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Original Article

Experimental Hypersensitivity Pneumonitis: Suppressor Cell Influences

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Pages 903-921 | Received 12 May 1990, Accepted 10 Oct 1990, Published online: 02 Jul 2009

References

  • Schuyler M, Salvaggio J. Hypersensitivity pneumonitis. In Seminars in Respiratory Medicine 1984; 5: 246–254
  • Pepys J. Hypersensitivity diseases of the lung due to fungi and organic dusts. Monograph Allergy 1984; 4: 1–145
  • Keller R, Swartz S, Schleuter D, Bar-Sela S, Fink J. Immunoregulation in hypersensitivity pneumonitis: phenotypic and functional studies of bronchoalveolar lavage lymphocytes. Am Rev Resp Dis 1984; 130: 766–771
  • Keller R, Calvanico N, Stevens J. Hypersensitivity pneumonitis in non human primates. I. Studies on the relationship of immunoregulation and disease activity. J Immunol 1982; 128: 116–122
  • Asherson G, Colizzi V, Zembala M. An overview of T-suppressor cell circuits. Annu Rev Immunol 1986; 4: 37–68
  • Semenzato G, Agostini C, Sambello R, Trentin L, Chilosi M, Pizzolo G, Ciprian A. Lung T cells in hypersensitivity pneumonitis: phenotypic and functional analyses. J Immunol 1986; 137: 1164–1172
  • Sun D, Bin Y, Chluba J, Epplen J, Wekerle H. Suppression of experimentally induced autoimmune encephalomyelitis by cytolytic T-T interactions. Nature 1988; 332: 843–845
  • Caspi R, Kuwabara T, Nussenblatt R. Characterization of a suppressor cell line which downgrades experimental autoimmune uveoretinitis in the rat. J Immunol 1988; 140: 2579–2584
  • Swierkosz J, Swanborg R. Suppressor cell control of unresponsiveness to experimental allergic encephalomyelitis. J Immunol 1975; 115: 631–633
  • Welch A, Swanborg R. Characterization of suppressor cells involved in regulation of experimental allergic encephalomyelitis. Eur J Immunol 1976; 6: 910–914
  • Lider O, Santos L, Lee C, Higgins P, Weiner H. Suppression of experimental allergic encephalomyelitis by oral administration of myelin basic protein. J Immunol 1989; 142: 748–752
  • 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
  • Sakaguchi S, Fukuma K, Kuribayashe K, Masuda T. Organ specific autoimmune diseases induced in mice by elimination of T cell subset. J Exp Med 1986; 161: 72–87
  • Kelly C, Silvers W, Neilson E. Tolerance and parenchymal self. J Exp Med 1985; 162: 1892–1903
  • Sun D, Ben-Nun A, Wekerle H. Regulatory circuits in autoimmunity: recruitment of counter-regulatory CD8 + T cells by encephalitogenic CD4 + T line cells. Eur J Immunol 1985; 18: 1993–1999
  • Pelfrey C, Waxman F, Whitacre C. Genetic resistance in experimental allergic encephalomyelitis. I. Analysis of the mechanism of LeR resistance using radiation chimeras. Cell Immunol 1989; 122: 504–516
  • Schuyler M, Subramanyan S, Hassan M. Experimental hypersensitivity pneumonitis: transfer with cultured cells. J Lab Clin Med 1987; 109: 623–630
  • Schuyler M, Crooks L. Experimental hypersensitivity pneumonitis: kinetics and dose response. Am Rev Resp Dis 1989; 139: 996–1002
  • Schuyler M, Gott K, Shopp G, Crooks L. Experimental hypersensitivity pneumonitis: influence of donor sensitization. J Lab Clin Med 1990; 115: 621–628
  • Taurong J, Sandberg G, Mahowald M. The cellular basis of adjuvant arthritis. II. Characterization of the cells mediating passive transfer. Cell Immunol 1983; 80: 198–204
  • Caspi R, Roberge F, McAllister C, El-Saied M, Kuwabara T, Gery I, Hanna G, Nussenblatt R. T cell lines mediating experimental autoimmune uveoretinitis (EAU) in the rat. J Immunol 1986; 136: 928–933
  • Mahi-Brown C, Yule T, Tung K. Adoptive transfer of murine autoimmune orchitis to naive recipients with immune lymphocytes. Cell Immunol 1987; 106: 408–419
  • Holda J, Swanborg R. Autoimmune effector cells. II. Transfer of experimental allergic encephalomyelitis with a subset of T lymphocytes. Eur J Immunol 1982; 12: 453–455
  • Jarjour W, Asofsky R, Raine C, Stone S. Transfer of autoimmune encephalomyelitis with T lymphocytes in strain 13 guinea pigs. Cell Immunol 1986; 103: 462–468
  • Pettinelli C, McFarlin D. Adoptive transfer of experimental allergic encephalomyelitis in SJL/J mice after in vitro activation of lymph node cells by myelin basic protein: requirement for Lyt 1+2- T lymphocytes. J Immunol 1981; 127: 1420–1423
  • Lando S, Ben-Nun A. Experimental autoimmune encephalomyelitis mediated by T cell line. Clin Immunol Immunopathol 1984; 30: 303–310
  • Schluesener H, Wekerle H. Autoaggressive T lymphocyte lines recognizing the encephalitogenic region of myelin basic protein: in vitro selection from unprimed rat T lymphocyte populations. J Immunol 1985; 135: 3128–3133
  • Kira J, Itoyama Y, Goto I. Generation of CD4+ blastoid T cells showing marked upregulation of CD4, Class I and II MHC, and IL2 receptor molecules is required for the expression of potent encephalitogenicity. Cell Immunol 1989; 123: 264–275
  • Silberg D, Swanborg R. Autoimmune effector cells. VIII. Cellular requirements for the induction of autoreactive T cells of experimental allergic encephalomyelitis in non immune rats. J Immunol 1986; 136: 2432–2436
  • Kira J, Itoyama Y, Goto J. Relationship between surface marker expression and encephalitogenic potency of BP-cultured lymphocytes. Cell Immunol 1988; 112: 14–26
  • Kira J, Itoyama Y, Goto I. Surface phenotypic changes of spleen cells on acquisition of encephalitogenicity. J Neurimmunol 1987; 16: 365–379
  • Kurup V, Agre N. Transfer of Micropolyspora rectivirgula (Krassilnikov and Agre 1964) Lechevalier, Lechevalier, and Becker 1966 to Faeni gen. nov. Int J Systemic Bacteriol 1983; 33: 663–665
  • Blouin A, Cormier Y. Endotracheal intubation of guinea pigs by direct laryngoscopy. Lab Anim Sci 1987; 37: 244–245
  • Schuyler M, Cook C, Listrom M, Fenoglio-Preiser C. Blast cells transfer experimental hypersensitivity pneumonitis. Am Rev Resp Dis 1988; 137: 1449–1455
  • Kurnick J, Ostberg L, Stegagno M, Kimura A, Orn A, Sjoberg O. A rapid method for the separation of functional lymphoid cell populations of human and animal origin on PVP-silical (Percoll) density gradients. Scand J Immunol 1979; 10: 663–673
  • Cohn Z, Weiner E. The particulate hydrolases of macrophages. J Exp Med 1963; 188: 991–1003
  • Chiba J, Chused T, Leiserson W, Zweig S, Shevach E. Production and characterization of monoclonal antibodies to guinea pigs lymphoid differentiation antigens. J Immunol Methods 1983; 63: 247–261
  • Burger R, Scher I, Sharrow S, Shevach E. Non activated guinea pig T cells and thymocytes express Ia antigens: FACS analysis with alloantibodies and monoclonal antibodies. Immunol Today 1984; 51: 93–102
  • Feinberg S. Analysis of Cross-Classified Categorical Data, 2d ed. MIT Press, Cambridge, MA 1980; 23
  • Winer B J. Statistical Principles in Experimental Design, 2d ed. McGraw-Hill, New York 1971; 198
  • Baker D, Karcher K, Antoniou A, Turk J, Tan B, Scheper R. Changes in lymphocyte subsets after treatment with cyclophosphamide and during the development of contact sensitivity in the guinea pig. Int J Immunopharmacol 1987; 9: 175–183
  • Antoniou A, Parker D, Turk J, Tan B, Scheper R. Immunocytochemical identification and quantitation of mononuclear cells in the meninges during the development of chronic relapsing experimental allergic encephalomyelitis (CREAE) in the guinea pig. Cell Immunol 1986; 97: 386–396

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