Activation of invariant NKT cells by αGalCer administration protects mice from MOG35–55-induced EAE: critical roles for administration route and IFN-γ

2003 ◽  
Vol 33 (7) ◽  
pp. 1830-1838 ◽  
Author(s):  
Roberto Furlan ◽  
Alessandra Bergami ◽  
Daniela Cantarella ◽  
Elena Brambilla ◽  
Masaro Taniguchi ◽  
...  
2008 ◽  
Vol 181 (7) ◽  
pp. 4791-4797 ◽  
Author(s):  
Rafael S. Grajewski ◽  
Anna M. Hansen ◽  
Rajeev K. Agarwal ◽  
Mitchell Kronenberg ◽  
Stephane Sidobre ◽  
...  
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2008 ◽  
Vol 181 (4) ◽  
pp. 2446-2454 ◽  
Author(s):  
María Moreno ◽  
Johan W. Molling ◽  
Silvia von Mensdorff-Pouilly ◽  
René H. M. Verheijen ◽  
Erik Hooijberg ◽  
...  

2009 ◽  
Vol 184 (3) ◽  
pp. 1242-1250 ◽  
Author(s):  
Stephen R. Mattarollo ◽  
Azad Rahimpour ◽  
Allison Choyce ◽  
Dale I. Godfrey ◽  
Graham R. Leggatt ◽  
...  
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2012 ◽  
Vol 188 (3) ◽  
pp. 931.1-931
Author(s):  
Ting Hu ◽  
Hongmei Zhu ◽  
He Wang ◽  
Shanling Liu
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2010 ◽  
Vol 186 (1) ◽  
pp. 284-290 ◽  
Author(s):  
Françoise Grela ◽  
Aude Aumeunier ◽  
Emilie Bardel ◽  
Linh Pham Van ◽  
Elvire Bourgeois ◽  
...  

2005 ◽  
Vol 73 (11) ◽  
pp. 7541-7547 ◽  
Author(s):  
Mattias Svensson ◽  
Soombul Zubairi ◽  
Asher Maroof ◽  
Fatima Kazi ◽  
Masaru Taniguchi ◽  
...  

ABSTRACT Gamma interferon (IFN-γ)-regulated chemokines of the CXC family have been implicated as key regulators of a variety of T-cell-dependent inflammatory processes. However, the cellular source(s) of IFN-γ that regulates their early expression has rarely been defined. Here, we have directly addressed this question in mice after Leishmania donovani infection. Comparison of CXCL10 mRNA accumulation in normal and IFN-γ-deficient mice confirmed an absolute requirement for IFN-γ for sustained (24 h) expression of CXCL10 mRNA accumulation in this model. In normal mice, IFN-γ was produced by both CD3int NK1.1+ NKT cells and CD3− NK1.1+ NK cells, as detected by intracellular flow cytometry. Strikingly, B6.Jα281−/− mice lacking NKT cells that express the invariant Vα14Jα18 T-cell-receptor α chain, although retaining a significant population of IFN-γ-producing NK cells and NKT cells, were unable to sustain CXCL10 mRNA accumulation. These data indicate that invariant NKT cells are indispensable for the regulation of hepatic CXCL10 gene expression during L. donovani infection.


2017 ◽  
Vol 103 (1) ◽  
pp. 99-106 ◽  
Author(s):  
Dongjin Jeong ◽  
Hye Young Kim ◽  
Doo Hyun Chung

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