TY - JOUR
T1 - Functional Specializations of Human Epidermal Langerhans Cells and CD14+ Dermal Dendritic Cells
AU - Klechevsky, Eynav
AU - Morita, Rimpei
AU - Liu, Maochang
AU - Cao, Yanying
AU - Coquery, Sebastien
AU - Thompson-Snipes, Lu Ann
AU - Briere, Francine
AU - Chaussabel, Damien
AU - Zurawski, Gerard
AU - Palucka, A. Karolina
AU - Reiter, Yoram
AU - Banchereau, Jacques
AU - Ueno, Hideki
N1 - Funding Information:
We thank E. Kowalski, J. Shay, Q. Nguyen, C. Glaser, and S.S. Clayton for their help. We thank J. Duncan and surgeons and nurses from the Plastic Surgery Department for skin samples. We thank R. Germain, I. Mellman, and C. Harrod for critical reading and discussion and M. Ramsay, W. Duncan, and C. Samuelsen for continuous support. This work was supported by grants from Baylor Health Care System Foundation and the National Institutes of Health (RO-1 CA78846, RO-1 CA85540, PO-1 CA84512, and U-19 AI-57234 to J.B.) and a scholarship from Uehara Memorial Foundation (to H.U.). J.B. holds the W.W. Caruth, Jr. Chair for Transplantation Immunology Research. A.K.P. holds the Ramsay Chair for Cancer Immunology. J.B. holds stock options in Argos Therapeutics, a private company that is testing the potential therapeutic applications of dendritic cells.
PY - 2008/9/19
Y1 - 2008/9/19
N2 - 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.
AB - 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.
KW - CELLIMMUNO
UR - http://www.scopus.com/inward/record.url?scp=51349093240&partnerID=8YFLogxK
U2 - 10.1016/j.immuni.2008.07.013
DO - 10.1016/j.immuni.2008.07.013
M3 - Article
C2 - 18789730
AN - SCOPUS:51349093240
SN - 1074-7613
VL - 29
SP - 497
EP - 510
JO - Immunity
JF - Immunity
IS - 3
ER -