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An immunoglobulin-like receptor, Allergin-1, inhibits immunoglobulin E–mediated immediate hypersensitivity reactions

机译:免疫球蛋白样受体Allergin-1抑制免疫球蛋白E介导的速发型超敏反应

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摘要

Anaphylaxis is a life-threatening immediate hypersensitivity reaction triggered by antigen capture by immunoglobulin E (IgE) bound to the high-affinity IgE receptor (FcεRI) on mast cells. However, the regulatory mechanism of mast cell activation is not completely understood. Here we identify an immunoglobulin-like receptor, Allergin-1, that contains an immunoreceptor tyrosine-based inhibitory motif (ITIM)-like domain, and show it was preferentially expressed on mast cells. Mouse Allergin-1 recruited the tyrosine phosphatases SHP-1 and SHP-2 and the inositol phosphatase SHIP. Coligation of Allergin-1 and FcεRI suppressed IgE-mediated degranulation of bone marrow–derived cultured mast cells. Moreover, mice deficient in Allergin-1 developed enhanced passive systemic and cutaneous anaphylaxis. Thus, Allergin-1 suppresses IgE-mediated, mast cell–dependent anaphylaxis in mice.
机译:过敏反应是威胁生命的立即超敏反应,由肥大细胞上与高亲和力IgE受体(FcεRI)结合的免疫球蛋白E(IgE)捕获抗原引发。但是,肥大细胞活化的调节机制尚不完全清楚。在这里,我们确定了一个免疫球蛋白样受体,Allergin-1,其中包含一个基于免疫受体酪氨酸的抑制性基序(ITIM)样域,并表明它优先在肥大细胞上表达。小鼠Allergin-1募集了酪氨酸磷酸酶SHP-1和SHP-2和肌醇磷酸酶SHIP。 Allergin-1和FcεRI的结合可抑制IgE介导的骨髓培养肥大细胞的脱颗粒。此外,缺乏Allergin-1的小鼠发展为被动的全身和皮肤过敏反应。因此,Allergin-1抑制小鼠中IgE介导的肥大细胞依赖性过敏反应。

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