Mechanism of the Immunoregulatory Effect of Cloned t Cells on Proliferation in Mixed Lymphocyte Responses

References

• Smith J B, DeHoratius R J. Deficient autologous mixed lymphocyte culture reaction correlates with disease activity in systemic lupus erythematosus and rheumatoid arthritis. Clin Exp Immunol 1982; 47: 155–62
   PubMedGoogle Scholar
• Sakane T, Steinberg A D, Green I. Failure of autologous mixed lymphocyte reactions between T and non-T cells in patients with systemic lupus erythematosus. Proc Natl Acad Sci. USA 1978; 75: 3464–68
   PubMedGoogle Scholar
• Miyasaka N, Sauvezie B, Pierce D A, Daniels T E, Talal N. Decreased autologous mixed lymphocyte reaction in Sjogrens syndrome. J Clin Invest 1980; 66: 928–33
   PubMed Web of Science ®Google Scholar
• Smith J B, Knowlton R P, Koons L S. Immunological studies in chronic lymphocytic leukemia: defective stimulation of T cell proliferation in autologous mixed lymphocyte culture. J Natl Cancer Inst 1977; 58: 579–85
   PubMed Web of Science ®Google Scholar
• Engleman E G, Benike C J, Hoppe R T, Kaplan H S, Berberich F R. Autologous mixed lymphocyte reaction in patients with Hodgkin's disease. Evidence for a T cell defect. J Clin Invest 1980; 66: 149–58
   PubMedGoogle Scholar
• Davey F R, Dock N L, Wolos J A. Studies of lymphocyte proliferation in hairy cell leukemia: Activity in mixed lymphocyte reaction and responses to mitogens. Br J Haematol 1980; 45: 29–39
   PubMedGoogle Scholar
• Yu D TY, Chiorazzi N., Kunkel H G. Helper factors derived from autologous mixed lymphocyte cultures. Cell Immunol 1980; 50: 305–13
   PubMed Web of Science ®Google Scholar
• Wolos J A, Smith J B. Helper cells in the autologous mixed lymphocyte reaction. I. Generation of cytotoxic T cells recognizing modified self H-2. J Immunol 1981; 127: 711–15
   PubMedGoogle Scholar
• Wolos J A, Smith J B. Helper cells in the autologous mixed lymphocyte reaction. III. Production of helper factor(s) distinct from IL-2. J Exp Mat 1982; 156: 1807–20
   PubMed Web of Science ®Google Scholar
• Chiorazzi N, Fu S M, Kunkel H G. Induction of polyclonal antibody synthesis by human allogeneic and autologous helper factors. J Exp Med 1980; 149: 1543–48
   Google Scholar
• Smith J B, Wolos J A, Bocchieri M H. Mechanisms of help and suppression in the AMLR: studies in normal and NZB mice. Behring Inst Mitt 1983; 72: 37–46
   Google Scholar
• Fitzharris P, Knight R A. Generation of suppressor cells in the autologous mixed lymphocyte reaction. Clin Exp Immunol 1981; 46: 185–95
   PubMedGoogle Scholar
• James S P, Yenokida G G, Graeff A S, Elson C O, Strober W. Immunoregulatory function of T cells activated in the autologous mixed lymphocyte reaction. J Immunol 1981; 127: 2605–09
   PubMed Web of Science ®Google Scholar
• Wolos J A, Spagnoli B, Smith J B. Suppression of a polyclonal B-cell response by supernatants from the murine autologous mixed lymphocyte reaction. Cell Immunol 1985; 96: 61–70
   PubMedGoogle Scholar
• Bonomo A C, El-Cheikh M C, Borojevic R, Cavalcante L A, Dos Reis G A. Comparative analysis of splenic cell proliferation induced by interleukin 3 and by syngeneic accessory cells (syngeneic mixed leukocyte reaction): Evidence that autoreactive T-cell functioning instructs hematopoietic phenomena. Cell Immunol 1990; 125: 210–24
   PubMedGoogle Scholar
• Nagarkatti P, Nagarkatti M, Kaplan A M. Normal Lytl1 2 T cells have the unique capacity to respond to syngeneic autoreactive T cells. J Exp Med 1985; 162: 375–80
   PubMed Web of Science ®Google Scholar
• Hausman P B, Stobo J D. Specificity and function of a human autologous reactive T cell. J Exp Med 1979; 149: 1537–42
   PubMedGoogle Scholar
• Faherty D A, Johnson D R, Zauderer M. Origin and specificity of autoreactive T cells in antigen-induced populations. J Exp Med 1985; 161: 1293–1301
   PubMed Web of Science ®Google Scholar
• Zauderer M, Campbell H, Johnson D R, Seman M. Helper functions of antigen-induced specific and autoreactive T cell colonies. J Mol Cell Immunol 1984; 1: 65–73
   PubMedGoogle Scholar
• Clayberger C, Dekruyff R H, Cantor H. Immunoregulatory activities of autoreactive T cells: An I-A specific T cell clone mediates both help and suppression of antibody responses. J Immunol 1984; 132: 2237–43
   PubMed Web of Science ®Google Scholar
• Glimcher L H, Shevach E M. Production of autoreactive I region restricted T cell hybridomas. J Exp Med 1982; 156: 640–45
   PubMed Web of Science ®Google Scholar
• Bocchieri M H. T-suppressor clones derived from murine AMLR. Immunology 1985; 56: 93–102
   PubMedGoogle Scholar
• Bocchieri M H. Immunoregulatory effects of cloned T cells on B-cell responses: comparison of autoimmune and non-autoimmune derived clones. Immunology 1989; 66: 526–31
   PubMedGoogle Scholar
• Mosmann T. Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays. J Immunol Methods 1983; 65: 55–63
   PubMed Web of Science ®Google Scholar
• Flood P M, Waltenbaugh C, Tada T, Chue B, Murphy D B. Serologic heterogeneity in I-J determinants associated with functionally distinct T cell regulatory factors. J Immunol 1986; 137: 2237–44
   PubMedGoogle Scholar
• Cuturi M C, Murphy M, Costa-Giomi M P, Weinmann R, Perussia B, Trinchieri G. Independent regulation of tumour necrosis factor and lymphotoxin production by human peripheral blood lymphocytes. J Exp Med 1987; 165: 1581–94
   PubMed Web of Science ®Google Scholar
• Sung S J, Bjorndahl J M, Wang C Y, Kao H T, Fu S M. Production of tumour necrosis factor/cachectin by human T cell lines and peripheral blood T lymphocytes stimulated by phorbol myristate acetate and anti-CD3 antibody. J Exp Med 1988; 937–53
   PubMedGoogle Scholar
• Kobayashi Y, Asada M, Osawa T. Production of lymphotoxin and tumour necrosis factor by a T-cell hybridoma. Immunology 1987; 60: 213–17
   PubMedGoogle Scholar
• Rubin B Y, Anderson S L, Sullivan S A, Williamson S D, Carswell E A, Old L J. Nonhematopoietic cells selected for resistance to tumour necrosis factor produce tumour necrosis factor. J Exp Med 1986; 164: 1350–55
   PubMed Web of Science ®Google Scholar
• Dayer J M, Beutler B, Cerami A. Cachectin/tumour necrosis factor stimulates collagenase and prostaglandin E2 production by human synovial cells and dermal fibroblasts. J Exp Med 1985; 162: 2163–68
   PubMed Web of Science ®Google Scholar
• Le J, Weinstein D, Gubler Y, Vilcek J. Induction of membrane-associated interleukin 1 by tumour necrosis factor in human fibroblasts. J Immunol 1987; 138: 2137–42
   PubMed Web of Science ®Google Scholar
• Scheurich P, Thomas B, Ucer U, Pfizenmaier K. Immunoregulatory activity of recombinant human tumour necrosis factor (TNF) alpha: Induction of TNF receptor on human T cells and TNF alpha-mediated enhancement of T cell responses. J Immunol 1987; 138: 1786–90
   PubMed Web of Science ®Google Scholar
• Shalaby M R, Espevik T, Rice G C, Ammann A J, Figari I S, Ranges G E, Palladino M A, JR. The involvement of human tumour necrosis factors alpha and beta in the mixed lymphocyte reaction. J Immunol 1988; 141: 499–503
   PubMedGoogle Scholar
• Kehri J H, Miller A, Fauci A S. Effect of tumour necrosis factor alpha on mitogen-activated human B cells. J Exp Med 1987; 166: 786–91
   PubMedGoogle Scholar
• Philip R, Epstein L B. Tumour necrosis factor as im-munodulator and mediator of monocyte cytoxicity induced by itself, gamma interferon and interleukin I. Nature 1986; 323: 86–89
   PubMed Web of Science ®Google Scholar
• Gifford G, Lohmann-Matthes M-L. Gamma interferon priming of mouse and human macrophages for induction of tumour necrosis factor production by bacterial lipopolysacch-aride. J Natl Cancer Inst 1987; 781: 121–24
   Google Scholar
• Lattime E C, Gillis S, Pecoraro G, Stutman O. la dependent interleukin-2 production in syngeneic cellular interactions. J Immunol 1982; 128: 480–85
   PubMed Web of Science ®Google Scholar