Abstract
Human rIL-4 is able to induce the expression of low-affinity receptors for IgE (Fc epsilon RL/CD23) on resting B lymphocytes, as determined by the binding of either the anti Fc epsilon RL/CD23-specific mAb 25 or IgE. Stimulation of B cells with insolubilized anti-IgM antibody increases the number of cells expressing Fc epsilon RL/CD23 upon culturing with IL-4 and enhances the level of Fc epsilon RL/CD23 expression on these cells. Fc epsilon RL/CD23 induction is specific for IL-4 since IL-1 alpha, IL-2, IFN-gamma, B cell-derived B cell growth factor (BCGF), and a low-molecular-weight BCGF were ineffective. IFN-gamma strongly inhibited the induction of Fc epsilon RL/CD23 by IL-4.
MeSH Terms
B-Lymphocytes/drug effects,metabolism
Cells, Cultured
Dose-Response Relationship, Drug
Growth Substances/pharmacology
Humans
Interferon-gamma/pharmacology
Interleukin-4
Interphase
Lymphokines/pharmacology
Receptors, Fc/biosynthesis
Receptors, IgE
Recombinant Proteins/pharmacology
Chemicals
Growth Substances
Lymphokines
Receptors, Fc
Receptors, IgE
Recombinant Proteins
Interleukin-4
Interferon-gamma
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Defrance T
Aubry J P
Rousset F
Vanbervliet B
Bonnefoy J Y
Arai N
Takebe Y
Yokota T
Lee F
Arai K
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