The IgE Antibody Response to the Phosphorylcholine Hapten

References

• Katz D. H. Recent studies on the regulation of IgE antibody synthesis in experimental animal and man. Immunology 1980; 41: 1
   PubMedGoogle Scholar
• Ishizaka K. Regulation of the IgE response by IgE-binding factors. Monogr. Allergy 1983; 18: 62
   Google Scholar
• Liu F.-T., Katz D. H. Immunological tolerance to allergic protein determinants: A therapeutic approach for selective inhibition of IgE antibody production. Proc. Natl. Acad. Sci. USA 1979; 76: 1430
   Google Scholar
• Sehon A. H. Suppression of IgE antibody responses with tolerogenic conjugates of allergens and haptens. Progr. Allergy 1982; 32: 161
   PubMedGoogle Scholar
• Blaser K., de Weck A. L. Regulation of the IgE antibody response by idiotype-antiidiotype network. Progr. Allergy 1982; 32: 203
   Google Scholar
• Blaser K., Wetterwald A., Weber E., Gerber V. E., de Weck A. L. Immune networks in immediate type allergic diseases. Ann. NY Acad. Sci 1983; 418: 330
   Google Scholar
• Blaser K., de Weck A. L. Regulation of the IgE-antibody response by complementary idiotypes. Immunohemotherapy, U. Nydegger. Academic Press, London 1981; 85
   Google Scholar
• Weber E., Blaser K. Suppression of the anti-BPO IgE response with hapten-modified spleen cells
   Google Scholar
• Kishimoto T., Hirai Y., Suemura M., Yamamura Y. Regulation of antibody response in different immunoglobulin classes. I. Selective suppression of anti-DNP IgE antibody response by preadministration of DNP-coupled mycobacterium. J. Immunol 1976; 117: 396
   Google Scholar
• Kishimoto T., Hirai Y., Nakamishi K., Azuma I., Nagamatsu A., Yamamura Y. Regulation of the antibody response immunoglobulin classes. VI. Selective Suppression of the IgE response by administration of antigen-conjugated muramyl-peptides. J. Immunol 1979; 123: 2709
   PubMedGoogle Scholar
• Tomasz A. A choline in the cell wall of a bacterium: a novel type of polymer linked in pneumococcus. Science 1967; 157: 694
   PubMedGoogle Scholar
• Potter M. Antigen-binding myeloma proteins in mice. Ann. NY Acad. Sci 1971; 190: 306
   Web of Science ®Google Scholar
• Leon M. A., Young N. M. Specificity for phosphorylcholine of six murine myeloma proteins reactive with pneumococcus C polysaccharide and β-lipoprotein. Biochemistry 1981; 10: 1424
   Google Scholar
• Claflin J. L., Liebermann R., Davie J. M. Clonal nature of the immune response to phosphorylcholine. II. Idiotypic specificity and binding characteristics of anti-phosphorylcholine antibodies. J. Immunol 1974; 112: 1747
   Google Scholar
• Claflin J. L., Culberley M. Clonal nature of the immune response to phosphorylcholine. VI. Molecular uniformity of a single idiotype among BALB/c mice. J. Immunol 1978; 121: 1410
   PubMedGoogle Scholar
• Gearhart P. J., Sigal N. H., Klinman N. R. Heterogeneity of the BALB/c antiphosphorylcholine response at the precursor cell level. J. Exp. Med 1975; 141: 56
   Google Scholar
• Gearhart P. J., Johnson N. D., Douglas R., Hood L. IgG antibodies to phosphorylcholine exhibit more diversity their IgM counterparts. Nature 1981; 291: 29
   PubMed Web of Science ®Google Scholar
• Chang S. P., Mc-Brown K., Rittenberg M. B. Immunologic memory to phosphorylcholine in vitro I. Asymetric expression of clonal dominance. J. Immunol 1981; 126: 975
   PubMedGoogle Scholar
• Chang S. P., Mc-Brown K., Rittenberg M. B. Immunologic memory to phosphorylcholine. II. PC-KLH induces two populations that dominate different isotypes. J. Immunol 1982; 128: 702
   Google Scholar
• Chang S. P., Mc-Brown K., Rittenberg M. B. Immunologic memory to phosphorylcholine. III. IgM includes a fine-specificity population distinct from TEPC-15. J. Immunol 1982; 128: 1559
   Google Scholar
• Heusser Ch., Bews J. P. A., Aebersold R., Blaser K. Antiphosphorylcholine antibodies with a preferred reactivity for either PC or PC-phenyl represent independent expression. Ann. Immunol. Inst. Pasteur 1984; 135C: 123
   Google Scholar
• Chang S. P., Perlmutter R. M., McBrown K., Heusser Ch., Hood L., Rittenberg M. B. Immunologic memory to phosphorylcholine. IV. Hybridomas representative of group I (T15 like) and group II (non-T15 like) antibodies utilize distinct VH genes. J. Immunol 1984; 132: 1550
   Google Scholar
• Todd I. S., Chang P., Perlmutter R. M., Aebersold R., Heusser Ch., Hood L., Rittenberg M. B. Immunologic memory to phosphorylcholine. V. Hybridomas representative of group II antibodies utilize VK 1–3 gene(s). J. Immunol 1984; 132: 1556
   Google Scholar
• Heusser Ch., Gisler R. H., Blaser K. Isolation and characterization of mouse IgE hybridoma against phosphorylcholine. Immunobiol 1981; 160: 43
   Google Scholar
• Blaser K., Heusser Ch. Regulatory effects of isologous anti-idiotypic antibodies on the formation of different immunoglobulin classes in the immune response to phosphorylcholine in BALB/c mice. Eur. J. Immunol 1984; 14: 93
   Google Scholar
• Blaser K., Nakagawa T., de Weck A. L. Suppression of the benzylpenicilloyl(BPO)-specific IgE formation with isologous anti-idiotypic antibodies in BALB/c mice. J. Immunol 1980; 125: 24
   Google Scholar
• Wetterwald A., Toffler O., de Weck A. L., Blaser K. Suppression of established IgE antibody responses with isologous anti-idiotypic antibodies in guinea pigs. Mol. Immunol 1986; 23: 347
   Google Scholar
• Blaser K., Geiser M., de Weck A. L. Suppression of phosphorylcholine-specific IgE antibody formation in BALB/c mice by isologous anti-T15 antiserum. Eur. J. Immunol 1979; 9: 1017
   Google Scholar
• Cerny J., Wallich R., Hämmerling G. J. Analysis of T15 idiotopes by monoclonal antibodies. Variability of idiotopic expression on phosphorylcholine-specific lymphocytes from individual inbred mice. J. Immunol 1982; 128: 1885
   Google Scholar
• Sakato N., Eisen H. N. Antibodies to idiotypes of isologous immunoglobulins. J. Exp. Med 1975; 141: 1411
   PubMed Web of Science ®Google Scholar
• Ishizaka K. Cellular events in the IgE antibody response. Adv. Immunol 1976; 23: 1
   PubMed Web of Science ®Google Scholar
• Hamaoka T., Katz D. H., Benacerraf B. Hapten-specific IgE antibody responses in mice. II. Cooperative interactions between adoptively transferred T and B lymphocytes in the development of IgE response. J. Exp. Med 1973; 138: 538
   Google Scholar
• Kishimoto T., Ishizaka K. Regulation of the antibody response in vitro IV. Carrier-specific helper cells for IgG and IgE antibody response. J. Immunol 1973; 117: 720
   Google Scholar
• Dessein A., Ju S. T., Dorf M. E., Benacerraf B., Germain R. N. IgE response to synthetic polypeptide antigen. II. Idiotype analysis of the IgE response to L-glutamic acid, L-alanine, L-tyrosine (GAT). J. Immunol 1980; 124: 71
   Google Scholar
• Hirano T., Kojima S., Hirayama N., Nelles M. J., Inada T., Nisonoff A., Ovary Z. Presence of an intrastrain idiotype on A/J antibodies of the IgE class specific for the p-azophenyl-arsonate group. J. Immunol 1983; 130: 1300
   Google Scholar
• Shigemoto S., Kishimoto T., Yamamura Y. Characterization of phosphorylcholine (PC) specific IgE B cells in CBA/N or ‘CBA/N × BALB/c’ F1 male mice. Eur. J. Immunol 1981; 127: 1070
   Google Scholar
• Haba S., Inada T., Nisonoff A. Quantitative measurements of cross-reactive idiotype in IgE antibodies. J. Mol. Immunol 1984; 73: 97
   Google Scholar
• Briles D. E., Formon C., Hudak S., Claflin J. L. Antiphosphorylcholine antibodies of the T15 idiotype are optimally protective against Streptococcus pneumoniae. J. Exp. Med 1982; 156: 1177
   PubMed Web of Science ®Google Scholar
• Karol R. A., Reichlin M., Nobel R. W. Evolution of an idiotypic determinant: anti-Val. J. Exp. Med 1977; 146: 436
   Google Scholar
• Jackson S., Kulhavy R., Mestecky J. Shared idiotypes among anti-albumin antibodies of different species. Scand. J. Immunol 1981; 14: 31
   Google Scholar
• Kabat E. A. Idiotypic determinants, minigenes and the antibody combining site. The Biology of Idiotypes, M. I. Green, A. Nisonoff. Plenum Press, New York 1984; 3
   Google Scholar
• Hirai Y., Lamoyi E., Dohi Y., Nisonoff A. Regulation of expression of a family of cross-reactive idiotypes. J. Immunol 1981; 126: 71
   Google Scholar
• Rothstein T. L., Margolies M. N., Getter M. L., Marshak-Rothstein A. Fine-specificity of idiotype suppression in A/J anti-azophenylarsonate response. J. Exp. Med 1983; 157: 795
   PubMed Web of Science ®Google Scholar
• Heusser Ch., Poskocil S., Julius M. H. A major idiotype (MI-1) on T15 positive B and T cells. Immunobiology 1980; 157: 227
   Google Scholar