INHIBITION OF AN IN-VIVO ANTIGEN-SPECIFIC IGE RESPONSE BY ANTIBODIES TO CD23

被引:113
作者
FLORESROMO, L
SHIELDS, J
HUMBERT, Y
GRABER, P
AUBRY, JP
GAUCHAT, JF
AYALA, G
ALLET, B
CHAVEZ, M
BAZIN, H
CAPRON, M
BONNEFOY, JY
机构
[1] GLAXO INST MOLEC BIOL,CP 674,CH-1228 GENEVA,SWITZERLAND
[2] UNIV CATHOLIQUE LOUVAIN,FAC MED,EXPTL IMMUNOL UNIT,B-1200 BRUSSELS,BELGIUM
[3] CTR IMMUNOL & BIOL PARASITAIRE,CNRS 624,INSERM,U167,F-59019 LILLE,FRANCE
关键词
D O I
10.1126/science.8351517
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Immunoglobulin E (IgE) mediates many allergic responses. CD23 is a 45-kilodalton type II transmembrane glycoprotein expressed in many cell types. It is a low-affinity IgE receptor and interacts specifically with CD21, thereby modulating IgE production by B lymphocytes in vitro. In an in vivo model of an allergen-specific IgE response, administration of a rabbit polyclonal antibody to recombinant human truncated CD23 resulted in up to 90 percent inhibition of ovalbumin-specific IgE synthesis. Both Fabs and intact IgG inhibited IgE production in vitro and in vivo. Thus, CD23 participates in the regulation of IgE synthesis in vivo and so could be important in allergic disease.
引用
收藏
页码:1038 / 1041
页数:4
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