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通过FcγRIII-组胺途径诱导具有独特皮肤表现的新型IgG过敏反应小鼠模型的建立。

Development of a Novel IgG Anaphylaxis Mouse Model with Uniquely Characteristic Skin Manifestations Induced Through the FcγRIII-Histamine Pathway.

作者信息

Terashi Masato, Yamaki Kouya, Koyama Yutaka

机构信息

Laboratory of Pharmacology, Kobe Pharmaceutical University, Kobe, Hyogo, Japan.

出版信息

Immunol Invest. 2023 Jan;52(1):83-103. doi: 10.1080/08820139.2022.2130799. Epub 2022 Oct 6.

Abstract

BACKGROUND

Studies of passive anaphylaxis, in which mouse immunoglobulin G (IgG) and its antigens are administered to mice, believe that platelet-activating factor (PAF) is more important than histamine and that basophils or macrophages are primarily involved. However, the full extent of IgG-dependent anaphylaxis is still unclear; that is, little agreement has been reached about the mechanism.

METHODS

First, we established the novel model of IgG anaphylaxis induced by the intravenous administration of two types of IgG and a fluorescent dye-labeled antigen, as IgG immune complex in HR-1 hairless mice. Subsequently, pharmacological analysis was used to investigate the underlying mechanisms of IgG anaphylaxis in this established model.

RESULTS

The novel IgG anaphylaxis model can induce the IgG-induced Anaphylaxis-dependent Spotted Distribution of fluorescently labeled Immune complexes in the Skin, named "G-ASDIS". Moreover, this model was triggered primarily by the FcγRIII-dependent histamine release, which is different from the conventional model in which PAF was involved in the development of IgG anaphylaxis. Basophils in the circulation and mast cells in the skin may participate in the development of IgG anaphylaxis and increased G-ASDIS.

CONCLUSION

Our results propose that the novel axis, namely the FcγRIII-basophils and/or mast cell-histamine pathway, is important for IgG anaphylaxis. Further analysis of our model in addition to other models will lead to a broader analysis and understanding of the IgG anaphylaxis mechanism.

摘要

背景

在被动过敏反应研究中,将小鼠免疫球蛋白G(IgG)及其抗原注射给小鼠,该研究认为血小板活化因子(PAF)比组胺更重要,且主要涉及嗜碱性粒细胞或巨噬细胞。然而,IgG依赖性过敏反应的全貌仍不清楚;也就是说,关于其机制尚未达成共识。

方法

首先,我们在HR-1无毛小鼠中建立了一种新型的IgG过敏反应模型,通过静脉注射两种类型的IgG和一种荧光染料标记的抗原作为IgG免疫复合物来诱导。随后,采用药理学分析来研究该建立模型中IgG过敏反应的潜在机制。

结果

这种新型的IgG过敏反应模型能够诱导IgG介导的皮肤中荧光标记免疫复合物的过敏反应依赖性斑点状分布,命名为“G-ASDIS”。此外,该模型主要由FcγRIII依赖性组胺释放触发,这与传统模型不同,传统模型中PAF参与了IgG过敏反应的发生。循环中的嗜碱性粒细胞和皮肤中的肥大细胞可能参与了IgG过敏反应的发生并增加了G-ASDIS。

结论

我们的结果表明,新的轴,即FcγRIII-嗜碱性粒细胞和/或肥大细胞-组胺途径,对IgG过敏反应很重要。除其他模型外,对我们模型的进一步分析将有助于更广泛地分析和理解IgG过敏反应机制。

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