Epithelial control of the human pDC response to extracellular bacteria
Author
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Michea, Paula
Author
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Vargas, Pablo
es_CL
Author
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Donnadieu, Marie-Hélène
es_CL
Author
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Rosemblatt Silber, Mario César
es_CL
Author
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Bono Merino, María Rosa
es_CL
Author
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Duménil, Guillaume
es_CL
Author
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Soumelis, Vassili
es_CL
Admission date
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2014-01-28T18:59:56Z
Available date
dc.date.available
2014-01-28T18:59:56Z
Publication date
dc.date.issued
2013
Cita de ítem
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Eur. J. Immunol. 2013. 43: 1264–1273
en_US
Identifier
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DOI: 10.1002/eji.201242990
Identifier
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https://repositorio.uchile.cl/handle/2250/119725
General note
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Artículo de publicación ISI
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Abstract
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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 microenvironment
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.
en_US
Patrocinador
dc.description.sponsorship
This work was supported by grants from International
Cooperation Inserm-Conicyt 2009/2011, Conicyt Doctoral Fellowship,
Conicyt PFB-16, Universit´e Paris-5 Ren´e Descartes Mobility
fellowship, Agence Nationale de la Recherche (ANR), and Fondation
pour le Recherche M´edicale (FRM).