Functional specializations of human epidermal langerhans cells and CD14+ dermal dendritic cells

被引:479
|
作者
Klechevsky, Eynav [1 ,2 ]
Morita, Rimpei [1 ,2 ]
Liu, Maochang [1 ,2 ]
Cao, Yanying [1 ,2 ]
Coquery, Sebastien [1 ,2 ]
Thompson-Snipes, LuAnn [1 ,2 ]
Briere, Francine [1 ,2 ]
Chaussabel, Damien [1 ,2 ]
Zurawski, Gerard [1 ,2 ]
Palucka, A. Karolina [1 ,2 ]
Reiter, Yoram [3 ]
Banchereau, Jacques [1 ,2 ]
Ueno, Hideki [1 ,2 ]
机构
[1] Baylor Inst Immunol Res, Dallas, TX 75204 USA
[2] Baylor Res Inst, Dallas, TX 75204 USA
[3] Technion Israel Inst Technol, IL-32000 Technion, Haifa, Israel
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.immuni.2008.07.013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Little is known about the functional differences between the human skin myeloid dendritic cell (DC) subsets, epidermal CD207(+) Langerhans cells (LCs) and dermal CD14(+) DCs. We showed that CD14(+) DCs primed CD4(+) T cells into cells that induce naive B cells to switch isotype and become plasma cells. In contrast, LCs preferentially induced the differentiation of CD4(+) T cells secreting T helper 2 (Th2) cell cytokines and were efficient at priming and cross-priming naive CD8(+) T cells. A third DC population, CD14(-)CD207(-)CD1a(+) DC, which resides in the dermis, could activate CD8(+) T cells better than CD14(+) DCs but less efficiently than LCs. Thus, the human skin displays three DC subsets, two of which, i.e., CD14(+) DCs and LCs, display functional specializations, the preferential activation of humoral and cellular immunity, respectively.
引用
收藏
页码:497 / 510
页数:14
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