Tuning IgE: IgE-Associating Molecules and Their Effects on IgE-Dependent Mast Cell Reactions

被引:26
|
作者
Ando, Tomoaki [1 ]
Kitaura, Jiro [1 ,2 ]
机构
[1] Juntendo Univ, Grad Sch Med, Atopy Allergy Res Ctr, Tokyo 1138421, Japan
[2] Juntendo Univ, Grad Sch Med, Dept Sci Allergy & Inflammat, Tokyo 1138421, Japan
关键词
IgE; mast cells; basophils; FcERI; CD23; histamine-releasing factor (HRF); glycosylation; structure; omalizumab; FC-EPSILON-RI; HISTAMINE-RELEASING FACTOR; HIGH-AFFINITY RECEPTOR; CONTROLLED TUMOR PROTEIN; HUMAN-IMMUNOGLOBULIN-E; ACCELERATED DISSOCIATION; PROINFLAMMATORY ROLE; MONOCLONAL-ANTIBODY; CRYSTAL-STRUCTURE; GAMMA-RIIB;
D O I
10.3390/cells10071697
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The recent emergence of anti-immunoglobulin E (IgE) drugs and their candidates for humans has endorsed the significance of IgE-dependent pathways in allergic disorders. IgE is distributed locally in the tissues or systemically to confer a sensory mechanism in a domain of adaptive immunity to the otherwise innate type of effector cells, namely, mast cells and basophils. Bound on the high-affinity IgE receptor Fc epsilon RI, IgE enables fast memory responses against revisiting threats of venoms, parasites, and bacteria. However, the dysregulation of IgE-dependent reactions leads to potentially life-threatening allergic diseases, such as asthma and anaphylaxis. Therefore, reactivity of the IgE sensor is fine-tuned by various IgE-associating molecules. In this review, we discuss the mechanistic basis for how IgE-dependent mast cell activation is regulated by the IgE-associating molecules, including the newly developed therapeutic candidates.
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页数:18
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