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Induction of natural IgE by glucocorticoids
Authors:Jaechul Lim  Erica V. Lin  Jun Young Hong  Bharat Vaidyanathan  Steven A. Erickson  Charles Annicelli  Ruslan Medzhitov
Affiliation:1. Department of Immunobiology, Yale University School of Medicine, New Haven, CT ; 2. Department of Systems Biology, College of Life Science and Biotechnology, Yonsei University, Seoul, South Korea ; 3. Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT
Abstract:IgE mediates allergic responses by coating mast cell or basophil surfaces and inducing degranulation upon binding a specific allergen. IgE can also be spontaneously produced in the absence of foreign allergens; yet the origin, regulation, and functions of such “natural” IgE still remain largely unknown. Here, we find that glucocorticoids enhance the production of IgE in B cells both in vivo and ex vivo without antigenic challenge. Such IgE production is promoted by B cell–intrinsic glucocorticoid receptor signaling that reinforces CD40 signaling and synergizes with the IL-4/STAT6 pathway. In addition, we found that rare B cells in the mesenteric lymph nodes are responsible for the production of glucocorticoid-inducible IgE. Furthermore, locally produced glucocorticoids in the gut may induce natural IgE during perturbations of gut homeostasis, such as dysbiosis. Notably, mice preemptively treated with glucocorticoids were protected from subsequent pathogenic anaphylaxis. Together, our results suggest that glucocorticoids, classically considered to be broadly immunosuppressive, have a selective immunostimulatory role in B cells.
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