TY - JOUR
T1 - GM-CSF-licensed CD11b+ lung dendritic cells orchestrate Th2 immunity to Blomia tropicalis
AU - Zhou, Qian
AU - Ho, Adrian W.S.
AU - Schlitzer, Andreas
AU - Tang, Yafang
AU - Wong, Kenneth H.S.
AU - Wong, Fiona H.S.
AU - Chua, Yen Leong
AU - Angeli, Veronique
AU - Mortellaro, Alessandra
AU - Ginhoux, Florent
AU - Kemeny, David M.
PY - 2014/7/15
Y1 - 2014/7/15
N2 - The Blomia tropicalis dust mite is prevalent in tropical and subtropical regions of the world. Although it is a leading cause of asthma, little is known how it induces allergy. Using a novel murine asthma model induced by intranasal exposure to B. tropicalis, we observed that a single intranasal sensitization to B. tropicalis extract induces strong Th2 priming in the lung draining lymph node. Resident CD11b+ dendritic cells (DCs) preferentially transport Ag from the lung to the draining lymph node and are crucial for the initiation of Th2 CD4+ T cell responses. As a consequence, mice selectively deficient in CD11b+ DCs exhibited attenuated Th2 responses and more importantly did not develop any allergic inflammation. Conversely, mice deficient in CD103+ DCs and CCR2-dependent monocyte-derived DCs exhibited similar allergic inflammation compared with their wild-type counterparts. We also show that CD11b+ DCs constitutively express higher levels of GM-CSF receptor compared with CD103+ DCs and are thus selectively licensed by lung epithelial-derived GM-CSF to induce Th2 immunity. Taken together, our study identifies GM-CSF- licensed CD11b + lung DCs as a key component for induction of Th2 responses and represents a potential target for therapeutic intervention in allergy.
AB - The Blomia tropicalis dust mite is prevalent in tropical and subtropical regions of the world. Although it is a leading cause of asthma, little is known how it induces allergy. Using a novel murine asthma model induced by intranasal exposure to B. tropicalis, we observed that a single intranasal sensitization to B. tropicalis extract induces strong Th2 priming in the lung draining lymph node. Resident CD11b+ dendritic cells (DCs) preferentially transport Ag from the lung to the draining lymph node and are crucial for the initiation of Th2 CD4+ T cell responses. As a consequence, mice selectively deficient in CD11b+ DCs exhibited attenuated Th2 responses and more importantly did not develop any allergic inflammation. Conversely, mice deficient in CD103+ DCs and CCR2-dependent monocyte-derived DCs exhibited similar allergic inflammation compared with their wild-type counterparts. We also show that CD11b+ DCs constitutively express higher levels of GM-CSF receptor compared with CD103+ DCs and are thus selectively licensed by lung epithelial-derived GM-CSF to induce Th2 immunity. Taken together, our study identifies GM-CSF- licensed CD11b + lung DCs as a key component for induction of Th2 responses and represents a potential target for therapeutic intervention in allergy.
UR - http://www.scopus.com/inward/record.url?scp=84904258454&partnerID=8YFLogxK
U2 - 10.4049/jimmunol.1303138
DO - 10.4049/jimmunol.1303138
M3 - Article
C2 - 24943219
AN - SCOPUS:84904258454
SN - 0022-1767
VL - 193
SP - 496
EP - 509
JO - Journal of Immunology
JF - Journal of Immunology
IS - 2
ER -