Co-receptors of B lymphocytes

被引:59
作者
ORourke, L
Tooze, R
Fearon, DT
机构
[1] Wellcome Trust Immunology Unit, Univ. Cambridge Sch. Clin. Med., C., Cambridge
基金
英国惠康基金;
关键词
D O I
10.1016/S0952-7915(97)80077-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The past year has seen advances in our understanding of accessory membrane proteins that modulate the B cell response to antigen-receptor stimulation. The generation of complement receptor deficient mice has reinforced our appreciation of the importance of complement receptors in the B cell response to antigen. The association of inositol polyphosphate B-phosphatase with Fc gamma RIIB suggests another mechanism; in addition to recruitment of the phosphotyrosine phosphatase SHP-1, by which secreted immunoglobulin can limit further response to antigen. The in vivo function of CD22 in regulating the threshold of antigen-receptor signalling has been shown using CD22-deficient mice. Lastly, B cell receptor signalling in the B-1 subset of B lymphocytes has been demonstrated to be negatively regulated by CD5.
引用
收藏
页码:324 / 329
页数:6
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