CD23 and its soluble components (sCD23) play an important role in IgE regulation. Sera of patients with atopic dermatitis (AD) were reported to contain an IgE-binding component with a molecular weight of 60 kD. The aim of our study was to analyze the biological functions of the 60-kD component. Sera of patients with AD were fractionated by ammoniumsulfate precipitation, gel filtration, affinity chromatography on IgE-Sepharose or anti-CD23 Sepharose and electroelution from SDS/PAGE. The sCD23-containing preparations were used in cell culture experiments to stimulate peripheral blood lymphocytes of normal donors. Binding studies with IgE peptides demonstrated that CD23 and the 60-kD IgE-binding components bind to the same site. Further experiments were performed to analyze the induced mRNA pattern in the presence of the 60-kD components by polymerase chain reaction (PCR). These data demonstrated that signals for IgE-germ line transcripts and IFN-γ were induced in the presence of the IgE-binding factor preparations from normal peripheral blood lymphocytes whereas there was no signal obtained for IL-2 or IL-4. In addition, it was shown by flow cytometry that the 60-kD component enhanced the expression of adhesion molecules (CD11α, CD18, CD54) whereas the expression of CD23 was reduced.

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http://dx.doi.org/10.1159/000236289DOI Listing

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