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1039 related items for PubMed ID: 7687618

  • 1. Functionally anergic lpr and gld B220+ T cell receptor (TCR)-alpha/beta+ double-negative T cells express CD28 and respond to costimulation with phorbol myristate acetate and antibodies to CD28 and the TCR.
    Giese T, Allison JP, Davidson WF.
    J Immunol; 1993 Jul 15; 151(2):597-609. PubMed ID: 7687618
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  • 2. Cytokine secretion by C3H-lpr and -gld T cells. Hypersecretion of IFN-gamma and tumor necrosis factor-alpha by stimulated CD4+ T cells.
    Davidson WF, Calkins C, Hügins A, Giese T, Holmes KL.
    J Immunol; 1991 Jun 15; 146(12):4138-48. PubMed ID: 1674953
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  • 3. Evidence for early onset, polyclonal activation of T cell subsets in mice homozygous for lpr.
    Giese T, Davidson WF.
    J Immunol; 1992 Nov 01; 149(9):3097-106. PubMed ID: 1383337
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  • 4. In CD8+ T cell-deficient lpr/lpr mice, CD4+B220+ and CD4+B220- T cells replace B220+ double-negative T cells as the predominant populations in enlarged lymph nodes.
    Giese T, Davidson WF.
    J Immunol; 1995 May 15; 154(10):4986-95. PubMed ID: 7537297
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  • 5. Chronic treatment of C3H-lpr/lpr and C3H-gld/gld mice with anti-CD8 monoclonal antibody prevents the accumulation of double negative T cells but not autoantibody production.
    Giese T, Davidson WF.
    J Immunol; 1994 Feb 15; 152(4):2000-10. PubMed ID: 8120404
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  • 11. Distinct signal transduction in mouse CD4+ and CD8+ splenic T cells after CD28 receptor ligation.
    Abe R, Vandenberghe P, Craighead N, Smoot DS, Lee KP, June CH.
    J Immunol; 1995 Feb 01; 154(3):985-97. PubMed ID: 7822814
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  • 12. Simultaneous ligation of CD5 and CD28 on resting T lymphocytes induces T cell activation in the absence of T cell receptor/CD3 occupancy.
    Verwilghen J, Vandenberghe P, Wallays G, de Boer M, Anthony N, Panayi GS, Ceuppens JL.
    J Immunol; 1993 Feb 01; 150(3):835-46. PubMed ID: 7678624
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  • 13. TcR-alpha/beta(+) CD4(-)CD8(-) T cells in humans with the autoimmune lymphoproliferative syndrome express a novel CD45 isoform that is analogous to murine B220 and represents a marker of altered O-glycan biosynthesis.
    Bleesing JJ, Brown MR, Dale JK, Straus SE, Lenardo MJ, Puck JM, Atkinson TP, Fleisher TA.
    Clin Immunol; 2001 Sep 01; 100(3):314-24. PubMed ID: 11513545
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  • 14. B7 costimulates proliferation of CD4-8+ T lymphocytes but is not required for the deletion of immature CD4+8+ thymocytes.
    Tan R, Teh SJ, Ledbetter JA, Linsley PS, Teh HS.
    J Immunol; 1992 Nov 15; 149(10):3217-24. PubMed ID: 1385518
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  • 16. Ligation of the CD5 or CD28 molecules on resting human T cells induces expression of the early activation antigen CD69 by a calcium- and tyrosine kinase-dependent mechanism.
    Vandenberghe P, Verwilghen J, Van Vaeck F, Ceuppens JL.
    Immunology; 1993 Feb 15; 78(2):210-7. PubMed ID: 7682535
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  • 17. CD28 is an inducible T cell surface antigen that transduces a proliferative signal in CD3+ mature thymocytes.
    Turka LA, Ledbetter JA, Lee K, June CH, Thompson CB.
    J Immunol; 1990 Mar 01; 144(5):1646-53. PubMed ID: 2155264
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  • 20. Expansion of the population of double negative CD4-8- T alpha beta-cells in the liver is a common feature of autoimmune mice.
    Masuda T, Ohteki T, Abo T, Seki S, Nose S, Nagura H, Kumagai K.
    J Immunol; 1991 Nov 01; 147(9):2907-12. PubMed ID: 1833460
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