Immune Responses to Fed Protein Antigens in Mice. 3. Systemic Tolerance or Priming Is Related to Age at Which Antigen Is First Encountered
暂无分享,去创建一个
[1] H. Drummond,et al. Immunological responses to fed protein antigens in mice. II. Oral tolerance for CMI is due to activation of cyclophosphamide-sensitive cells by gut-processed antigen. , 1983, Immunology.
[2] M. Arakawa,et al. Carrier-induced T helper and T suppressor cells involved in the regulation of hapten-specific DTH responses. , 1982, Journal of immunology.
[3] D. Hanson. Ontogeny of orally induced tolerance to soluble proteins in mice. I. Priming and tolerance in newborns. , 1981, Journal of immunology.
[4] A. Pesce,et al. Immunological properties of peptic fragments of bovine serum albumin. , 1979, Immunology.
[5] H. Etlinger,et al. Maturation of the lymphoid system. I. Induction of tolerance in neonates with a T-dependent antigen that is an obligate immunogen in adults. , 1979, Journal of immunology.
[6] N. Vaz,et al. Inhibition of specific immune responses by feeding protein antigens. , 1979, International archives of allergy and applied immunology.
[7] W. Walker,et al. Antigenicity of infant formulas: role of immature intestine on protein permeability. , 1978, The Journal of pediatrics.
[8] L. S. Kind,et al. Suppressor T cells for IgE and IgG in Peyer's patches of mice made tolerant by the oral administration of ovalbumin. , 1978, Journal of immunology.
[9] N. Vaz,et al. Inhibition of homocytotropic antibody responses in adult inbred mice by previous feeding of the specific antigen. , 1977, The Journal of allergy and clinical immunology.
[10] W. Ptak,et al. FETAL SUPPRESSOR CELLS: THEIR INFLUENCE ON THE CELL‐MEDIATED IMMUNE RESPONSES , 1977, Transplantation.
[11] A. Ferguson,et al. HYPERSENSITIVITY REACTIONS IN THE SMALL INTESTINE , 1977, Cell and tissue kinetics.
[12] C. Cambiaso,et al. A mechanism for the induction of immunological tolerance by antigen feeding: antigen-antibody complexes , 1975, The Journal of experimental medicine.
[13] R. Russell,et al. Pre- and postweaning disaccharidase patterns in isografts of fetal mouse intestine. , 1973, Gastroenterology.
[14] A. Ferguson,et al. The effect of antigen deprivation on thymus-dependent and thymus-independent lymphocytes in the small intestine of the mouse. , 1972, Clinical and experimental immunology.
[15] H. Cottier,et al. MAGNITUDE AND PATTERN OF THYMIC LYMPHOCYTE MIGRATION IN NEONATAL MICE , 1972, The Journal of experimental medicine.
[16] J. Chiller,et al. Cellular events during induction of immunologic unresponsiveness in adult mice. , 1971, Journal of immunology.
[17] F. W. Brambell. The transmission of immunity from mother to young and the catabolism of immunoglobulins. , 1966, Lancet.
[18] F. Dixon,et al. THE NATURE OF THE IMMUNOLOGIC INADEQUACY OF NEONATAL RABBITS , 1959, The Journal of experimental medicine.
[19] S. L. Clark. The Ingestion of Proteins and Colloidal Materials by Columnar Absorptive Cells of the Small Intestine in Suckling Rats and Mice , 1959, The Journal of biophysical and biochemical cytology.
[20] R. Billingham,et al. Acquired tolerance of foreign cells in newborn animals , 1956, Proceedings of the Royal Society of London. Series B - Biological Sciences.
[21] H. Drummond,et al. Immunological responses to fed protein antigens in mice. I. Reversal of oral tolerance to ovalbumin by cyclophosphamide. , 1982, Immunology.
[22] T. Tomasi. Oral tolerance. , 1980, Transplantation.
[23] M. Kagnoff. Effects of antigen-feeding on intestinal and systemic immune responses. IV. Similarity between the suppressor factor in mice after erythrocyte-lysate injection and erythrocyte feeding. , 1980, Gastroenterology.
[24] K. Isselbacher,et al. Uptake and transport of macromolecules by the intestine. Possible role in clinical disorders. , 1974, Gastroenterology.
[25] M. Parrott,et al. The induction of tolerance to a soluble protein antigen by oral administration. , 1974, Immunology.
[26] H. Cottier,et al. Thymic origin of lymphocytes in developing Peyer's patches of newborn mice. , 1971, Nature: New biology.