Abstract
The proposition of Mackay and Burnet that failure of immune regulation is best envisaged as the central feature of autoimmune disease remains as relevant three decades later as it was in 1964. Nevertheless, views on the precise manner in which immune homeostasis is achieved have changed since then, accompanying changes in perception of the mechanisms mediating immune functions. It is likely that they will be subject to ongoing modification as understanding of the immune system is further refined.
Probably the most satisfactory way to look at autoimmune disease is as a failure at some point of the normal homeostatic mechanisms that prevent the emergence of forbidden clones (1).
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References
Mackay IR, Burnet, FM. Autoimmune diseases: pathogenesis, chemistry and therapy. C.C. Thomas. Springfield IL, 1964.
Nishizuka Y, Sakakura T. Thymus and reproduction: sex-linked dysgenesia of the gonad after neonatal thymectomy in mice. Science 1969;166:753–755.
Sakakura T, Nishizuka Y. Thymic control mechanism in ovarian development: reconstitution of ovarian dysgenesis in thymectomized mice by replacement with thymic and other lymphoid tissues. Endocrinology 1972;90:431–437.
Nishizuka Y, Sakakura T. Ovarian dysgenesis induced by neonatal thymectomy in the mouse. Endocrinology 1971; 89:886–893.
Biskind MS, Biskind GR. Development of tumors in rat ovary after transplantation into spleen. Proc Soc Exp Biol Med 1994;55:176–179.
Besedovsky H, Sorkin E. Network of immune-neuroendocrine interactions. Clin Exp Immunol 1977; 27:1–12.
Jones HW, HoerrnL, Osol A. Blakiston’ s New Gould Medical Dictionary. Blakiston, Philadelphia, PA, 1951.
Daniel PM, Excell BJ, Gale MM, Pratt OE. The drainage of thyroid hormone by the lymphatics of the thyroid gland. J Physiol 1961;160:6–7P.
Daniel PM, Gale MM, Pratt OE. Radioactive iodine in the lymph leaving the thyroid gland. Q J Exp Phyiol 1963;48:138–145.
Daniel PM, Gale MM, Pratt OE. Hormones and related substances in the lymph leaving four endocrine glands-the testis, ovary, adrenal and thyroid. Lancet 1963;i:1232–1234.
Lindner HR. Partition of androgen between the lymph and venous blood of the testis in the ram. J Endocrinol 1963;25:483–494.
Lindner HR, Sass MB, Morris B. Steroids in the ovarian lymph and blood of conscious ewes. J Endocrinol 1964;30:361–376.
Brezinschek HP, Faessler R, Klocker H, Kroemer G, Sgonc R, Dietrich H, et al. Analysis of the immuneendocrine feedback loop in the avian system and its alteration in chickens with spontaneous autoimmune thyroiditis. Eur J Immunol 1990;20:2155–2159.
Bernton EW, Beach JE, Holaday JW, Smalbridge RC, Fein HG. Release of multiple hormones by a direct action of interleukin-1 on pituitary cells. Science 1987;238:519–521.
Brown SL, Smith LR, Blalock JE. Interleukin 1 and interleukin 2 enhance propiomelanocortin gene expression in pituitary cells. J Immunol 1987;139:3181–3183.
Pierpaoli W, Besedovsky HO. Role of the thymus in programing of neuroendocrine functions. Clin Exp Immunol 1975;20:323–338.
Heijnen CJ, Bevers C, Kavelaars A, Ballicux RE. Effect of a-endorphin on the antigen-induced primary antibody response of human blood B cells in vitro. J Immunol 1986;136:213–216.
Mandler RN, Biddison WE, Mandler R, Serrate SA. β-endophin augments the cytolytic activity and interferon production of natural killer cells. J Immunol 1986;136:934–939.
Bhardwaj RS, Schwarz A, Becher E, Mahnke K, Aragane Y, Schwarz T, et al. Pro-opiomelanocortinderived peptides induce IL-10 production in human monocytes. J Immunol 1996;156:2517–2521.
Weisz-Carrington P, Roux ME, McWilliams M, Phillips-Quagliata JM, Lamm ME. Hormonal induction of the secretory immune system in the mammary gland. Proc Natl Acad Sci USA 1978;75: 2928–2932.
Larson DF. Mechanism of action: antagonism of the prolactin receptor. Prog Allergy 1986;38:222–238.
Hiestand PC, Mekler P, Nordmann R, Grieder A, Permmongkol C. Prolactin as a modulator of lymphocyte responsiveness provides a possible mechanism of action for cyclosporine. Proc Natl Acad Sci USA 1986;83:2599–2603.
Smith EM, Blalock JE. Human lymphocyte production of corticotrophin and endorphin-like substances: association with leukocyte interferon. Proc Natl Acad Sci USA 1981;78:7530–7534.
Smith EM, Phan M, Kruger TE, Coppenhaver DH, Blalock JE. Human lymphocyte production of immunoreactive thyrotrophin. Proc Natl Acad Sci USA 1983;80:6010–6013.
Kruger TE, Blalock JE. Cellular requirements for thyrotrophin enhancement of in vitro antibody production. J Immunol 1986;137:197–200.
Harbour-McMenamin D, Smith EM, Blalock JE. Production of immunoreactive chorionic gonadotrophin during mixed lymphocyte reactions: a possible selective mechanism for genetic diversity. Proc Natl Acad Sci USA 1986;83:1834–1838.
Paul WE, Seder RA. Lymphocyte responses and cytokines, Cell 1994;76:241–251.
Poo W-J, Conrad L, Janeway CA. Receptor-directed focusing of lymphokine release by helper T cells. Nature 1988;332:378–380.
Roitt IM, Hutchings PR, Dawe KJ, Sumar N, Bodman KB, Cooke A. The forces driving autoimmune disease. J Autoimmunity 1992;5(Suppl A):11–26.
Felten DL, Felten SY, Bellinger DL, Carlson SZ, Ackerman KD, Madden KS, et al. Noradrenergic sympathetic neural interacitons with the immune system: structure and function. Immun Rev 1987;100: 225–260.
Singh U. Effect of catecholamines on lymphopoiesis in fetal mouse thymic explants. J Anat 1979; 129:279–292.
Adams DD. The presence of an abnormal thyroid-stimulating hormone in the serum of some thyrotoxic patients. J Clin Endocrinol Metab 1958;18:699–712.
Pinchera A, Fenzi GF, Macchia E, Bartalena L, Mariotti S, Monzani F. Thyroid-stimulating immunoglobulins. Hormone Res 1982;16:317–328.
Ehrlich P. On immunity with special reference to cell life. Proc Roy Soc 1900;66:424–448.
Triplett EL. On the mechanism of immunologic self recognition. J Immunol 1962;89:505–510.
Bach J-F. Insulin-dependent diabetes mellitus as a β-cell targeted disease of immunoregulation. J Autoimmunity 1995;8:439–463.
Allison AC, Denman AM, Barnes RD. Cooperating and controlling functions of thymus-derived lymphocytes in relation to autoimmunity. Lancet 1971; ii:135–140.
Webb S, Morris C, Sprent J. Extrathymic tolerance of mature T cells: clonal elimination as a consequence of immunity. Cell 1990;63:1249–1256.
Morahan G, Allison J, Miller JFAP. Tolerance of class 1 histocompatibility antigens expressed extrathymically. Nature 1989;339:622–624.
Jolicoeur C, Hanahan D, Smith K. T-cell tolerance toward a transgenic β cell antigen and transcription of endogenous pancreatic genes in thymus. Proc Natl Acad Sci USA 1994;91:6707–6711.
Nossal GJV. Negative selection of lymphocytes. Cell 1994;76:229–239.
Janeway CA, Bottomly K. Signals and signs for lymphocyte responses. Cell 1994;76:275–285.
Weetman AP. Antigen presentation in the pathogenesis of autoimmune endocrine disease. J Autoimmunity 1995;8:305–312.
Todd I, Bottazzo GF. On the issue of inappropriate HLA class II expression on endocrine cells: an answer to a sceptic. J Autoimmunity 1995;8:313–322.
Chen Y, Kuchroo VK, Inobe J, Hafler DA, Weiner HL. Regulatory T cell clones induced by oral tolerance: suppression of autoimmune encephalomyelitis. Science 1994;265:1237–1240.
Miller A, Lider O, Roberts AB, Sporn MB, Weiner HL. Suppressor T cells generated by oral tolerization to myelin basic protein suppress both in vitro and in vivo immune responses by the release of transforming growth factor β after antigen-specific triggering. Proc Natl Acad Sci USA 1992;89:421–425.
Pontes de Carvalho LC, Templeman J, Wick G, Roitt IM. The role of self-antigen in the development of autoimmunity in obese strain chickens with spontaneous autoallergic thyroiditis. J Exp Med 1982; 155:1255–1265.
Larger E, Becourt C, Bach JF, Boitard C. Pancreatic islet β cells drive T cell-immune responses in the nonobese diabetic mouse model. J Exp Med 1995;181:1635–1642.
Sakaguchi S, Takahashi T, Nishizuka Y. Study on cellular events in post-thymectomy autoimmune oophoritis in mice. II Requirement of Lyt-1 cells in normal female mice. J Exp Med 1982;156: 1577–1586.
Chen X, Shelton J, McCullagh P. Suppression of anti-thyrocyte autoreactivity by the lymphocytes of normal fetal lambs. J Autoimmunity 1995;8:539–559.
Welch P, Rose NR, Kite JH. Neonatal thymectomy increases spontaneous autoimmune thyroiditis. J Immunol 1973;110:575–577.
Penhale WJ, Farmer A, McKenna RP, Irvine WJ. Spontaneous thyroiditis in thymectomized and irradiated Wistar rats. Clin Exp Immunol 1973;15:225–236.
Penhale WJ, Irvine WJ, Inglis JR, Farmer A. Thyroiditis in T cell-depleted rats: supression of the autoallergic response by reconstitution with normal lymphoid cells. Clin Exp Immunol 1976;25:6–16.
Sakaguchi N, Miyai K, Sakaguchi S. Ionizing radiation and autoimmunity. Induction of autoimmune disease in mice by high dose fractionated total lymphoid irradiation and its prevention by inoculating normal T cells. J Immunol 1994;152:2586–2596.
Stumbles PA, Penhale WJ. IDDM in rats induced by thymectomy and irradiation. Diabetes 1993;42: 571–578.
Sakaguchi S, Toda M, Asano M, Itoh M, Morse SS, Sakaguchi N. T cell-mediated maintenance of natural self-tolerance: its breakdown as a possible cause of various autoimmune diseases. J Autoimmunity 1996;9:211–220.
Fowell D, McKnight AJ, Powrie F, Dyke R, Mason D. Subsets of CD4+ T cells and their roles in the induction and prevention of autoimmunity. Immunol Rev 1991;123:37–63.
Sakaguchi S, Sakaguchi N, Asano M, Itoh M, Toda M. Immunologic self-tolerance maintained by activated T cells expressing IL-2 receptor a-chains (CD25). Breakdown of a single mechanism of selftolerance causes various autoimmune diseases. J Immunol 1995;155:1151–1164.
Oldstone MBA. Prevention of type 1 diabetes in nonobese diabetic mice by virus infection. Science 1988;239:500–502.
Rollins-Smith LA, Cohen N. Self-pituitary grafts are not rejected by frogs deprived of their pituitary anlagen as embyos. Nature 1982;299:820–821.
McCullagh P. Interception of the development of self tolerance in fetal lambs. Eur J Immunol 1989;19:1387–1392.
Eishi Y, McCullagh P. Acquisition of immunological self-recognition by the fetal rat. Immunology 1988;64:319–323.
McCullagh P. Curtailment of autoimmunity following parabiosis with a normal partner. Immunology 1990;71:595–597.
Chen X, McCullagh P. Expression and regulation of anti-thyroid autoimmunity directed against cultvated rat thyrocytes. J Autoimmunity 1995;8:521–538.
McCullagh P. The inability of thyroid allografts to induce self tolerance of organ-specific antigens in fetal lambs. Immunology 1991;72:405–410.
King KJ, Hagan RP, Mieno M, McCullagh P. Cellular interactions during the development of autoimmunity in a fetal lamb model of self-antigen deprivation. Clin Immunol Immunopath 1997;88:56–64.
Yoshikawa N, Morita T, Reseltkova E, Arreanza G, Carayon P, Volpe R. Reduced activation of suppressor T lymphocytes by antigens in autoimmune thyroid disease. J Endocrinol Invest 1993;16:609–617.
McCullagh P. The significance of immune suppression in normal self tolerance. Immunol Rev 1996;149:127–153.
Lou Y-H, McElVeen F, Adams S, Tung KSK. Altered target organ. A mechanism of postrecovery resistance to murine autoimmune oophoritis. JImmunol 1995;155:3667–3673.
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McCullagh, P. (1999). Immunoregulation in Experimental Autoimmune Endocrine Disease. In: Volpé, R. (eds) Autoimmune Endocrinopathies. Contemporary Endocrinology, vol 15. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-59259-704-8_2
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DOI: https://doi.org/10.1007/978-1-59259-704-8_2
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