Regulation of mast-cell and basophil function and survival by IgE

被引:481
作者
Kawakami, T
Galli, SJ
机构
[1] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Immunol & Microbiol, Stanford, CA 94305 USA
[3] La Jolla Inst Allergy & Immunol, Div Allergy, San Diego, CA 92121 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nri914
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mast cells and basophils are important effector cells in T helper 2 (T(H)2)-cell-dependent, immunoglobulin-E-associated allergic disorders and immune responses to parasites. The crosslinking of IgE that is bound to the high-affinity receptor Fcis an element ofRI with multivalent antigen results in the aggregation of Fcis an element ofRI and the secretion of products that can have effector, immunoregulatory or autocrine effects. This response can be enhanced markedly in cells that have been exposed to high levels of IgE, which results in the increased surface expression of Fcis an element ofRI. Moreover, recent work indicates that monomeric IgE (in the absence of crosslinking) can render mast cells resistant to apoptosis induced by growth-factor deprivation in vitro and, under certain circumstances, can induce the release of cytokines. So, the binding of IgE to Fcis an element ofRI might influence mast-cell and basophil survival directly or indirectly, and can also regulate cellular function.
引用
收藏
页码:773 / 786
页数:16
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