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150 related items for PubMed ID: 6980184

  • 21. Roles of reactive nitrogen intermediates and transforming growth factor-beta produced by immunosuppressive macrophages in the expression of suppressor activity against T cell proliferation induced by TCR stimulation.
    Shimizu T, Cai S, Tomioka H.
    Cytokine; 2005 Apr 07; 30(1):7-13. PubMed ID: 15784407
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  • 22. Resting B cells from autoimmune lupus-prone New Zealand Black and (New Zealand Black x New Zealand White)F1 mice are hyper-responsive to T cell-derived stimuli.
    Jongstra-Bilen J, Vukusic B, Boras K, Wither JE.
    J Immunol; 1997 Dec 15; 159(12):5810-20. PubMed ID: 9550377
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  • 23. Autoimmunity develops in lupus-prone NZB mice despite normal T cell tolerance.
    Wither J, Vukusic B.
    J Immunol; 1998 Nov 01; 161(9):4555-62. PubMed ID: 9794382
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  • 24. The mechanism of nasal tolerance in lupus prone mice is T-cell anergy induced by immature B cells that lack B7 expression.
    Wu HY, Monsonego A, Weiner HL.
    J Autoimmun; 2006 Mar 01; 26(2):116-26. PubMed ID: 16426816
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  • 25. Exogenous hepatitis B surface antigen particles processed by dendritic cells or macrophages prime murine MHC class I-restricted cytotoxic T lymphocytes in vivo.
    Böhm W, Schirmbeck R, Elbe A, Melber K, Diminky D, Kraal G, van Rooijen N, Barenholz Y, Reimann J.
    J Immunol; 1995 Oct 01; 155(7):3313-21. PubMed ID: 7561024
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  • 26. Fibroblast-secreted macrophage colony-stimulating factor is responsible for generation of biphenotypic B/macrophage cells from a subset of mouse B lymphocytes.
    Borrello MA, Phipps RP.
    J Immunol; 1999 Oct 01; 163(7):3605-11. PubMed ID: 10490953
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  • 27. The role of suppressor T cells in the expression of autoimmune haemolytic anaemia in NZB mice.
    Russell PJ, Cunningham J, Dunkley M, Wilkinson NM.
    Clin Exp Immunol; 1981 Sep 01; 45(3):496-503. PubMed ID: 6461447
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  • 28. Augmentation of in vitro interleukin 10 production after in vivo administration of interleukin 18 is activated macrophage-dependent and is probably not involved in the antitumor effects of interleukin 18.
    Micallef MJ, Tanimoto T, Kohno K, Ikeda M, Ikegami H, Kurimoto M.
    Anticancer Res; 1998 Sep 01; 18(6A):4267-74. PubMed ID: 9891477
    [Abstract] [Full Text] [Related]

  • 29. Mechanism of action of macrophage-derived suppressor factor produced by soluble immune response suppressor-treated macrophages.
    Aune TM, Pierce CW.
    J Immunol; 1981 Jul 01; 127(1):368-72. PubMed ID: 7016995
    [Abstract] [Full Text] [Related]

  • 30. Activation of autoreactive T-cell clones from NZB.H-2bm12 mice.
    Naiki M, Yoshida SH, Ansari AA, Bill J, Gershwin ME.
    J Autoimmun; 1994 Jun 01; 7(3):275-90. PubMed ID: 7916904
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  • 33. Aberrant antigen presentation by macrophages from tumor-bearing mice is involved in the down-regulation of their T cell responses.
    Watson GA, Lopez DM.
    J Immunol; 1995 Sep 15; 155(6):3124-34. PubMed ID: 7673727
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  • 34. Regulation of murine macrophage phagocytosis of sheep erythrocytes by T-2 toxin.
    Corrier DE, Holt PS, Mollenhauer HH.
    Am J Vet Res; 1987 Aug 15; 48(8):1304-7. PubMed ID: 3631723
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  • 35. The role of antigen-presenting cells in the regulation of delayed-type hypersensitivity. II. Epidermal Langerhans' cells and peritoneal exudate macrophages.
    Morikawa Y, Furotani M, Matsuura N, Kakudo K.
    Cell Immunol; 1993 Nov 15; 152(1):200-10. PubMed ID: 8242760
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  • 39. The contribution of H-2bm12 and non H-2 background genes on murine lupus in NZB.H-2bm12/b mice.
    Watanabe Y, Yoshida SH, Ansari AA, Gershwin ME.
    J Autoimmun; 1994 Apr 15; 7(2):153-64. PubMed ID: 8037836
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