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Journal Abstract Search


860 related items for PubMed ID: 8912892

  • 21. Synovial fibroblasts as accessory cells for staphylococcal enterotoxin-mediated T-cell activation.
    Kraft M, Filsinger S, Krämer KL, Kabelitz D, Hänsch GM, Schoels M.
    Immunology; 1995 Jul; 85(3):461-6. PubMed ID: 7558136
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  • 22. Expansion and clonal deletion of peripheral T cells induced by bacterial superantigen is independent of the interleukin-2 pathway.
    Gonzalo JA, Moreno de Alborán I, Alés-Martínez JE, Martínez C, Kroemer G.
    Eur J Immunol; 1992 Apr; 22(4):1007-11. PubMed ID: 1551401
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  • 23. Human leukocyte antigen-class II-negative long-term cultured human T-cell leukemia virus type-I-infected T-cell lines with progressed cytological properties significantly induce superantigen-dependent normal T-cell proliferation.
    Nagasaki M, Zhang J, Morikawa S, Harada T, Nabika T, Tanaka Y.
    Pathol Int; 2005 May; 55(5):264-72. PubMed ID: 15871724
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  • 24. Superantigen-induced anergy in cytotoxic CD8+ T cells.
    Sundstedt A, Höidén I, Hansson J, Hedlund G, Kalland T, Dohlsten M.
    J Immunol; 1995 Jun 15; 154(12):6306-13. PubMed ID: 7759869
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  • 25. Macrophages are dispensable for superantigen-mediated stimulation and anergy induction of peripheral T cells in vivo.
    Koesling M, Rott O, Fleischer B.
    Cell Immunol; 1994 Aug 15; 157(1):29-37. PubMed ID: 8039249
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  • 28. Skin homing (cutaneous lymphocyte-associated antigen-positive) CD8+ T cells respond to superantigen and contribute to eosinophilia and IgE production in atopic dermatitis.
    Akdis M, Simon HU, Weigl L, Kreyden O, Blaser K, Akdis CA.
    J Immunol; 1999 Jul 01; 163(1):466-75. PubMed ID: 10384150
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  • 31. In vivo responses of CD4+ and CD8+ cells to bacterial superantigens.
    Herrmann T, Baschieri S, Lees RK, MacDonald HR.
    Eur J Immunol; 1992 Jul 01; 22(7):1935-8. PubMed ID: 1623932
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  • 32. In vivo staphylococcal enterotoxin B (SEB)-primed murine splenocytes secrete mediators which suppress CD25(hi) expression and cell cycle progression of naive splenocytes in response to SEB in vitro.
    Hsu LJ, Jan MS, Lin YS.
    Cell Immunol; 2000 Apr 10; 201(1):50-7. PubMed ID: 10805973
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  • 34. Staphylococcal enterotoxin B induces the expression of activation markers on murine memory T cells in the absence of proliferation or lymphokine secretion.
    Lee WT, Thrush GR, Vitetta ES.
    Cell Immunol; 1995 Apr 15; 162(1):26-32. PubMed ID: 7704907
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  • 37. Differential in vivo effects of a superantigen and an antibody targeted to the same T cell receptor. Activation-induced cell death vs passive macrophage-dependent deletion.
    Gonzalo JA, Baixeras E, González-García A, George-Chandy A, Van Rooijen N, Martínez C, Kroemer G.
    J Immunol; 1994 Feb 15; 152(4):1597-608. PubMed ID: 8120373
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  • 38. TNF-alpha, not CD154 (CD40L), plays a major role in SEB-dependent, CD4(+) T cell-induced endothelial cell activation in vitro.
    Baum D, Yaron R, Yellin MJ.
    Cell Immunol; 1998 Nov 25; 190(1):12-22. PubMed ID: 9826442
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  • 39. Synergistic effect between CD40 and class II signals overcome the requirement for class II dimerization in superantigen-induced cytokine gene expression.
    Mehindate K, al-Daccak R, Damdoumi F, Mourad W.
    Eur J Immunol; 1996 Sep 25; 26(9):2075-80. PubMed ID: 8814249
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  • 40. Activation of murine T cells by toxic shock syndrome toxin-1. The toxin-binding structures expressed on murine accessory cells are MHC class II molecules.
    Uchiyama T, Tadakuma T, Imanishi K, Araake M, Saito S, Yan XJ, Fujikawa H, Igarashi H, Yamaura N.
    J Immunol; 1989 Nov 15; 143(10):3175-82. PubMed ID: 2509554
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