Effects of HgCl₂ on the Expression of Autoimmune Responses and Disease in Diabetes-Prone (DP) BB Rats

References

• Kosuda L. L., Bigazzi P. E. Chemical-induced autoimmunity. Experimental lmmunotoxicology, R. J. Smialowicz, M. P. Holsapple. CRC Press, Boca Raton, FLA 1996; 419–465
   Google Scholar
• Sapin C., Druet E., Druet P. Induction of anti-glomerular basement membrane antibodies in the Brown-Norway rat by mercuric chloride. Clin. exp. Immunol. 1977; 28: 173–179
   PubMed Web of Science ®Google Scholar
• Fukatsu A., Brentjens J. R., Killen P. D., Kleinman H. K., Martin G. R., Andres G. A. Studies on the formation of glomerular immune deposits in Brown Norway rats injected with mercuric chloride. Clin. Immunol. lmmunopathol 1987; 45: 35–47
   PubMedGoogle Scholar
• Henry G. A., Jarnot B. M., Steinhoff M. M., Bigazzi P. E. Mercury-induced renal autoimmunity in the MAXX rat. Clin. Immunol, lmmunopathol 1988; 49: 187–203
   PubMedGoogle Scholar
• Aten J., Veninga A., Bruijn J. A., Prins F. A., de Heer E., Weening J. J. Antigenic specificities of glomerular-bound autoantibodies in membranous glomerulopathy induced by mercuric chloride. Clin. Immunol. lmmunopathol 1992; 63: 89–102
   PubMedGoogle Scholar
• Druet E., Sapin C., Gunther E., Feingold N., Druet P. Mercuric chloride-induced anti-glomerular basement membrane antibodies in the rat. Genetic control. Eur. J. Immunol 1977; 7: 348–351
   PubMed Web of Science ®Google Scholar
• Pelletier L., Pasquier R., Rossert J., Druet P. HgCl2 induces nonspecific immunosuppression in Lewis rats. Eur. J. Immunol 1987; 17: 49–54
   PubMed Web of Science ®Google Scholar
• Pelletier L., Galceran M., Pasquier R., Ronco P., Verroust P., Bariety J., Druet P. Down modulation of Heymann's nephritis by mercuric chloride. Kidney Int. 1987; 32: 227–232
   PubMed Web of Science ®Google Scholar
• Pelletier L., Rossert J., Pasquier R., Villarroya H., Belair M-F, Vial M-C, Oriol R., Druet P. Effect of HgCl2 on experimental allergic encephalomyelitis in Lewis rats. HgCl2-induced down-modulation of the disease. Eur. J. Immunol 1988; 18: 243–247
   PubMed Web of Science ®Google Scholar
• Castedo M., Pelletier L., Rossert J., Pasquier R., Villaroya H., Druet P. Mercury-induced autoreactive anti-class II T cell line protects from experimental autoimmune encephalomyelitis by the bias of CD8+ antier-gotypic cells in Lewis rats. J. Exp. Med. 1993; 177: 881–889
   PubMed Web of Science ®Google Scholar
• Röcken M., Racke M., Shevach E. M. IL-4-induced immune deviation as antigen-specific therapy for inflammatory autoimmune disease. Immunol Today 1996; 17: 225–231
   PubMedGoogle Scholar
• Bigazzi P. E., Rose N. R. Animal models of autoimmunity. The Handbook of Experimental Immunology, 5th Ed., D. M. Weir, C Blackwell, L. A. Herzenberg, L. A. Herzenberg. Blackwell Scientific Publications, OxfordUK, xxx–xxx, in press
   Google Scholar
• Crisá L., Mordes J. P., Rossini A. A. Autoimmune diabetes mellitus in the BB rat. Diabete.s/Metabol Rev. 1992; 8: 9–37
   Google Scholar
• Rossini A. A., Greiner D. L., Friedman H. P., Mordes J. P. Immunopathogenesis of diabetes mellitus. Diabetes Rev. 1993; 1: 43–75
   Google Scholar
• Rajatanavin R., Appeal M. C, Reinhardt W., Alex S., Yang Y-N, Braverman L. E. Variable prevalence of lymphocytic thyroiditis among diabetes-prone sublines of BB/Wor rats. Endocrinology 1991; 128: 153–157
   PubMed Web of Science ®Google Scholar
• Zipris D., Greiner D. L., Malkani S., Whalen B., Mordes J. P., Rossini A. A. Cytokine gene expression in islets and thyroids of BB rats. IFN-γ and IL-12p40 mRNA increase with age in both diabetic and insulin-treated nondiabetic BB rats. J. Immunol 1996; 156: 1315–1321
   PubMed Web of Science ®Google Scholar
• Guberski D. L., Thomas V. A., Shek W. R., Like A. A., Handler E. S., Rossini A. A., Wallace J. E., Welsh R. M. Induction of type I diabetes by Kilham's rat virus in diabetes-resistant BB/Wor rats. Science 1991; 254: 1010–1013
   PubMed Web of Science ®Google Scholar
• Like A. A., Guberski D. L., Butler L. Influence of environmental viral agents on frequency and tempo of diabetes mellitus in BB/Wor rats. Diabetes 1991; 40: 259–262
   PubMed Web of Science ®Google Scholar
• Kosuda L. L., Greiner D. L., Bigazzi P. E. Mercury-induced renal autoimmunity. Changes in RT6+ T lymphocytes of “susceptible” and “resistant” rats. Environ. Health Persp. 1993; 101: 178–185
   PubMed Web of Science ®Google Scholar
• Bigazzi P. E. Autoimmune orchitis and thyroiditis. Meth. Enzymol 1988; 162: 461–478
   PubMed Web of Science ®Google Scholar
• Nakhooda A. F., Like A. A., Chappel C. I., Wei C-N, Marliss E. B. The spontaneously diabetic Wis-tar rat (the “BB” rat). Studies prior to and during development of the overt syndrome. Diabetologia 1978; 14: 199–207
   PubMed Web of Science ®Google Scholar
• McCoy J. P. J., Michaelson J. H., Bigazzi P. E. Anti-idiotypic immunity and autoimmunity: III. Investigations in human autoimmune thyroiditis. Life Sci. 1982; 32: 109–118
   Web of Science ®Google Scholar
• de Savigny D., Voller A. The communication of EL1SA data from laboratory to clinician. J. Immunoassay 1980; 1: 105–128
   PubMedGoogle Scholar
• Kosuda L. L., Wayne A., Nahounou M., Greiner D. L., Bigazzi P. E. Reduction of the RT6.2+ subset of T lymphocytes in BN rats with mercury-induced renal autoimmunity. Cell. Immunol. 1991; 135: 154–167
   PubMed Web of Science ®Google Scholar
• Kleinman H. K., McGarvcy M. L., Liotta L. A., Robey P. G., Tryggvason K., Martin G. R. Isolation and characterization of Type IV procollagen, laminin, and heparan sulfate proteoglycan from the EHS sarcoma. Biochem. 1982; 21: 6188–6193
   PubMed Web of Science ®Google Scholar
• Sasaki M., Kleinman H. K., Hubert H., Deutzmann R., Yamada Y. Laminin, a multidomain protein. J. Biol. Chem. 1988; 263: 16536–16544
   PubMed Web of Science ®Google Scholar
• Kosuda L. L., Hannigan M. O., Bigazzi P. E., Leif J. H., Greiner D. L. Thymus atrophy and changes in thymocyte subpopulations of BN rats with mercury-induced renal autoimmune disease. Autoimmunity 1996; 23: 77–89
   PubMed Web of Science ®Google Scholar
• Elder M., Maclaren N., Riley W., McConnell T. Gastric parietal cell and other autoantibodies in the BB rat. Diabetes 1982; 31: 313–318
   PubMed Web of Science ®Google Scholar
• Like A. A., Appel M. C, Rossini A. A. Autoantibodies in the BB/W rat. Diabetes 1982; 31: 816–820
   PubMed Web of Science ®Google Scholar
• Allen E. M., Appeal M. C., Braverman L. E. The effect 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
• Bazin H., Rousseaux J., Rousseaux-Prévost R., Platteau B., Querinjean P., Malache J. M., Delattnay T. Rat immunoglobulins. Rat hybrido-mas and rat monoclonal antibodies, H. Bazin. CRC Press, Boca Raton, FLA 1990; 5–42
   Google Scholar
• Manouvriez P., Nisol F., Delaunay T., Bazin H. Isotyping of rat monoclonal antibodies. Rat hybridomas and rat monoclonal antibodies, H. Bazin. CRC Press, Boca Raton, FLA 1990; 127–137
   Google Scholar
• Rossini A. A., Handler E. S., Mordes J. P., Greiner D. L. Human autoimmune diabetes mellitus: lessons from BB rats and NOD mice-Caveat Emptor. Clin. Immunol. Immunopathol. 1995; 74: 2–9
   PubMedGoogle Scholar
• Bigazzi P. E., Michaelson J. H., Potter N. T. Epibodies in autoimmunity: antisera against autoantibodies to the renal glomerular basement membrane react with idiotypes as well as with autoantigens. Autoimmunity 1989; 5: 3–16
   PubMed Web of Science ®Google Scholar
• Greiner D. L., Handler E. S., Nakano K., Mordes J. P., Rossini A. A. Absence of the RT-6 T cell subset in diabetes-prone BB/W rats. J. Immunol. 1986; 136: 148–151
   PubMed Web of Science ®Google Scholar
• Kosuda L. L., Hosseinzadeh H., Greiner D. L., Bigazzi P. E. The role of RT6+ T lymphocytes in mercury-induced renal autoimmunity: experimental manipulations of “susceptible” and “resistant” rats. J. Toxicol. Envir. Health 1994; 42: 303–321
   PubMed Web of Science ®Google Scholar
• Pelletier L., Rossert J., Pasquier R., Vial M. C., Druet P. Role of CD8+ T cells in mercury-induced autoimmunity or immunosuppression in the rat. Stand. J. Immunol. 1990; 31: 65–74
   PubMed Web of Science ®Google Scholar
• Rossert J., Pelletier L., Pasquier R., Villaroya H., Oriol R., Druet P. HgCl2-induced perturbation of the T cell network in experimental allergic encephalomyelitis. I In vitro characterization of T cells involved. Cell. Immunol. 1991; 137: 367–378
   PubMed Web of Science ®Google Scholar
• Pelletier L., Rossert J., Pasquier R., Villaroya H., Oriol R., Druet P. HgCl2-induced perturbation of the T cell network in experimental allergic encephalomyelitis. II. In vivo demonstration of the role of T suppressor and contrasuppressor cells. Cell. Immunol. 1991; 137: 379–388
   PubMed Web of Science ®Google Scholar
• Engvall E., Krusius T., Wewer U., Ruoslahti E. Laminin from rat yolk sac tumor: isolation, partial characterization, and comparison with mouse laminin. Arch. Biochem. 1983; 222: 649–656
   PubMed Web of Science ®Google Scholar
• Wewer U., Engvall E. Laminins. Meth. Enzvmol 1994; 245: 85–104
   PubMed Web of Science ®Google Scholar
• Bernard A., Lauwcrys R., Gengoux P., Mahieu P., Foidart J. M., Druet P., Weening J. J. Anti-laminin antibodies in Sprague-Dawley and Brown Norway rats chronically exposed to cadmium. Toxicol. 1984; 31: 307–313
   PubMed Web of Science ®Google Scholar
• Bigazzi P. E. Lessons from animal models: the scope of mercury-induced autoimmunity. Clin. Immunol. Immunopathol. 1992; 65: 81–84
   PubMedGoogle Scholar
• Al-Balaghi S., Möller E., Möller G., Abedi-Valugerdi M. Mercury induces polyclonal B-cell activation, autoantibody production and renal immune complex deposits in young (NZBxNZW)F1 hybrids. Eur. J. Immunol. 1996; 26: 1519–1526
   PubMed Web of Science ®Google Scholar
• Benbernou N., Matsiota-Bernard P., Guenounou M. Antisense oligonucleotides to interleukin-4 regulate IgE and IgG2a production by spleen cells from Nippostrongylus brasiliensis-infected rats. Eur. J. Immunol. 1993; 23: 659–663
   PubMed Web of Science ®Google Scholar
• Gracie J. A., Bradley J. A. Intcrleukin-12 induces interferon-γ-dependent switching of IgG alloantibody subclass. Eur. J. Immunol. 1996; 26: 1217–1221
   PubMed Web of Science ®Google Scholar
• Dubey C., Bellon B., Druet P. TH1 and TH2 dependent cytokines in experimental autoimmunity and immune reactions induced by chemicals. Eur. Cytokine Net. 1991; 2: 147–152
   PubMedGoogle Scholar
• Goldman M., Druet P., Glciclimann E. TH2 cells in systemic autoimmunity: insights from allogeneic diseases and chemically-induced autoimmunity. Immunol. Today 1991; 12: 223–227
   PubMedGoogle Scholar
• Pelletier L., Bellon B., Tournade H., Dubey C, Guery J. C, Saoudi A., Hirsch F., Druet P. Chemical-induced autoimmunity. Molecular Immunobiology of Self-Reactivity, C. A. Bona, A. K. Kaushik. Marcel Dekker, Inc., New York 1992; 315–353
   Google Scholar
• Saoudi A., Kuhn J., Huygen K., de Kozak Y., Velu T., Goldman M., Druet P., Bellon B. TH2 activated cells prevent experimental autoimmune uveoretinitis, a TH I-dependent autoimmune disease. Eur. J. Immunol. 1993; 23: 3096–3103
   PubMed Web of Science ®Google Scholar
• Burstein D., Mordes J. P., Greiner D., Stein D., Naka-Mura N., Handler E., Rossini A. Prevention of diabetes in the BB/Wor rat by a single transfusion of spleen cells. Parameters that affect the degree of protection. Diabetes 1989; 38: 24–30
   PubMed Web of Science ®Google Scholar
• Mordes J. P., Gallina D. L., Handler E. S., Greiner D. L., Nakamura N., Pelletier A., Rossini A. A. Transfusions enriched for W3/25+ helper/inducer T lymphocytes prevent spontaneous diabetes in the BB/W rat. Diabetologia 1987; 30: 22–26
   PubMed Web of Science ®Google Scholar
• Bellgrau D., Lagarde A-C. Cytotoxic T-cell precursors with low-level CD8 in the diabetes-prone Biobreeding rat: implications for generation of an autoimmune T-cell repertoire. Proc. Nat. Acad. Sci. USA 1990; 87: 313–317
   PubMed Web of Science ®Google Scholar
• Woda B. A., Padden C. Biobreeding/Worcester (BB/Wor) rats are deficient in the generation of functional cytotoxic T cells. J. Immunol. 1987; 139: 1514–1517
   PubMed Web of Science ®Google Scholar
• Plamondon C., Kottis V., Brideau C., Métroz-Dayer M-D., Poussier P. Abnormal thymocyte maturation in spontaneously diabetic BB rats involves the deletion of CD4-8+ cells. J. Immunol. 1990; 144: 923–928
   PubMed Web of Science ®Google Scholar
• Whalen B. J., Greiner D. L., Mordes J. P., Rossini A. A. Adoptive transfer of autoimmune diabetes mellitus to athymic rats: synergy of CD4+ and CD8+T cells and prevention by RT6+ T cells. J. Autoimm. 1994; 7: 819–831
   PubMed Web of Science ®Google Scholar
• Fowell D., Mason D. Evidence that the T cell repertoire of normal rats contains cells with the potential to cause diabetes. Characterization of the CD4+ T cell subset that inhibits this autoimmune potential. J. Exp. Med. 1993; 177: 627–636
   PubMed Web of Science ®Google Scholar
• Saoudi A., Bellon B., De Kozak Y., Kuhn J., Vial M-C, Thillaye B., Druet P. Prevention of experimental autoimmune uveoretinitis and experimental autoimmune pinealitis in (Lewis x Brown-Norway)F1 rats by HgCl2 injections. Immunology 1991; 74: 348–354
   PubMed Web of Science ®Google Scholar
• Druet P., Sheela R., Pelletier L. TH1 and TH2 lymphocytes in autoimmunity. Adv. Nephrol 1996; 25: 217–241
   PubMedGoogle Scholar