3-Methylcholanthrene-Induced Immunosuppression in Mice to Trichinella Spiralis Antigens

References

• Unanue E. R., Allen P. M. The basis for the immunoregulatory role of macrophages and other accessory cells. Science 1987; 236: 551
   PubMed Web of Science ®Google Scholar
• Unanue E. R., Beller D. I., Lu C. Y., Allen P. M. Opinion: Antigen presentation: comments on its regulation and mechanism. J. Immunol. 1984; 132: 1
   PubMed Web of Science ®Google Scholar
• Zedeck M. S. Polycyclic aromatic hydrocarbons: A review. J. Environ. Path. Toxicol. 1980; 3: 537
   PubMed Web of Science ®Google Scholar
• Kimura S., Gonzalez F. J., Nebert D. W. The murine Ahlocus. J. Biol. Chem. 1984; 259: 10705
   PubMed Web of Science ®Google Scholar
• Conney A. H. Induction of microsomal enzymes by foreign chemicals and carcinogens by polycyclic aromatic hydrocarbons: G.H.A. Clowes Memorial Lecture. Cancer Res. 1982; 42: 4875
   PubMed Web of Science ®Google Scholar
• Brookes P., Lawley P. D. Evidence for the binding of polynuclear aromatic hydrocarbons to the nucleic acids of mouse skin: relation between carcinogenic power of hydrocarbons and their binding to deoxyribonucleic acid. Nature (Lond.) 1964; 202: 781
   PubMed Web of Science ®Google Scholar
• Nebert D. W., Jensen N. M. The Ah locus: Genetic regulation of the metabolism of carcinogens, drugs, and other environmental chemicals by cytochrome P450-mediated monooxygenases. CRC Critical Reviews in Biochemistry, G. D. Fasman. CRC Press, Cleveland, OH 1979; Vol. 6.: 401–437
   Google Scholar
• Stjernsward J. Immunodepressive effect of 3-methylcholanthrene. Antibody formation at the cellular level and reaction against weak antigenic homografts. J. Natl. Cancer Inst. 1965; 35: 885
   Google Scholar
• Stjernsward J. Effect of non carcinogenic and carcinogenic hydrocarbons on antibody-forming cells measured at the cellular level in vitro. J. Natl. Cancer Inst. 1966; 36: 1189
   PubMed Web of Science ®Google Scholar
• Dean J. H., Luster M. I., Boorman G. A., Lauer L. D., Leubke R. W., Lawson L. Selective immunosuppression resulting from exposure to the carcinogenic congener of benzopyrene in B6C3F1 mice. Clin. Exp. Immunol. 1983; 53: 199
   Google Scholar
• White K. L., Holsapple M. P. Direct suppression of in vitro antibody production by mouse spleen cells by the carcinogen benzo(a)pyrene but not by the noncarcinogenic congener Benzo(e)pyrene. Cancer Res. 1984; 44: 3388
   PubMed Web of Science ®Google Scholar
• White K. L., Lysy H. H., Holsapple M. P. Immunosuppression by polycyclic aromatic hydrocarbons: A structure-activity relationship in B6C3F1 and DBA/2 mice. Immunopharmacol. 1985; 9: 155
   PubMed Web of Science ®Google Scholar
• Yamashita U., Hamaoka T. Selective suppression of host T cell and macrophage activities during 7. 12-dimethylbenz(a)anthracene-induced carcinogenesis. Gann 1982; 73: 773
   Google Scholar
• Blanton R. H., Lyte M., Myers M. J., Bick P. H. Immunomodulation by polyaromatic hydrocarbons in mice and murine cells. Cancer Res. 1986; 46: 2735
   PubMed Web of Science ®Google Scholar
• Myers M. J., Schook L. B., Bick P. H. Mechanisms of Benzo(a)pyrene-induced modulation of antigen presentation. J. Pharmacol. Exp. Ther. 1987; 242: 399
   PubMed Web of Science ®Google Scholar
• Krco C. J., David C. S., Wassom D. W. Characterization of an in vitro proliferation response to solubilized Trichinella spiralis antigens: role of Ia antigens and Ly-1+ T cells. Cell. Immunol. 1982; 68: 359
   Google Scholar
• Johnson B. E., Dietert R. R., Wassom D. L. The relative importance of Ah versus H-2genotype on Trichinella resistance following exposure to 3-methylcholanthrene. Int. J. Immunopharmacol. 1989; 11: 217
   Google Scholar
• Jerrells T. R., Dean J. H., Richardson G. L., Herberman R. B. Depletion of monocytes from human peripheral blood mononuclear leukocytes: Comparison of the sephadex G-10 column method with other commonly used techniques. J. Immunol. Meth. 1980; 32: 11
   PubMed Web of Science ®Google Scholar
• Wassom D. L., Dougherty D. A., Krco C. J., David C. S. H-2-controlled. dose-dependent suppression of the response that expells adult Trichinella spiralis from the small intestine of mice. Immunol. 1984; 53: 811
   Google Scholar
• Gillis S., Ferm M. M., Ou W., Smith K. A. T cell growth factor: Parameters of production and a quantitative microassay for activity. J. Immunol. 1978; 120: 2027
   PubMed Web of Science ®Google Scholar
• Gillis S., Smith K. A. Long term culture of tumor-specific cytotoxic T cells. Nature 1977; 268: 154
   PubMed Web of Science ®Google Scholar
• Snedecor G. W., Cochran W. G. Statistical Methods, seventh edition. Iowa State Univ. Press, Ames Iowa 1980
   Google Scholar
• Shapiro H. M. Practical Flow Cytometry. Alan R. Liss, Inc., New York 1985
   Google Scholar
• Poland A. P., Glover E. Genetic expression of aryl hydrocarbon hydroxylase activity: induction of monooxygenase activities and cytochrome P-450 formation by 2, 3, 7, 8-TCDD in mice genetically “non-responsive” to other hydrocarbons. J. Biol. Chem. 1974; 249: 5599a
   PubMed Web of Science ®Google Scholar
• Poland A. P., Glover E. Comparison of 2, 3, 7, 8-tetrachlorodibenzo-p-dioxin, a potent inducer of aryl hydrocarbon hydroxylase, with 3-methylcholanthrene. Molec. Pharmacol. 1974; 10: 349b
   PubMed Web of Science ®Google Scholar
• Gonzalez F. J., Tukey R. H., Nebert D. W. Structural gene products of the Ah locus. Transcriptional regulation of cytochrome P-450 and P-450 mRNA levels by 3-methylcholanthrene. Molec. Pharmacol. 1984; 26: 117
   Google Scholar
• Nebert D. W., Negishi M., Lang M. A., Hjelmeland L. M., Eisen H. J. The Ah locus. a multigene family necessary for survival in a chemically adverse environment: Comparison with the immune system. Adv. Genet. 1982; 21: 1
   Google Scholar
• Tucker A. N., Vore S. J., Luster M. I. Suppression of B cell differentiation by 2, 3. 7, 8-tetrachlorodibenzo-p-dioxin. Molec. Pharmacol. 1986; 29: 372
   PubMed Web of Science ®Google Scholar
• Silkworth J. B., Antrim L. Relationship between Ah receptor-mediated polychlorinated biphenyl (PCB)-induced humoral immunosuppression and thymic atrophy. J. Pharmacol. Exp. Ther. 1985; 235: 606
   PubMedGoogle Scholar
• Luster M. I., Blank J. A., Dean J. H. Molecular and cellular basis of chemically induced immunotoxicity. Ann. Rev. Pharmacol. Toxicol. 1987; 27: 23
   PubMed Web of Science ®Google Scholar
• Palacios R. Concanavalin A triggers T lymphocytes by directly interacting with their receptors for activation. J. Immunol. 1982; 128: 337
   PubMed Web of Science ®Google Scholar
• Caldwell C. W., Maggi J., Henry L. B., Taylor H. M. Fluorescence intensity as a quality control parameter in clinical flow cytometry. Am. J. Clin. Pathol. 1987; 88(4)447
   Google Scholar