
doi: 10.1007/bf02919131
pmid: 1287119
In the present review, eosinophil Fc epsilon RII was compared to CD23, a differentiation marker of B cells. Biochemical analysis revealed that molecules of similar molecular weight were immunoprecipitated from eosinophils and B cells by an anti-CD23 monoclonal antibody (mAb) or by BB10, and anti-eosinophil Fc epsilon RII. By flow cytometry, a correlation was found between the binding of anti-CD23 mAb and myeloma IgE. However, a low expression of different epitopes of CD23 was observed in various hypereosinophilic patients. Northern blot analysis of eosinophil RNA with the cDNA probe of CD23 revealed a weak message in only 3 of the 6 patients expressing membrane CD23. The inhibition by anti-CD23 mAbs of IgE-mediated cytotoxicity and IgE binding to eosinophils clearly indicated the participation of CD23 or a related molecule in IgE-dependent eosinophil functions. However, the differential effects of anti-CD23 mAbs on eosinophils and B cells suggest major differences in the characteristics of the molecule expressed by eosinophils and by B cells.
Cytotoxicity, Immunologic, Receptors, IgE, Cytotoxicity, Antibodies, Monoclonal, Northern blot, Flow Cytometry, [SDV] Life Sciences [q-bio], Eosinophils, Humans, Flow cytometry, CD23, Fc receptors for IgE, RNA, Messenger, IgE binding
Cytotoxicity, Immunologic, Receptors, IgE, Cytotoxicity, Antibodies, Monoclonal, Northern blot, Flow Cytometry, [SDV] Life Sciences [q-bio], Eosinophils, Humans, Flow cytometry, CD23, Fc receptors for IgE, RNA, Messenger, IgE binding
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