281 related articles for article (PubMed ID: 15100264)
21. Accessory protein-like is essential for IL-18-mediated signaling.
Cheung H; Chen NJ; Cao Z; Ono N; Ohashi PS; Yeh WC
J Immunol; 2005 May; 174(9):5351-7. PubMed ID: 15843532
[TBL] [Abstract][Full Text] [Related]
22. IL-4-producing NK T cells are biased towards IFN-gamma production by IL-12. Influence of the microenvironment on the functional capacities of NK T cells.
Leite-De-Moraes MC; Moreau G; Arnould A; Machavoine F; Garcia C; Papiernik M; Dy M
Eur J Immunol; 1998 May; 28(5):1507-15. PubMed ID: 9603455
[TBL] [Abstract][Full Text] [Related]
23. IL-1 receptor-associated kinase 4 is essential for IL-18-mediated NK and Th1 cell responses.
Suzuki N; Chen NJ; Millar DG; Suzuki S; Horacek T; Hara H; Bouchard D; Nakanishi K; Penninger JM; Ohashi PS; Yeh WC
J Immunol; 2003 Apr; 170(8):4031-5. PubMed ID: 12682231
[TBL] [Abstract][Full Text] [Related]
24. Indispensable role for TNF-alpha and IFN-gamma at the effector phase of liver injury mediated by Th1 cells specific to hepatitis B virus surface antigen.
Ohta A; Sekimoto M; Sato M; Koda T; Nishimura S; Iwakura Y; Sekikawa K; Nishimura T
J Immunol; 2000 Jul; 165(2):956-61. PubMed ID: 10878371
[TBL] [Abstract][Full Text] [Related]
25. IFN-gamma receptor signaling is essential for the initiation, acceleration, and destruction of autoimmune kidney disease in MRL-Fas(lpr) mice.
Schwarting A; Wada T; Kinoshita K; Tesch G; Kelley VR
J Immunol; 1998 Jul; 161(1):494-503. PubMed ID: 9647261
[TBL] [Abstract][Full Text] [Related]
26. IL-12 administration accelerates autoimmune diabetes in both wild-type and IFN-gamma-deficient nonobese diabetic mice, revealing pathogenic and protective effects of IL-12-induced IFN-gamma.
Trembleau S; Penna G; Gregori S; Giarratana N; Adorini L
J Immunol; 2003 Jun; 170(11):5491-501. PubMed ID: 12759426
[TBL] [Abstract][Full Text] [Related]
27. Dendritic cells are resistant to apoptosis through the Fas (CD95/APO-1) pathway.
Ashany D; Savir A; Bhardwaj N; Elkon KB
J Immunol; 1999 Nov; 163(10):5303-11. PubMed ID: 10553053
[TBL] [Abstract][Full Text] [Related]
28. Gammadelta T cells promote a Th1 response during coxsackievirus B3 infection in vivo: role of Fas and Fas ligand.
Huber S; Shi C; Budd RC
J Virol; 2002 Jul; 76(13):6487-94. PubMed ID: 12050361
[TBL] [Abstract][Full Text] [Related]
29. IL-12 deficiency in MRL-Fas(lpr) mice delays nephritis and intrarenal IFN-gamma expression, and diminishes systemic pathology.
Kikawada E; Lenda DM; Kelley VR
J Immunol; 2003 Apr; 170(7):3915-25. PubMed ID: 12646661
[TBL] [Abstract][Full Text] [Related]
30. Simultaneous exposure to interleukin-18 and interleukin-10 in vitro synergistically augments murine spleen natural killer cell activity.
Micallef MJ; Tanimoto T; Torigoe K; Nishida Y; Kohno K; Ikegami H; Kurimoto M
Cancer Immunol Immunother; 1999; 48(2-3):109-17. PubMed ID: 10414464
[TBL] [Abstract][Full Text] [Related]
31. IL-4-producing NK1.1+ T cells are resistant to glucocorticoid-induced apoptosis: implications for the Th1/Th2 balance.
Tamada K; Harada M; Abe K; Li T; Nomoto K
J Immunol; 1998 Aug; 161(3):1239-47. PubMed ID: 9686584
[TBL] [Abstract][Full Text] [Related]
32. Development of intestinal intraepithelial lymphocytes, NK cells, and NK 1.1+ T cells in CD45-deficient mice.
Martin SM; Mehta IK; Yokoyama WM; Thomas ML; Lorenz RG
J Immunol; 2001 May; 166(10):6066-73. PubMed ID: 11342624
[TBL] [Abstract][Full Text] [Related]
33. Recruitment of hepatic NK cells by IL-12 is dependent on IFN-gamma and VCAM-1 and is rapidly down-regulated by a mechanism involving T cells and expression of Fas.
Fogler WE; Volker K; Watanabe M; Wigginton JM; Roessler P; Brunda MJ; Ortaldo JR; Wiltrout RH
J Immunol; 1998 Dec; 161(11):6014-21. PubMed ID: 9834083
[TBL] [Abstract][Full Text] [Related]
34. Type 1 cytokine/chemokine production by mouse NK cells following activation of their TLR/MyD88-mediated pathways.
Sawaki J; Tsutsui H; Hayashi N; Yasuda K; Akira S; Tanizawa T; Nakanishi K
Int Immunol; 2007 Mar; 19(3):311-20. PubMed ID: 17289654
[TBL] [Abstract][Full Text] [Related]
35. NK T cell precursors exhibit differential cytokine regulation and require Itk for efficient maturation.
Gadue P; Stein PL
J Immunol; 2002 Sep; 169(5):2397-406. PubMed ID: 12193707
[TBL] [Abstract][Full Text] [Related]
36. Synergistic proliferation and activation of natural killer cells by interleukin 12 and interleukin 18.
Lauwerys BR; Renauld JC; Houssiau FA
Cytokine; 1999 Nov; 11(11):822-30. PubMed ID: 10547269
[TBL] [Abstract][Full Text] [Related]
37. Inflammasome and Fas-Mediated IL-1β Contributes to Th17/Th1 Cell Induction in Pathogenic Bacterial Infection In Vivo.
Uchiyama R; Yonehara S; Taniguchi S; Ishido S; Ishii KJ; Tsutsui H
J Immunol; 2017 Aug; 199(3):1122-1130. PubMed ID: 28674179
[TBL] [Abstract][Full Text] [Related]
38. Peripheral immature CD2-/low T cell development from type 2 to type 1 cytokine production.
Loza MJ; Perussia B
J Immunol; 2002 Sep; 169(6):3061-8. PubMed ID: 12218122
[TBL] [Abstract][Full Text] [Related]
39. Enhancement of the synthetic ligand-mediated function of liver NK1.1Ag+ T cells in mice by interleukin-12 pretreatment.
Habu Y; Uchida T; Inui T; Nakashima H; Fukasawa M; Seki S
Immunology; 2004 Sep; 113(1):35-43. PubMed ID: 15312134
[TBL] [Abstract][Full Text] [Related]
40. Fas involvement in human NK cell apoptosis: lack of a requirement for CD16-mediated events.
Ortaldo JR; Winkler-Pickett RT; Nagata S; Ware CF
J Leukoc Biol; 1997 Feb; 61(2):209-15. PubMed ID: 9021927
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]