TY - JOUR
T1 - Epithelial control of the human pDC response to extracellular bacteria
AU - Michea, Paula
AU - Vargas, Pablo
AU - Donnadieu, Marie Hélène
AU - Rosemblatt, Mario
AU - Bono, María Rosa
AU - Duménil, Guillaume
AU - Soumelis, Vassili
PY - 2013/4
Y1 - 2013/4
N2 - Plasmacytoid pre-dendritic cells (pDCs) are specialized in responding to nucleic acids, and link innate with adaptive immunity. Although the response of pDCs to viruses is well established, whether pDCs can respond to extracellular bacteria remains controversial. Here, we demonstrate that extracellular bacteria such as Neisseria meningitidis, Haemophilus influenzae, and Staphylococcus aureus activate pDCs to produce IFN-α, TNF-α, IL-6, and to upregulate CD86 expression. We observed that pDCs were present within tonsillar crypts and oro-nasopharyngeal epithelium, where they may contact extracellular bacteria, in situ. Tonsil epithelium-conditioned supernatants inhibited IFN-α, TNF-α, and IL-6 triggered by the direct contact of N. meningitidis or S. aureus with pDCs. However, pDC priming of naive T cells was not affected, suggesting that tonsil epithelium micro-environment limits local inflammation while preserving adaptive immunity in response to extracellular bacteria. Our results reveal an important and novel function of pDCs in the initiation of the mucosal innate and adaptive immunity to extracellular bacteria.
AB - Plasmacytoid pre-dendritic cells (pDCs) are specialized in responding to nucleic acids, and link innate with adaptive immunity. Although the response of pDCs to viruses is well established, whether pDCs can respond to extracellular bacteria remains controversial. Here, we demonstrate that extracellular bacteria such as Neisseria meningitidis, Haemophilus influenzae, and Staphylococcus aureus activate pDCs to produce IFN-α, TNF-α, IL-6, and to upregulate CD86 expression. We observed that pDCs were present within tonsillar crypts and oro-nasopharyngeal epithelium, where they may contact extracellular bacteria, in situ. Tonsil epithelium-conditioned supernatants inhibited IFN-α, TNF-α, and IL-6 triggered by the direct contact of N. meningitidis or S. aureus with pDCs. However, pDC priming of naive T cells was not affected, suggesting that tonsil epithelium micro-environment limits local inflammation while preserving adaptive immunity in response to extracellular bacteria. Our results reveal an important and novel function of pDCs in the initiation of the mucosal innate and adaptive immunity to extracellular bacteria.
KW - Cytokines
KW - Extracellular bacteria
KW - Human mucosa
KW - Innate immunity
KW - Plasmacytoid pre-dendritic cell
UR - http://www.scopus.com/inward/record.url?scp=84876856425&partnerID=8YFLogxK
U2 - 10.1002/eji.201242990
DO - 10.1002/eji.201242990
M3 - Article
C2 - 23436642
AN - SCOPUS:84876856425
SN - 0014-2980
VL - 43
SP - 1264
EP - 1273
JO - European Journal of Immunology
JF - European Journal of Immunology
IS - 5
ER -