Development and Function of Dendritic Cell Subsets

被引:722
作者
Mildner, Alexander [1 ]
Jung, Steffen [1 ]
机构
[1] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
关键词
CD8(+) T-CELLS; STEADY-STATE CONDITIONS; PERIPHERAL LYMPHOID ORGANS; EPIDERMAL LANGERHANS CELLS; TRANSCRIPTION FACTOR E2-2; BLOOD-BORNE ANTIGENS; MOUSE BONE-MARROW; IN-VIVO; CROSS-PRESENTATION; GM-CSF;
D O I
10.1016/j.immuni.2014.04.016
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Classical dendritic cells (cDCs) form a critical interface between innate and adaptive immunity. As myeloid immune cell sentinels, cDCs are specialized in the sensing of pathogen challenges and cancer. They translate the latter for T cells into peptide form. Moreover, cDCs provide additional critical information on the original antigen context to trigger a diverse spectrum of appropriate protective responses. Here we review recent progress in our understanding of cDC subsets in mice. We will discuss cDC subset ontogeny and transcription factor dependencies, as well as emerging functional specializations within the cDC compartment in lymphoid and nonlymphoid tissues.
引用
收藏
页码:642 / 656
页数:15
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