| Literature DB >> 18789730 |
Eynav Klechevsky1, Rimpei Morita, Maochang Liu, Yanying Cao, Sebastien Coquery, Luann Thompson-Snipes, Francine Briere, Damien Chaussabel, Gerard Zurawski, A Karolina Palucka, Yoram Reiter, Jacques Banchereau, Hideki Ueno.
Abstract
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 crosspriming 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.Entities:
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Year: 2008 PMID: 18789730 PMCID: PMC2688399 DOI: 10.1016/j.immuni.2008.07.013
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745