Dis Lab, Bethesda, MD 20892 USA
[7] CUNY Mt Sinai Sch Med, Dept Surg, New York, NY 10029 USA
关键词
D O I
10.1038/ni1333
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The induction of alloantigen-specific unresponsiveness remains an elusive goal in organ transplantation. Here we identify plasmacytoid dendritic cells (pDCs) as phagocytic antigen-presenting cells essential for tolerance to vascularized cardiac allografts. Tolerizing pDCs acquired alloantigen in the allograft and then moved through the blood to home to peripheral lymph nodes. In the lymph node, alloantigen-presenting pDCs induced the generation of CCR4(+)CD4(+)CD25(+)Foxp3(+) regulatory T cells (T-reg cells). Depletion of pDCs or prevention of pDC lymph node homing inhibited peripheral Treg cell development and tolerance induction, whereas adoptive transfer of tolerized pDCs induced Treg cell development and prolonged graft survival. Thus, alloantigen-presenting pDCs home to the lymph nodes in tolerogenic conditions, where they mediate alloantigen-specific Treg cell development and allograft tolerance.
引用
收藏
页码:652 / 662
页数:11
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