TY - JOUR
T1 - Plasmacytoid Dendritic Cells Transport Peripheral Antigens to the Thymus to Promote Central Tolerance
AU - Hadeiba, Husein
AU - Lahl, Katharina
AU - Edalati, Abdolhossein
AU - Oderup, Cecilia
AU - Habtezion, Aida
AU - Pachynski, Russell
AU - Nguyen, Linh
AU - Ghodsi, Asma
AU - Adler, Sarah
AU - Butcher, Eugene C.
N1 - Funding Information:
We thank L. Rott for assistance and G. Dranoff for the Flt3L-expressing B16 melanoma line. H.H. is a recipient of an Investigator Career Award from the Arthritis Foundation and was a fellow under the NIH Training Grant AI07290; K.L. is a fellow of the Deutsche Forschungsgemeinschaft, DFG; C.O. was supported by Fellowships from the Wenner-Gren Foundation and the Crohn's & Colitis Foundation; and A.H. was supported by NIH grant DK085426. The work was supported by NIH grants R01AI093981, AI047822, and DK084647 to E.C.B., the Stanford Digestive Disease Center under DK056339, and a Merit Award from the Department of Veterans Affairs.
PY - 2012/3/23
Y1 - 2012/3/23
N2 - Central tolerance can be mediated by peripheral dendritic cells (DCs) that transport innocuous antigens (Ags) to the thymus for presentation to developing T cells, but the responsible DC subsets remained poorly defined. Immature plasmacytoid DCs (pDCs) express CCR9, a chemokine receptor involved in migration of T cell precursors to the thymus. We show here that CCR9 mediated efficient thymic entry of endogenous or i.v. transfused pDCs. pDCs activated by Toll-like receptor (TLR) ligands downregulated CCR9 and lost their ability to home to the thymus. Moreover, endogenous pDCs took up subcutaneously injected fluorescent Ag and, in the absence of TLR signals, transported Ag to the thymus in a CCR9-dependent fashion. Injected, Ag-loaded pDCs effectively deleted Ag-specific thymocytes, and this thymic clonal deletion required CCR9-mediated homing and was prevented by infectious signals. Thus, peripheral pDCs can contribute to immune tolerance through CCR9-dependent transport of peripheral Ags and subsequent deletion of Ag-reactive thymocytes.
AB - Central tolerance can be mediated by peripheral dendritic cells (DCs) that transport innocuous antigens (Ags) to the thymus for presentation to developing T cells, but the responsible DC subsets remained poorly defined. Immature plasmacytoid DCs (pDCs) express CCR9, a chemokine receptor involved in migration of T cell precursors to the thymus. We show here that CCR9 mediated efficient thymic entry of endogenous or i.v. transfused pDCs. pDCs activated by Toll-like receptor (TLR) ligands downregulated CCR9 and lost their ability to home to the thymus. Moreover, endogenous pDCs took up subcutaneously injected fluorescent Ag and, in the absence of TLR signals, transported Ag to the thymus in a CCR9-dependent fashion. Injected, Ag-loaded pDCs effectively deleted Ag-specific thymocytes, and this thymic clonal deletion required CCR9-mediated homing and was prevented by infectious signals. Thus, peripheral pDCs can contribute to immune tolerance through CCR9-dependent transport of peripheral Ags and subsequent deletion of Ag-reactive thymocytes.
UR - http://www.scopus.com/inward/record.url?scp=84858786391&partnerID=8YFLogxK
U2 - 10.1016/j.immuni.2012.01.017
DO - 10.1016/j.immuni.2012.01.017
M3 - Article
C2 - 22444632
AN - SCOPUS:84858786391
SN - 1074-7613
VL - 36
SP - 438
EP - 450
JO - Immunity
JF - Immunity
IS - 3
ER -