Abstract
The antigen-induced secretion of the chemical mediators histamine and slow-reacting substance of anaphylaxis (SRS-A) has been detected in human lung tissue from asthmatic patients (Brocklehurst, 1960). These same chemical mediators are also released from human lung tissue obtained from normal individuals after passive sensitization with sera from allergic patients and challenge with specific antigen (Sheard et al., 1967; Parish, 1967). The antigen-antibody initiated secretory mechanism is modulated by a variety of hormones, which affect the intracellular levels of cyclic nucleotides (Orange et al., 1971a; Kaliner et al., 1972; Tauber et al., submitted for publication). These findings suggest that the subpopulation of target cells involved in the immunologic release of chemical mediators have specific receptors for alpha and beta adrenergic, cholinergic, and prostaglandin hormones as well as for IgE antibody. Although the hormones noted above can themselves stimulate secretion in some tissues, in the reaction to be considered, they modulate the secretory process stimulated by antigen-antibody interaction, instead.
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Kaliner, M., Austen, K.F. (1974). Hormonal Control of the Immunologic Release of Histamine and Slow-Reacting Substance of Anaphylaxis from Human Lung. In: Braun, W., Lichtenstein, L.M., Parker, C.W. (eds) Cyclic AMP, Cell Growth, and the Immune Response. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-86026-3_13
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DOI: https://doi.org/10.1007/978-3-642-86026-3_13
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