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Plasmacytoid Dendritic cells respond Directly to apoptotic cells by secreting immune regulatory IL-10 or IFN-α
被引:11
|作者:
Simpson, Joanne
[1
]
Miles, Katherine
[1
]
Trub, Marta
[1
]
MacMahon, Roisin
[1
]
Gray, Mohini
[1
]
机构:
[1] Univ Edinburgh, Queens Med Res Inst, MRC, Ctr Inflammat Res, Edinburgh, Midlothian, Scotland
来源:
FRONTIERS IN IMMUNOLOGY
|
2016年
/
7卷
基金:
英国惠康基金;
英国医学研究理事会;
关键词:
plasmacytoid dendritic cell;
apoptotic cell;
apoptosis;
toll-like receptor;
IL-10;
SYSTEMIC-LUPUS-ERYTHEMATOSUS;
DRAINING LYMPH-NODES;
TOLL-LIKE RECEPTORS;
HUMAN B-CELLS;
INDOLEAMINE 2,3-DIOXYGENASE;
AUTOANTIBODY PRODUCTION;
MURINE LUPUS;
SELF-DNA;
T-CELLS;
INDUCTION;
D O I:
10.3389/fimmu.2016.00590
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Plasmacytoid dendritic cells (pDCs) play a pivotal role in driving the autoimmune disease systemic lupus erythematosus, via the secretion of IFN-alpha in response to nuclear self-antigens complexed with autoantibodies. Apoptotic cells, generated at sites of inflammation or secondary lymphoid organs, are exposed to activated pDCs and also express the same nuclear antigens on their cell surface. Here, we show that in the absence of autoantibodies, activated pDCs directly respond to apoptotic cell-expressed chromatin complexes by secreting IL-10 and IL-6, which also induces T cells to secrete IL-10. Conversely, when activated by the viral mimetic CpG-A, apoptotic cells enhance their secretion of IFN-alpha. This study demonstrates that activated pDCs respond directly to apoptotic cells and may maintain tolerance via IL-10, or promote inflammation through secretion of IFN-alpha, depending on the inflammatory context.
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页数:13
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