Abstract
We investigated the effect on specific antibody response of naive and sensitized mice orally administrated with low (0.25 mg) or high (10.0 mg) doses of Dermatophagoides pteronyssinus (Dp) extract. We also examined the effect of oral administration of Dp on the production of autoantibodies to immunoglobulin G (IgG) and immunoglobulin E (IgE). Naive and sensitized mice both showed a marked down-regulation of IgE antibody production, regardless of the dose of Dp. We also detected an inhibitory effect of the total IgE levels and the allergen-specific IgG1, IgG2a and IgG2b antibody response in sensitized mice given the low dose of Dp. In contrast, high doses of Dp stimulated IgG1 antibody production in both naive and sensitized animals. In addition, the oral tolerance induction protocol stimulated anti-F(ab')2gamma and anti-Fcgamma autoantibody production. Evaluation of IgG anti-IgE autoantibodies by a direct enzyme immunoassay (EIA) revealed the presence of these autoantibodies, predominantly of the IgG1 isotype, specifically in those animals fed with the high dose. In contrast, IgG-IgE complexes, determined by EIA using immobilized anti-IgE antibodies, were detected mainly in sera of control animals. The autoantibody anti-IgE specificity was tested against IgE-TNP and IgE-DANSYL murine proteins and revealed different inhibition profiles, suggesting the action of heterogeneous subpopulations of autoantibodies. Taken together, our results show that the oral tolerance protocol with Dp was able to modulate the production of allergen-specific IgE antibodies in both naive and sensitized animals. In addition, we suggest that anti-IgE autoantibodies participate in the modulation of allergic response triggered by oral tolerance protocols.
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Selected References
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- Boluda L., Berrens L. Do IgE-IgG complexes occur in the circulation? Clin Exp Immunol. 1995 Apr;100(1):145–150. doi: 10.1111/j.1365-2249.1995.tb03616.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Burstein H. J., Abbas A. K. In vivo role of interleukin 4 in T cell tolerance induced by aqueous protein antigen. J Exp Med. 1993 Feb 1;177(2):457–463. doi: 10.1084/jem.177.2.457. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chen S. S., Li Q., Pearlman E., Chen W. H. Dual mechanisms of potentiation of murine antigen-specific IgE production by cyclosporin A in vitro. J Immunol. 1992 Aug 1;149(3):762–767. [PubMed] [Google Scholar]
- Chen Y., Inobe J., Marks R., Gonnella P., Kuchroo V. K., Weiner H. L. Peripheral deletion of antigen-reactive T cells in oral tolerance. Nature. 1995 Jul 13;376(6536):177–180. doi: 10.1038/376177a0. [DOI] [PubMed] [Google Scholar]
- Chen Y., Kuchroo V. K., Inobe J., Hafler D. A., Weiner H. L. Regulatory T cell clones induced by oral tolerance: suppression of autoimmune encephalomyelitis. Science. 1994 Aug 26;265(5176):1237–1240. doi: 10.1126/science.7520605. [DOI] [PubMed] [Google Scholar]
- Friedman A., Weiner H. L. Induction of anergy or active suppression following oral tolerance is determined by antigen dosage. Proc Natl Acad Sci U S A. 1994 Jul 5;91(14):6688–6692. doi: 10.1073/pnas.91.14.6688. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Holt P. G., Batty J. E., Turner K. J. Inhibition of specific IgE responses in mice by pre-exposure to inhaled antigen. Immunology. 1981 Mar;42(3):409–417. [PMC free article] [PubMed] [Google Scholar]
- Inganäs M., Johansson S. G., Bennich H. Anti-IgE antibodies in human serum: occurrence and specificity. Int Arch Allergy Appl Immunol. 1981;65(1):51–61. doi: 10.1159/000232737. [DOI] [PubMed] [Google Scholar]
- Lens J. W., van den Berg W. B., van de Putte L. B., van den Bersselaar L. Flare-up of antigen-induced arthritis in mice after challenge with oral antigen. Clin Exp Immunol. 1984 Nov;58(2):364–371. [PMC free article] [PubMed] [Google Scholar]
- Melamed D., Friedman A. Direct evidence for anergy in T lymphocytes tolerized by oral administration of ovalbumin. Eur J Immunol. 1993 Apr;23(4):935–942. doi: 10.1002/eji.1830230426. [DOI] [PubMed] [Google Scholar]
- Mota I., Wong D. Homologous and heterologous passive cutaneous anaphylactic activity of mouse antisera during the course of immunization. Life Sci. 1969 Aug 15;8(16):813–820. doi: 10.1016/0024-3205(69)90099-x. [DOI] [PubMed] [Google Scholar]
- OVARY Z. Passive cutaneous anaphylaxis in the mouse. J Immunol. 1958 Oct;81(4):355–357. [PubMed] [Google Scholar]
- Scheuer A., Haas H., Schlaak M. Prevalence and subclass distribution of IgG-anti-IgE autoantibodies in atopy and parasitosis. Int Arch Allergy Appl Immunol. 1991;96(3):271–276. doi: 10.1159/000235506. [DOI] [PubMed] [Google Scholar]
- Shakib F., Powell-Richards A. Elucidation of the epitope locations of human autoanti-IgE: recognition of two epitopes located within the C epsilon 2 and the C epsilon 4 domains. Int Arch Allergy Appl Immunol. 1991;95(2-3):102–108. doi: 10.1159/000235413. [DOI] [PubMed] [Google Scholar]
- Shakib F., Smith S. J., Pritchard D. I. Do autoantibodies to IgE play a role in IgE-mediated events? Immunol Cell Biol. 1995 Apr;73(2):109–112. doi: 10.1038/icb.1995.18. [DOI] [PubMed] [Google Scholar]
- Stadler B. M., Stämpfli M. R., Miescher S., Furukawa K., Vogel M. Biological activities of anti-IgE antibodies. Int Arch Allergy Immunol. 1993;102(2):121–126. doi: 10.1159/000236561. [DOI] [PubMed] [Google Scholar]
- Van Ommen R., Vredendaal A. E., Savelkoul H. F. Secondary IgE responses in vivo are predominantly generated via gamma 1 epsilon-double positive B cells. Scand J Immunol. 1994 Nov;40(5):491–501. doi: 10.1111/j.1365-3083.1994.tb03495.x. [DOI] [PubMed] [Google Scholar]
- Vassella C. C., de Weck A. L., Stadler B. M. Natural anti-IgE auto-antibodies interfere with diagnostic IgE determination. Clin Exp Allergy. 1990 May;20(3):295–303. doi: 10.1111/j.1365-2222.1990.tb02687.x. [DOI] [PubMed] [Google Scholar]
- Weyer A., Le Mao J., Etievant M., David B., Guinnepain M. T., Saint-Remy J. M. Human auto-anti-idiotypic antibodies to mite-specific IgE can degranulate human basophils in vitro. Clin Exp Allergy. 1995 Oct;25(10):935–941. doi: 10.1111/j.1365-2222.1995.tb00395.x. [DOI] [PubMed] [Google Scholar]
- Whitacre C. C., Gienapp I. E., Orosz C. G., Bitar D. M. Oral tolerance in experimental autoimmune encephalomyelitis. III. Evidence for clonal anergy. J Immunol. 1991 Oct 1;147(7):2155–2163. [PubMed] [Google Scholar]
- Yu Y., de Weck A. L., Stadler B. M., Müller U. Anti-IgE autoantibodies and bee-sting allergy. Allergy. 1995 Feb;50(2):119–125. doi: 10.1111/j.1398-9995.1995.tb05067.x. [DOI] [PubMed] [Google Scholar]
- van Halteren A. G., van der Cammen M. J., Biewenga J., Savelkoul H. F., Kraal G. IgE and mast cell response on intestinal allergen exposure: a murine model to study the onset of food allergy. J Allergy Clin Immunol. 1997 Jan;99(1 Pt 1):94–99. doi: 10.1016/s0091-6749(97)70305-1. [DOI] [PubMed] [Google Scholar]
