TMP778, a selective inhibitor of RORγt, suppresses experimental autoimmune uveitis development, but affects both Th17 and Th1 cell populations
Author:
Affiliation:
1. Laboratory of Immunology; National Eye Institute; National Institutes of Health; Bethesda MD USA
2. State Key Laboratory of Ophthalmology; Zhongshan Ophthalmic Center; Sun Yat-Sen University; Guangzhou China
3. GlaxoSmithKline; Cambridge MA USA
Funder
Intramural Program of the National Eye Institute (NEI)
National Institutes of Health
Publisher
Wiley
Subject
Immunology,Immunology and Allergy
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/eji.201747029/fullpdf
Reference27 articles.
1. Differentiation of effector CD4 T cell populations (*);Zhu;Annu. Rev. Immunol.,2010
2. Role of Th1 and Th17 cells in organ-specific autoimmunity;Dardalhon;J. Autoimmun.,2008
3. IL-17 and Th17 cells;Korn;Annu. Rev. Immunol.,2009
4. Either a Th17 or a Th1 effector response can drive autoimmunity: conditions of disease induction affect dominant effector category;Luger;J. Exp. Med.,2008
5. Th17 cells in inflammation and autoimmunity;Singh;Autoimmun. Rev.,2014
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