These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
112 related articles for article (PubMed ID: 17240458)
1. An interferon-gamma-producing Th1 subset is the major source of IL-17 in experimental autoimmune encephalitis. Suryani S; Sutton I J Neuroimmunol; 2007 Feb; 183(1-2):96-103. PubMed ID: 17240458 [TBL] [Abstract][Full Text] [Related]
2. Infiltration of Th1 and Th17 cells and activation of microglia in the CNS during the course of experimental autoimmune encephalomyelitis. Murphy AC; Lalor SJ; Lynch MA; Mills KH Brain Behav Immun; 2010 May; 24(4):641-51. PubMed ID: 20138983 [TBL] [Abstract][Full Text] [Related]
3. The central nervous system environment controls effector CD4+ T cell cytokine profile in experimental allergic encephalomyelitis. Krakowski ML; Owens T Eur J Immunol; 1997 Nov; 27(11):2840-7. PubMed ID: 9394808 [TBL] [Abstract][Full Text] [Related]
4. Invariant NKT cells producing IL-4 or IL-10, but not IFN-gamma, inhibit the Th1 response in experimental autoimmune encephalomyelitis, whereas none of these cells inhibits the Th17 response. Oh SJ; Chung DH J Immunol; 2011 Jun; 186(12):6815-21. PubMed ID: 21572032 [TBL] [Abstract][Full Text] [Related]
5. CD4+ICOS+ T lymphocytes inhibit T cell activation 'in vitro' and attenuate autoimmune encephalitis 'in vivo'. Rojo JM; Pini E; Ojeda G; Bello R; Dong C; Flavell RA; Dianzani U; Portolés P Int Immunol; 2008 Apr; 20(4):577-89. PubMed ID: 18310064 [TBL] [Abstract][Full Text] [Related]
6. Interferon-γ orchestrates the number and function of Th17 cells in experimental autoimmune encephalomyelitis. Berghmans N; Nuyts A; Uyttenhove C; Van Snick J; Opdenakker G; Heremans H J Interferon Cytokine Res; 2011 Jul; 31(7):575-87. PubMed ID: 21348780 [TBL] [Abstract][Full Text] [Related]
7. IL-12/IFN-gamma/NO axis plays critical role in development of Th1-mediated experimental autoimmune encephalomyelitis. Xiao BG; Ma CG; Xu LY; Link H; Lu CZ Mol Immunol; 2008 Feb; 45(4):1191-6. PubMed ID: 17697713 [TBL] [Abstract][Full Text] [Related]
8. Activation of invariant NKT cells by alphaGalCer administration protects mice from MOG35-55-induced EAE: critical roles for administration route and IFN-gamma. Furlan R; Bergami A; Cantarella D; Brambilla E; Taniguchi M; Dellabona P; Casorati G; Martino G Eur J Immunol; 2003 Jul; 33(7):1830-8. PubMed ID: 12811843 [TBL] [Abstract][Full Text] [Related]
9. Upregulation of interferon-gamma and interleukin-4, Th cell-derived cytokines by So-Shi-Ho-Tang (Sho-Saiko-To) occurs at the level of antigen presenting cells, but not CD4 T cells. Kang H; Choi TW; Ahn KS; Lee JY; Ham IH; Choi HY; Shim ES; Sohn NW J Ethnopharmacol; 2009 May; 123(1):6-14. PubMed ID: 19429332 [TBL] [Abstract][Full Text] [Related]
11. Crucial role of the interleukin-6/interleukin-17 cytokine axis in the induction of arthritis by glucose-6-phosphate isomerase. Iwanami K; Matsumoto I; Tanaka-Watanabe Y; Inoue A; Mihara M; Ohsugi Y; Mamura M; Goto D; Ito S; Tsutsumi A; Kishimoto T; Sumida T Arthritis Rheum; 2008 Mar; 58(3):754-63. PubMed ID: 18311788 [TBL] [Abstract][Full Text] [Related]
12. Critical role of preproenkephalin in experimental autoimmune encephalomyelitis. Weir C; McNeill A; Hook S; Harvie M; La Flamme AC; Le Gros G; Bäckström BT J Neuroimmunol; 2006 Oct; 179(1-2):18-25. PubMed ID: 16904193 [TBL] [Abstract][Full Text] [Related]
13. A chimeric TCR-beta chain confers increased susceptibility to EAE. Petersen TR; Lata R; Spittle E; Bäckström BT Mol Immunol; 2007 Jul; 44(14):3473-81. PubMed ID: 17481734 [TBL] [Abstract][Full Text] [Related]
14. CD62L is required for the priming of encephalitogenic T cells but does not play a major role in the effector phase of experimental autoimmune encephalomyelitis. Li O; Liu JQ; Zhang H; Zheng P; Liu Y; Bai XF Scand J Immunol; 2006 Aug; 64(2):117-24. PubMed ID: 16867156 [TBL] [Abstract][Full Text] [Related]
15. Pathophysiology of interleukin-23 in experimental autoimmune encephalomyelitis. Touil T; Fitzgerald D; Zhang GX; Rostami AM; Gran B Drug News Perspect; 2006 Mar; 19(2):77-83. PubMed ID: 16628262 [TBL] [Abstract][Full Text] [Related]
16. Host T cells are the main producers of IL-17 within the central nervous system during initiation of experimental autoimmune encephalomyelitis induced by adoptive transfer of Th1 cell lines. Lees JR; Iwakura Y; Russell JH J Immunol; 2008 Jun; 180(12):8066-72. PubMed ID: 18523270 [TBL] [Abstract][Full Text] [Related]
17. Inflammation in the central nervous system and Th17 responses are inhibited by IFN-gamma-Induced IL-18 binding protein. Millward JM; Løbner M; Wheeler RD; Owens T J Immunol; 2010 Aug; 185(4):2458-66. PubMed ID: 20644165 [TBL] [Abstract][Full Text] [Related]
18. Differential roles for IFN-gamma and IL-17 in experimental autoimmune uveoretinitis. Yoshimura T; Sonoda KH; Miyazaki Y; Iwakura Y; Ishibashi T; Yoshimura A; Yoshida H Int Immunol; 2008 Feb; 20(2):209-14. PubMed ID: 18156624 [TBL] [Abstract][Full Text] [Related]
19. Astrocytes stimulate interleukin-17 and interferon-gamma production in vitro. Miljkovic D; Momcilovic M; Stojanovic I; Stosic-Grujicic S; Ramic Z; Mostarica-Stojkovic M J Neurosci Res; 2007 Dec; 85(16):3598-606. PubMed ID: 17969033 [TBL] [Abstract][Full Text] [Related]
20. IL-23-driven encephalo-tropism and Th17 polarization during CNS-inflammation in vivo. Gyülvészi G; Haak S; Becher B Eur J Immunol; 2009 Jul; 39(7):1864-9. PubMed ID: 19544494 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]