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Functional specializations of human epidermal langerhans cells and CD14+ dermal dendritic cells
被引:480
|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
来源:
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.
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页码:497 / 510
页数:14
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