Abstract
Both experiments in rodents and experiments of nature in man suggest that isotypic regulation of the IgE response and its suppression represent a normal state of regulation. Accordingly, the abnormally elevated production of IgE to ubiquitous allergens, as observed in atopic people, might represent to some extent a breakdown of suppression and the expression of a state of partial immunodeficiency. Recent studies by several groups suggest that the isotypic regulation of IgE production is operated at several levels:
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a)
a network of T/B cell interactions in which non IgE-binding factors are produced by T and B cells (D. H. Katz);
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b)
IgE-binding molecules produced by T cells controlling the production/secretion of IgE by IgE-bearing B cells (several groups);
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c)
glycosylation-regulating factors which influence the enhancing or suppressing activity of IgE binding factors (K. Ishizaka).
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© 1986 Springer-Verlag Berlin Heidelberg
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de Weck, A.L., Stadler, B., Knutti-Müller, J. (1986). Regulation of IgE by Lymphoid Cell-Derived Factors. In: Ring, J., Burg, G. (eds) New Trends in Allergy II. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-71316-3_3
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DOI: https://doi.org/10.1007/978-3-642-71316-3_3
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