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经皮暴露于先前耐受的食物抗原诱导口腔过敏反应的小鼠模型。

Oral allergy induction through skin exposure to previously tolerated food antigens in murine models.

机构信息

Department of Pharmacology, Graduate School of Medicine, University of the Ryukyus, 207 Uehara, Nishihara, Okinawa, 903-0215, Japan.

Immuno-Pharmacology, Field of Biofunctional Control, Medical Information Science Division, United Graduate School of Drug Discovery and Medical Information Science, Gifu University, 1-1 Yanaido, Gifu 501-1194, Japan.

出版信息

J Pharmacol Sci. 2023 Jun;152(2):76-85. doi: 10.1016/j.jphs.2023.03.003. Epub 2023 Mar 30.

Abstract

Food allergies (FAs) are caused by a failure of the immune system to regulate oral tolerance (OT). The use of soap containing hydrolyzed wheat overrides acquired OT to wheat through skin exposure. However, in mouse models, the experimental OT is robust, suggesting that acquired OT to allergens prevents the development of FAs. We aimed to analyze the mechanisms and developed a mouse model of FA that overrides acquired OT via skin exposure. Three murine FA models (intraperitoneal [IP], epicutaneous [EC], and intradermal [ID]) were compared to evaluate if allergies to ovalbumin (OVA) that had been previously tolerated orally could be induced. In the ID model, OT was overridden, and allergic reactions of severe anaphylaxis were developed. To analyze this effect in the ID model, we measured the migration of dendritic cells (DCs) into lymph nodes. The induction of OT promoted the migration of CD103 dermal DCs; moreover, repeated percutaneous doses of OVA for sensitization gradually increased the migration of CD11b dermal DCs. The difference in the proportion of regulatory T cells between ID-sensitized groups at the first ID injection disappeared at the tenth injection. Although OT was robust in the IP model, ID sensitization was found to override OT.

摘要

食物过敏(FA)是由于免疫系统调节口服耐受(OT)失败引起的。使用含有水解小麦的肥皂通过皮肤暴露会破坏对小麦的获得性 OT。然而,在小鼠模型中,实验性 OT 是强大的,这表明对过敏原的获得性 OT 可防止 FA 的发展。我们旨在分析机制并开发一种通过皮肤暴露破坏获得性 OT 的 FA 小鼠模型。比较了三种小鼠 FA 模型(腹腔内[IP]、表皮[EC]和皮内[ID]),以评估先前经口耐受的卵清蛋白(OVA)是否可以诱导过敏。在 ID 模型中,OT 被破坏,并发展出严重过敏反应的过敏反应。为了分析 ID 模型中的这种作用,我们测量了树突状细胞(DC)向淋巴结的迁移。OT 的诱导促进了 CD103 真皮 DC 的迁移;此外,反复经皮给予 OVA 进行致敏逐渐增加了 CD11b 真皮 DC 的迁移。在第一次 ID 注射时,ID 致敏组之间调节性 T 细胞的比例差异在第十次注射时消失。尽管 IP 模型中的 OT 是强大的,但发现 ID 致敏可破坏 OT。

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