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469 related items for PubMed ID: 16162272

  • 21. Persistent production of TH2-type cytokines and polyclonal B cell activation after chronic administration of staphylococcal enterotoxin B in mice.
    Florquin S, Amraoui Z, Goldman M.
    J Autoimmun; 1996 Oct; 9(5):609-15. PubMed ID: 8933276
    [Abstract] [Full Text] [Related]

  • 22. Immunomodulation of experimental colitis: the role of NK1.1 liver lymphocytes and surrogate antigens--bystander effect.
    Shlomai A, Trop S, Gotsman I, Jurim O, Diment J, Alper R, Rabbani E, Engelhardt D, Ilan Y.
    J Pathol; 2001 Nov; 195(4):498-507. PubMed ID: 11745683
    [Abstract] [Full Text] [Related]

  • 23. 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
    [Abstract] [Full Text] [Related]

  • 24. In vivo analysis of a superantigen-induced T cell suppressor factor.
    Hu HL, Cornwell WD, Rogers TJ, Lin YS.
    Cell Immunol; 1996 Feb 01; 167(2):285-92. PubMed ID: 8603438
    [Abstract] [Full Text] [Related]

  • 25. An analysis of NK1.1+ subpopulations in immune spleen cells and cells infiltrating rejecting thyroid allografts.
    Warren HS, Jorgensen-Fry K, Skipsey LJ.
    Transplant Proc; 1992 Feb 01; 24(1):246-7. PubMed ID: 1531711
    [No Abstract] [Full Text] [Related]

  • 26. CD1-dependent natural killer (NK1.1(+)) T cells are required for oral and portal venous tolerance induction.
    Margenthaler JA, Landeros K, Kataoka M, Flye MW.
    J Surg Res; 2002 May 01; 104(1):29-35. PubMed ID: 11971674
    [Abstract] [Full Text] [Related]

  • 27. Memory T cell tolerance to superantigens is not due to increased susceptibility to apoptosis.
    Lee WT, Padmanabhan J, Cole-Calkins J.
    J Autoimmun; 1997 Aug 01; 10(4):357-65. PubMed ID: 9237799
    [Abstract] [Full Text] [Related]

  • 28. Induction of interstitial pneumonia in autoimmune mice by intratracheal administration of superantigen staphylococcal enterotoxin B.
    Shinbori T, Matsuki M, Suga M, Kakimoto K, Ando M.
    Cell Immunol; 1996 Dec 15; 174(2):129-37. PubMed ID: 8954612
    [Abstract] [Full Text] [Related]

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  • 30. Liver-associated lymphocytes expressing NK1.1 are essential for oral immune tolerance induction in a murine model.
    Trop S, Samsonov D, Gotsman I, Alper R, Diment J, Ilan Y.
    Hepatology; 1999 Mar 15; 29(3):746-55. PubMed ID: 10051476
    [Abstract] [Full Text] [Related]

  • 31. Regulation of antibody response in different immunoglobulin classes. II. Induction of in vitro IgE antibody response in murine spleen cells and demonstration of a possible involvement of distinct T-helper cells in IgE and IgG antibody responses.
    Kimoto M, Kishimoto T, Noguchi S, Watanabe T, Yamamura Y.
    J Immunol; 1977 Mar 15; 118(3):840-5. PubMed ID: 300389
    [Abstract] [Full Text] [Related]

  • 32. Staphylococcal enterotoxin B induces an early and transient state of immunosuppression characterized by V beta-unrestricted T cell unresponsiveness and defective antigen-presenting cell functions.
    Muraille E, De Smedt T, Andris F, Pajak B, Armant M, Urbain J, Moser M, Leo O.
    J Immunol; 1997 Mar 15; 158(6):2638-47. PubMed ID: 9058796
    [Abstract] [Full Text] [Related]

  • 33. Regulation of hapten-specific memory IgE responses induced in vitro. Requirement for both Thy-1+ AsGM1+ and Thy-1+ AsGM1- cells and for IFN-alpha and IL-4.
    Herrick CA, Carucci JA, Kleiner GI, Durkin HG.
    J Immunol; 1993 Oct 01; 151(7):3440-9. PubMed ID: 8104220
    [Abstract] [Full Text] [Related]

  • 34. Persistence of apoptosis-resistant T cell-activating dendritic cells promotes T helper type-2 response and IgE antibody production.
    Arques JL, Regoli M, Bertelli E, Nicoletti C.
    Mol Immunol; 2008 Apr 01; 45(8):2177-86. PubMed ID: 18237782
    [Abstract] [Full Text] [Related]

  • 35. Association of intermediate T cell receptor cells, mainly their NK1.1(-) subset, with protection from malaria.
    Weerasinghe A, Sekikawa H, Watanabe H, Mannoor K, Morshed SR, Halder RC, Kawamura T, Kosaka T, Miyaji C, Kawamura H, Seki S, Abo T.
    Cell Immunol; 2001 Jan 10; 207(1):28-35. PubMed ID: 11161450
    [Abstract] [Full Text] [Related]

  • 36. Depletion of activated Vbeta8+ T cells disrupts bispecific antibody directed antitumor immunity.
    McConnell EJ, McLemore EC, Talac R, Joshi L, Nelson H.
    J Surg Res; 2004 Nov 10; 122(1):103-12. PubMed ID: 15522322
    [Abstract] [Full Text] [Related]

  • 37. Characterization of anergy to the superantigen Staphylococcus enterotoxin B.
    Dannecker G, Schultz H, Mecheri S, Sappler G, Clarke K, Niethammer D, Hoffmann MK.
    Immunodeficiency; 1993 Nov 10; 4(1-4):137-9. PubMed ID: 8167688
    [Abstract] [Full Text] [Related]

  • 38. Lymphoid cell dependence of eosinophil response to antigen. VI. The effect of selective removal of T or B lymphocytes on the capacity of primed spleen cells to adoptively transferred immunity to tetanus toxoid.
    Ponzio NM, Speirs RS.
    Immunology; 1975 Feb 10; 28(2):243-51. PubMed ID: 1079015
    [Abstract] [Full Text] [Related]

  • 39. The dual phases of the response to neonatal exposure to a VH family-restricted staphylococcal B cell superantigen.
    Silverman GJ, Nayak JV, Warnatz K, Hajjar FF, Cary S, Tighe H, Curtiss VE.
    J Immunol; 1998 Nov 15; 161(10):5720-32. PubMed ID: 9820554
    [Abstract] [Full Text] [Related]

  • 40. Up-regulation of murine neonatal T helper cell responses by accessory cell factors.
    Adkins B, Ghanei A, Hamilton K.
    J Immunol; 1994 Oct 15; 153(8):3378-85. PubMed ID: 7930563
    [Abstract] [Full Text] [Related]

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