EOSINOPHIL IGE RECEPTOR AND CD23

被引:18
作者
CAPRON, M
TRUONG, MJ
ALDEBERT, D
GRUART, V
SUEMURA, M
DELESPESSE, G
TOURVIEILLE, B
CAPRON, A
机构
[1] OSAKA UNIV HOSP, DEPT INTERNAL MED, OSAKA, JAPAN
[2] HOP NOTRE DAME DE BON SECOURS, CTR RECH ALLERGIE, MONTREAL H2L 4K8, QUEBEC, CANADA
关键词
EOSINOPHILS; FC RECEPTORS FOR IGE; CD23; FLOW CYTOMETRY; NORTHERN BLOT; CYTOTOXICITY; IGE BINDING;
D O I
10.1007/BF02919131
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In the present review, eosinophil FcepsilonRII 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, an anti-eosinophil FcepsilonRII. 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.
引用
收藏
页码:252 / 259
页数:8
相关论文
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