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研究食物过敏的实验模型。

Experimental Models for Studying Food Allergy.

机构信息

Division of Gastroenterology, Hepatology and Nutrition, Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.

出版信息

Cell Mol Gastroenterol Hepatol. 2018 Jun 7;6(3):356-369.e1. doi: 10.1016/j.jcmgh.2018.05.010. eCollection 2018.

DOI:10.1016/j.jcmgh.2018.05.010
PMID:30182049
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6121159/
Abstract

Immunoglobulin E-mediated food allergy is rapidly developing into a global health problem. Publicly available therapeutic intervention strategies are currently restricted to allergen avoidance and emergency treatments. To gain a better understanding of the disease pathophysiology so that new therapies can be developed, major research efforts have been put into studying food allergy in mice. Animal models should reflect the human pathology as closely as possible to allow for a rapid translation of basic science observations to the bedside. In this regard, experimental models of food allergy provide significant challenges for research because of discrepancies between the presentation of disease in humans and mice. The goal of this review is to give a summary of commonly used murine disease models and to discuss how they relate to the human condition. We will focus on epicutaneous sensitization models, on mouse strains that sensitize spontaneously to food as seen in humans, and on models in humanized animals. In summary, expanding the research toolbox of experimental food allergy provides an important step toward closing gaps in our understanding of the derailing immune mechanism that underlies the human disease. The availability of additional experimental models will provide exciting opportunities to discover new intervention points for the treatment of food allergies. .

摘要

免疫球蛋白 E 介导的食物过敏正在迅速成为一个全球性的健康问题。目前,公众可获得的治疗干预策略仅限于过敏原回避和紧急治疗。为了更好地了解疾病的病理生理学,从而开发新的治疗方法,人们投入了大量的研究努力来研究小鼠的食物过敏。动物模型应尽可能密切地反映人类的病理生理学,以便能够迅速将基础科学观察转化为临床实践。在这方面,由于人类和小鼠疾病表现的差异,食物过敏的实验模型为研究带来了重大挑战。本文的目的是总结常用的小鼠疾病模型,并讨论它们与人类疾病的关系。我们将重点介绍经皮致敏模型、与人一样会自发致敏食物的小鼠品系,以及人源化动物模型。总之,扩大实验性食物过敏的研究工具包是朝着缩小我们对人类疾病背后失控免疫机制的理解差距迈出的重要一步。更多实验模型的出现将为发现治疗食物过敏的新干预点提供令人兴奋的机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f659/6121159/60b59513d1c7/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f659/6121159/60b59513d1c7/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f659/6121159/60b59513d1c7/fx1.jpg

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本文引用的文献

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Maternal IgG immune complexes induce food allergen-specific tolerance in offspring.母体 IgG 免疫复合物可诱导子代对食物过敏原产生特异性耐受。
J Exp Med. 2018 Jan 2;215(1):91-113. doi: 10.1084/jem.20171163. Epub 2017 Nov 20.
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Effect of Varying Doses of Epicutaneous Immunotherapy vs Placebo on Reaction to Peanut Protein Exposure Among Patients With Peanut Sensitivity: A Randomized Clinical Trial.不同剂量表皮免疫疗法与安慰剂对花生敏感患者花生蛋白暴露反应的影响:一项随机临床试验。
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Therapeutic and continuative effects of human umbilical cord-derived mesenchymal stromal cells in food-allergic mice.人脐带间充质基质细胞对食物过敏小鼠的治疗及持续作用
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Experimental models of antibiotic exposure and atopic disease.抗生素暴露与过敏性疾病的实验模型。
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Enhanced Effect of -Lactoglobulin Immunization in Mice with Mild Intestinal Deterioration Caused by Low-Dose Dextran Sulphate Sodium: A New Experimental Approach to Allergy Studies.低剂量葡聚糖硫酸钠致轻度肠道损伤小鼠中 - 乳球蛋白免疫的增强作用:一种新的过敏研究实验方法。
Nutrients. 2024 Oct 10;16(20):3430. doi: 10.3390/nu16203430.
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J Allergy Clin Immunol. 2024 Sep;154(3):511-522. doi: 10.1016/j.jaci.2024.06.017. Epub 2024 Jul 5.
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Transglutaminase-Cross-Linked Tofu Suppressed Soybean-Induced Allergic Reactions by Enhancing Intestinal Mucosa Immune Tolerance.转谷氨酰胺酶交联豆腐通过增强肠道黏膜免疫耐受性抑制大豆诱导的过敏反应。
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表皮屏障破坏通过 IL-33 在小鼠中诱导调节性 T 细胞。
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J Clin Invest. 2016 Oct 3;126(10):4030-4044. doi: 10.1172/JCI85129. Epub 2016 Sep 19.
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IL-23 induced in keratinocytes by endogenous TLR4 ligands polarizes dendritic cells to drive IL-22 responses to skin immunization.内源性Toll样受体4配体在角质形成细胞中诱导产生的白细胞介素-23使树突状细胞极化,从而驱动白细胞介素-22对皮肤免疫的应答。
J Exp Med. 2016 Sep 19;213(10):2147-66. doi: 10.1084/jem.20150376. Epub 2016 Aug 22.