Effects of Iodide on Class II-MHC Antigen Expression in Iodine Deficient Hyperplastic Thyroid Glands

References

• Weetman A P, McGregor A M. Autoimmune thyroid disease: Developments in our understanding. Endocr Rev 1984; 5: 309–355
   PubMed Web of Science ®Google Scholar
• Fradkin J E, Wolf J. Iodide-induced thyrotoxicosis. Medicine 1983; 62: 1–20
   PubMed Web of Science ®Google Scholar
• Edmunds H T. Acute thyroiditis from potassium iodide. Br Med J 1955; Ia: 354
   Google Scholar
• Hall R, Turner-Warwick M, Doniach D. Autoantibodies in iodide goiter and asthma. Clin Exp Immunol 1966; 1: 285–296
   PubMedGoogle Scholar
• Harach H R, Escalante D A, Onativia A, Lederer Outes J, Doy E S, Saravia Day E, Williams E D. Thyroid carcinoma and thyroiditis in an endemic goiter region before and after iodine prophylaxis. Acta Endocrinol 1985; 108: 55–60
   PubMedGoogle Scholar
• Boukis M A, Koutras D A, Souvatzoglou A, Evangelopoulou A, Vrontakis M, Karaiskos K S, Piperingos G D, Kitsopanidis J, Moulopoulos S D. Iodine-induced autoimmunity. Thyroid disorders associated with iodine deficiency and excess, R Hall, J. Kobberling. Raven Press, New York 1985; 217–221
   Google Scholar
• Koutras D A, Karaikos K S, Evaneelo Doulou K, Boukis M A, Piperingos G D, Kitsopanides J, Makriyannis D, Mantzos J, Sfontouris J, Souvatzoglou A. Thyroid autoantibodies after iodine supplementation. The thyroid and autoimmunity, H A Drexhage, W M Wiersinga. Elsevier Science Publishers, Amsterdam 1986; 211–212
   Google Scholar
• Koutras D A, Karaiskos K S, Piperingos G D, Kitsopanides J, Boukis M A, Makriyannis D, Souvatzoglou A, Sfontouris J, Evangelopoulou K, Moulopoulos S D, Katsouyanni K, Trichopoulos D. Treatment of endemic goiter with iodine and thyroid hormones, alone or in combination. Endocrinologica experimentalis 1986; 20: 57–65
   PubMedGoogle Scholar
• Bagchi N, Brown T R, Urdanivia E, Sundick R S. Induction of autoimmune thyroiditis in chickens by dietary iodine. Science 1985; 230: 325–327
   PubMed Web of Science ®Google Scholar
• Sundick R S, Herdegen D, Brown T R., Bagchi N. Thyroiditis induced by dietary iodine may be due to the increased immunogenicity of highly iodinated thyroglobulin. The thyroid and autoimmunity, H A Drexhage, W M Wiersinga. Elsevier Science Publishers, Amsterdam 1986; 213–214
   Google Scholar
• Allen E M, Appel M C, Braverman L E. The efect of iodide ingestion on the development of spontaneous lymphocytic thyroiditis in the diabetes-Prone BB/W rat. Endocrinology 1986; 118: 1977–1981
   PubMed Web of Science ®Google Scholar
• Follis R H. Thyroiditis resulting from administration of excess iodine to hamsters with hyperplastic goiters. Proc Sot, Exp Med 1959; 102: 425–429
   PubMed Web of Science ®Google Scholar
• Follis R H. Further observations on thyroiditis and colloid accumulation in hyperplastic thyroid glands of hamsters receiving excess iodine. Lab Invest 1964; 13: 1590–1599
   PubMed Web of Science ®Google Scholar
• Many M C, Denef J F, Cathy P, Haumont S. Morphological and functional changes during thyroid hyperplasia and involution in C3H mice: Evidence for folliculoneogenesis during involution. Endocrinology 1983; 112: 1292–1302
   PubMed Web of Science ®Google Scholar
• Mahnioud I, Colin I, Many M C, Denef J F. Direct toxic effect of iodide in excess of iodine-deficient thyroid glands: Epithelial necrosis and inflammation associated with lipofuscin accumulation. Exp Mol Pathol 1986; 44: 259–271
   PubMed Web of Science ®Google Scholar
• Denef J F, Cordier A C, Mesquita M, Haumont S. The influence of fixation procedure, embedding medium and section thickness on morphometric data in thyroid gland. Histochemistry 1979; 63: 163–171
   PubMedGoogle Scholar
• Bhattacharya A, Dorf M E, Springer T A. A shared alloantigenic determinant on la antigens encoded by theI-Aand I-Esubregions: evidence for I region gene duplication. J Immunol 1981; 127: 2488–2495
   PubMed Web of Science ®Google Scholar
• Van Vliet E, Melis M, Van Ewijk W. Monoclonal antibodies to stromal cell types of the mouse thymus. Eur J Immunol 1984; 14: 524–529
   PubMed Web of Science ®Google Scholar
• Springer T, Galfre G, Secher D S, Milstein C. Mac-I: a macrophage differentiation antigen identified by monoclonal antibody. Eur J Immunol 1979; 9: 301–306
   PubMed Web of Science ®Google Scholar
• Ho M K, Springer T A. Mac-2. a novel 32.000 M, mouse macrophage subpopulation-specific antigen defined by monoclonal antibodies. J Immunol 1982; 128: 1221–1228
   PubMed Web of Science ®Google Scholar
• Kraal G, Breel M, Janse M, Brun G. Langerhans cells, veiled cells, and interdigitating cells in the mouse recognized by a monoclonal antibody. J Exp Med 1986; 163: 981–997
   PubMed Web of Science ®Google Scholar
• Breel M, Mebius R E, Kraal G. Dendritic cells of the mouse recognized by two monoclonal antibodies. Eur J Immunol 1987; 17: 1555–1559
   PubMed Web of Science ®Google Scholar
• Graham R C, Karnovsky M J. The early stages of absorption of injected horseradish peroxidase in the proximal tubules of mouse kidney: ultrastructural cytochemistry by a new technique. J Histochem Cytochem 1966; 14: 291–301
   PubMed Web of Science ®Google Scholar
• Kelly J, Whelan C A, Weir D G, Feighery C. Removal of endogenous peroxidase activity from cryostat sections for immunoperoxidase visualisation of monoclonal antibodies. J Immunol Meth 1987; 96: 127–132
   PubMed Web of Science ®Google Scholar
• Hart D N, Fabre J W. Demonstration and characterization of la-positive dendritic cells in the interstitial connective tissues of rat heart and other tissues, but not brain. J Exp Med 1981; 153: 347–361
   Google Scholar
• Hart D NJ, Newton M R, Reece-Smith H, Fabre J W, Morris P J. Major histocompatibility complex antigens in the rat pancreas, isolated pancreatic islets, thyroid, and adrenal. Transplantation 1983; 36: 431–435
   PubMed Web of Science ®Google Scholar
• Parr E L, Lafferty K J, Bowen K M, McKenzie I FC. H-2 complex and Ia antigens on cells dissociated from mouse thyroid glands and islets of Langerhans. Transplantation 1980; 30: 142–148
   PubMed Web of Science ®Google Scholar
• Kabel P J, Voorbij H AM, van der Gaag R D, Wiersinga W M., de Haan M, Drexhage H A. Dendritic cells in autoimmune thyroid disease. Acta Endocrinol 1987; 281(suppl)42–48
   Google Scholar
• Steinman R M, Cohn Z A. Identification of a novel cell type in peripheral lymphoid organs of mice. I. Morphology, quantification. tissue distribution. J ESP Med 1973; 137: 1142–1162
   Google Scholar
• Steinman R M, Van Voorhis W C, Spalding D M. Dendritic cells. Handbook of experimental immunology, D M Weir. Cellular Immunology, Blackwell Scientific Publications, Oxford 1986; Vol 2: 49.1–49.9
   Google Scholar
• Rhodes J M, Agger R. Comparison of membrane antigens of mouse dendritic cell types. Immunol Lett 1987; 16: 107–112
   PubMed Web of Science ®Google Scholar
• Drexhage H A, Mullink H., de Groot J., Clarke J, Balfour B M. A study of cells present in peripheral lymph of pigs with special reference to a type of cell resembling the Langerhans cell. Cell Tissue Res 1979; 202: 407–430
   PubMed Web of Science ®Google Scholar
• Nabarra B, Papiernik M. Phenotype of thymic stromal cells. An immunoelectron microscopic study with anti-IA, anti-MAC-I. and anti-MAC-2 antibodies. Lab Invest 1988; 58: 524–531
   PubMed Web of Science ®Google Scholar
• Flotte T J, Springer T A, Thorbecke G J. Dendritic cell and macrophage staining by monoclonal antibodies in tissue sections and epidermal sheets. Am J Pathol 1983; 111: 112–124
   PubMed Web of Science ®Google Scholar
• Van Ewijk W. Immunohistology of lymphoid and non-lymphoid cells in the thymus in relation to T lymphocytc differentiation. Am J Anat 1984; 170: 311–330
   PubMedGoogle Scholar
• Unanue E R, Allen P M. Comment on the finding of la expression in nonlymphoic cells. Lab Invest 1986; 55: 123–125
   PubMed Web of Science ®Google Scholar
• Wentworth P A, Ziegler H K. Induction of macrophage la expression by lipopolysaccharide and Listeria monocytogenes in congenitally athymic nude mice. J Immunol 1987; 138: 3167–3173
   PubMed Web of Science ®Google Scholar
• Lightman S, Palestine A G, Nussenblatt R B. lntraocular la expression in vivo induced in the absence of immune T cells. Cell Immunol 1987; 106: 242–249
   PubMed Web of Science ®Google Scholar
• Polman C H, Dijkstra C D, de Groot C JA, Koetsier J C, Sminia T. Presence of la-positive cells in the central nervous system of the rat during various pathological conditions. Int Archs Allergy appl Immun 1987; 83: 109–111
   PubMedGoogle Scholar
• Many M C, Denef J F, Hamudi S, Haumont S. Increased follicular heterogeneity in experimental colloid goiter produced by refeeding iodine excess after thyroid hyperplasia. Endocrinology 1986; 118: 637–644
   PubMed Web of Science ®Google Scholar
• Cohen S B, Weetman A P. Characterization of different types of experimental autoimmune thyroiditis in the Buffalo strain rat. Clin ESP Immunol 1987; 69: 25–32
   PubMed Web of Science ®Google Scholar
• Cohen S B, Dijkstra C D, Weetman A P. Sequential analysis of experimental autoimmune thyroiditis induced by neonatal thymectomy in the Buffalo strain rat. Cell Immunol 1988; 114: 126–136
   PubMed Web of Science ®Google Scholar
• Silberberg-Sinakin I, Thorbecke G J, Baer R L, Rosenthal S A, Berezowsky V. Antigen-bearing Langerhans cells in the skin dermal lymphatics and in lymph nodes. Cell Imniunol 1976; 25: 137–151
   PubMed Web of Science ®Google Scholar
• Lechler R I, Batchelor J R. Restoration of immunogenicity to passenger cell-depleted kidney allografts by the addition of donor strain dendritic cells. J ESP Med 1982; 155: 31–41
   Google Scholar
• Knight S C, Mertin J, Stackpoole A, Clark J. Induction of immune responses in vivo with small numbers of veiled (dendritic) cells. Proc Natl Acad Sci USA 1983; 80: 6032–6035
   PubMed Web of Science ®Google Scholar
• Poulter L W, Duke O, Hobbs S, Janossy G, Panayi G, Seymour G. The involvement of interdigitating (antigen-presenting) cells in the pathogenesis of rheumatoid arthritis. Clin Exp Immunol 1983; 51: 247–254
   PubMed Web of Science ®Google Scholar
• Wilders M M, Drexhage H A, Kokjé M, Verspaget H W, Meuwissen S GM. Veiled cells in chronic idiopathic inflammatory bowel disese. Clin Exp Immunol 1984; 55: 377–387
   PubMed Web of Science ®Google Scholar
• Kabel P J, Voorbij H AM, De Haan M., van der Gaag R D., Drexhage H A. Intrathyroidal dendritic cells. J Clin Endocrinol Metab 1988; 66: 199–207
   PubMed Web of Science ®Google Scholar
• Bottazzo G F, Pujol-Borrell R, Hanafusa T. Role of aberrant HLA-DR expression and antigen presentation in induction of endocrine autoimmunity. Lancet November, 1983; 12: 1115–1119
   Google Scholar