Blocking Antigen Transport To Resident Lymph Node Dendritic Cells Prevents CD4+ T-cell Priming

2011 ◽  
Vol 127 (2) ◽  
pp. AB93-AB93
Author(s):  
J.A. Steinberg ◽  
A. Mahajan ◽  
H.M.A. Simkins ◽  
T.M. Laufer
2015 ◽  
Vol 11 (10) ◽  
pp. e1005206 ◽  
Author(s):  
Vishnu Priya Bollampalli ◽  
Lívia Harumi Yamashiro ◽  
Xiaogang Feng ◽  
Damiën Bierschenk ◽  
Yu Gao ◽  
...  

2010 ◽  
Vol 184 (6) ◽  
pp. 2873-2885 ◽  
Author(s):  
Jennifer J. Linderman ◽  
Thomas Riggs ◽  
Manjusha Pande ◽  
Mark Miller ◽  
Simeone Marino ◽  
...  
Keyword(s):  
T Cell ◽  

2008 ◽  
Vol 181 (6) ◽  
pp. 3965-3973 ◽  
Author(s):  
Annette Busch ◽  
Thomas Quast ◽  
Sascha Keller ◽  
Waldemar Kolanus ◽  
Percy Knolle ◽  
...  

Immunology ◽  
2013 ◽  
Vol 139 (2) ◽  
pp. 219-226 ◽  
Author(s):  
Seema Shrivastava ◽  
Liang Ma ◽  
El-Li Tham ◽  
John H. McVey ◽  
Daxin Chen ◽  
...  

2014 ◽  
Vol 211 (6) ◽  
pp. 1153-1166 ◽  
Author(s):  
Juan Dubrot ◽  
Fernanda V. Duraes ◽  
Lambert Potin ◽  
Francesca Capotosti ◽  
Dale Brighouse ◽  
...  

Dendritic cells (DCs), and more recently lymph node stromal cells (LNSCs), have been described to tolerize self-reactive CD8+ T cells in LNs. Although LNSCs express MHCII, it is unknown whether they can also impact CD4+ T cell functions. We show that the promoter IV (pIV) of class II transactivator (CIITA), the master regulator of MHCII expression, controls endogenous MHCII expression by LNSCs. Unexpectedly, LNSCs also acquire peptide–MHCII complexes from DCs and induce CD4+ T cell dysfunction by presenting transferred complexes to naive CD4+ T cells and preventing their proliferation and survival. Our data reveals a novel, alternative mechanism where LN-resident stromal cells tolerize CD4+ T cells through the presentation of self-antigens via transferred peptide–MHCII complexes of DC origin.


Author(s):  
Francesca Aloisi ◽  
Francesco Ria ◽  
Sandra Columba-Cabezas ◽  
Henry Hess ◽  
Giuseppe Penna ◽  
...  

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