Do Anergic T Cells Induce Suppressor T Lymphocytes Through Idiotypic Interactions?

References

• Eichman K., Falk I., Rajewsky K. Recognition of idiotype interactions. Eur. J. Immunol 1978; 8: 853–857
   Google Scholar
• Woodland R., Cantor H. Idiotype-specific T helper cells are Required to induce idiotype-positive B memory cells to secrete antibody. Eur. J. Immunol 1978; 8: 600–606
   Google Scholar
• Herzenberg L. A., Black S. J., Herzenberg L. A. Regulatory circuits and antibody Responses. Eur. J. Immunol 1980; 10: 1–11
   Google Scholar
• Cohen I. R., Atlan H. Network Recognition of autoimmunity in automaton model. Journal of Autoimmunity 1989; 2: 613–625
   PubMed Web of Science ®Google Scholar
• Pereira P., Bandeira A., Coutinho A., Marcos M. -A., Toribio M., Martinez C. A. V-region connectivity in T cell Repertoires. Ann. Rev. Immunol 1989; 7: 209–249
   Google Scholar
• Tse D. B., Al-Haideri M., Pernis B., Cantor C. R., Wang C. Y. Intracellular accumulation of T-cell Receptor complex molecules in a human T-cell line. Science 1986; 234: 748–751
   Google Scholar
• Kourilsky P., Chaouat G., Rabourdin-Combe C., Claverie J. M. Working principles in the immune system implied by the “peptide self” model. Proc. Natl. Acad. Sci. USA 1987; 84: 3400–3404
   PubMed Web of Science ®Google Scholar
• Batchelor J. R., Lombardi G., Lechler R. I. Speculation on the specificity of suppression. Immunology Today 1989; 10: 37–40
   Google Scholar
• Happ M. P., Heber-Katz E. Differences in the Repertoire of the Lewis rat T cell Response to self and non-self myelin basic proteins. J. Exp. Med 1988; 167: 502–513
   PubMed Web of Science ®Google Scholar
• Acha-Orbea H., Mitchell D. J., Timmerman L., Wraith D. C., Tausch G. S., Waldor M. K., Zamvil S. S., McDevitt H. O., Steinmann L. Limited heterogeneity of T cell Receptors from lymphocytes mediating autoimmune encephalomyelitis allows specific immune intervention. Cell 1988; 54(2)263
   Google Scholar
• Ben-Nun A., Wekerle H., Cohen I. Vaccination against autoimmune encephalomyelitis with T lymphocyte line cells Reactive against myelin basic protein. Nature 1981; 292: 60–63
   PubMed Web of Science ®Google Scholar
• Lider O., Reshef T., Beraud E., Ben-Nun A., Cohen I. Anti-idiotypic network induced by T cell vaccination against experimental autoimmune encephalomyelitis. Science 1988; 239: 181–183
   PubMed Web of Science ®Google Scholar
• Sun D., Qim Y., Chluba J., Epplen J. T., Wekerle H. Suppression of experimentally induced autoimmune encephalomyelitis by cytolytic T-T cell interactions. Nature 1988; 332: 843–845
   PubMed Web of Science ®Google Scholar
• Vandenbark A. A., Hashim G., Offner H. Immunization with a synthetic T-cell Receptor V-region peptide protects against experimental autoimmune encephalomyelitis. Nature 1989; 341: 541–544
   PubMed Web of Science ®Google Scholar
• Howell M. D., Winters S. T., Olee T., Powell H. C., Carlo D. J., Brostoff S. W. Vaccination against experimental allergic encephalomyelitis with T cell Receptor peptides. Science 1989; 246: 688
   Google Scholar
• Offner H., Hashim G. A., Vandenbark A. A. T cell Receptor peptide therapy triggers autoregulation of experimental encephalomyelitis. Science 1991; 251: 430
   PubMed Web of Science ®Google Scholar
• Jiang H., Sercarz E., Nitecki D., Pernis B. The problem of presentation of T cell Receptor peptides by activated T cells. N.Y. Acad. Sci 1991; 636: 28–32
   PubMedGoogle Scholar
• Minami Y., Weissman A. M., Samelson L. E., Klausner R. Building a multichain Receptor: Synthesis, degradation, and assembly of the T-cell antigen Receptor. Proc. Natl. Acad. Sci. USA 1987; 84: 2688–2692
   PubMed Web of Science ®Google Scholar
• Chen C., Bonifacino J. S., Yuan L. C., Klausner R. Selective degradation of T cell antigen Receptor chains Retained in a pre-Golgi compartment. J. Cell. Biol 1988; 107: 2149–2161
   Google Scholar
• Bonifacino J. S., Suzuki C. K., Lippincot-Schwartz J., Weissman A. M., Klausner R. Pre-Golgi degradation of newly synthesized T-cell antigen Receptor chains: Intrinsic sensitivity and Role of subunit assembly. J. Cell. Biol 1989; 109: 73–83
   PubMed Web of Science ®Google Scholar
• Tse D., Pernis B. Spontaneous internalization of class I MHC antigens in T lymphoid cells. J. Exp. Med 1984; 159: 193–207
   PubMedGoogle Scholar
• Tse D. B., Cantor C. R., McDowell J., Pernis B. Recycling class I MHC antigens: Dynamics of internalization, acidification and ligand-degradation in murine T lymphoblasts. J. Mol. Cell. Immunol 1986; 2: 315–329
   PubMedGoogle Scholar
• Yewdell J. W., Benninck J. R. Advances in Immunology 1992, in press
   Google Scholar
• Hochman J. H., Jiang H., Matyus L., Edidin M., Pernis B. Endocytosis and dissociation of class I MHC molecules labeled with fluorescent beta-2-microglobulin. J. Immunol 1991; 146: 1862–1867
   Google Scholar
• Hunt D. F., Henderson R. A., Shabanowitz J., Sakaguchi K., Michel H., Sevilir N., Cox A. L., Appella E., Engelhard V H. Characterization of peptides bound to class I MHC molecule HLA-A2.1 by mass spectrometry. Science 1992; 255: 1261–1263
   PubMed Web of Science ®Google Scholar
• Lamb J. R., Skidmore B. J., Green N., Chiller J. M., Feldmann M. Induction of tolerance in influenza virus immune T lymphocyte clones with synthetic peptides of influenza hemagglutinin. J. Exp. Med 1983; 157: 1434–1447
   PubMed Web of Science ®Google Scholar
• Lamb J. R., Zanders E. D., Sewell W., Crampton M. J., Feldmann M., Owen M. J. Antigen-specific T cell unresponsiveness in cloned helper T cells mediated via the CD2 or CD3/Ti Receptor pathways. Eur. J. Immunol 1987; 17: 1641–1644
   Google Scholar
• Jenkins M. K., Schwartz R. H. Antigen presentation by chemically modified splenocytes induces antigen-specific T cell unresponsiveness in vitro and in vivo. J. Exp. Med 1987; 165: 302–319
   PubMed Web of Science ®Google Scholar
• Quill H., Schwartz R. H. Stimulation of normal inducer T cell clones with antigen presented by purified la molecules in planar lipid membranes: specific induction of a long-lived state of proliferative nonresponsiveness. J. Immunol 1987; 138: 3704–3712
   PubMed Web of Science ®Google Scholar
• Rammensee H. G., Kroschewski R., Frangoulis B. Clonal anergy induced in mature VB6+ T lymphocytes on immunizing Mls-16 mice with Mls-la expressing cells. Nature 1989; 339: 541–544
   PubMed Web of Science ®Google Scholar
• Jenkins M. K., Pardoll D. M., Mizuguchi J., Chused T. M., Schwartz R. H. Molecular events in the induction of a non-responsive state in interleukin-2 producing helper T-lymphocyte clones. Proc. Natl. Acad. Sci. USA 1987; 84: 5409–5413
   PubMed Web of Science ®Google Scholar
• Go C., Miller J. Differential induction of transcription factors that Regulate the interleukin 2 gene during anergy induction and Restimulation. J. Exp. Med 1992; 175: 1325–1336
   Google Scholar
• Parker D. C., Eynon E. E. Antigen presentation in acquired immunological tolerance. FASEB Journal 1991; 5: 2777–2784
   Google Scholar
• Dorf M. E., Benacerraf B. Suppressor cells and immunoregulation. Ann. Rev. Immunol 1984; 2: 127–158
   PubMed Web of Science ®Google Scholar
• Ucker D. S. Cytoxic T lymphocytes and glucocorticoids activate an endogenous suicide process in target cells. Nature 1987; 327: 62–64
   PubMed Web of Science ®Google Scholar
• Salgame P., Modlin R., Bloom B. R. On the mechanism of human T cell suppression. Intl. Immunol 1989; 1: 121–129
   Google Scholar
• Jiang H., Zhang S. L., Pernis B. Role of CD8+ T cells in murine experimental allergic encephalomyelitis. Science 1992; 256: 1213–1215
   PubMed Web of Science ®Google Scholar
• Koh D. R., Fung-Leung W. P., Ho A., Gray D., Acha-Orbea H., Mak T. W. Less mortality but more Relapses in experimental allergic encephalomyelitis in CD8+ mice. Science 1992; 256: 1210–1213
   PubMed Web of Science ®Google Scholar
• Ohmori K., Hong Y., Fujiwara M., Matsumoto Y. In situ demonstration of proliferating cells in the Rat central nervous system during experimental autoimmune encephalomyelitis. Evidence suggesting that most infiltrating T cells do not proliferate in the target organ. Laboratory Investigation 1992; 66: 54–62
   PubMedGoogle Scholar