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在致命性过敏反应小鼠模型中使用负载花生蛋白的聚合物纳米颗粒进行口服免疫疗法。

Oral immunotherapy using polymeric nanoparticles loaded with peanut proteins in a murine model of fatal anaphylaxis.

作者信息

Gamazo Carlos, García-Azpíroz Maddi, Souza Rebouças Juliana De, Gastaminza Gabriel, Ferrer Marta, Irache Juan M

机构信息

Department of Microbiology, University of Navarra, Instituto de Investigación Sanitaria de Navarra (Idisna), C/Irunlarrea, 1; 31080 - Pamplona, Spain.

Laboratory of Microbiology & Immunoregulation, Gonçalo Moniz Institute, Oswaldo Cruz Foundation (FIOCRUZ), Salvador, Brazil.

出版信息

Immunotherapy. 2017 Nov;9(15):1205-1217. doi: 10.2217/imt-2017-0111.

Abstract

BACKGROUND

Peanut allergy is the most common cause of anaphylaxis and food-related death. However, there is currently no approved immunotherapy treatment. Hence, this warrants the need for relevant and convenient animal models to test for adequate immunotherapies.

MATERIALS & METHODS: In this study, we compared three mouse strains: CD1, BALB/c and C57, to select a model of peanut allergy. After that, we conducted then a therapeutic study using an immunogenic peanut extract encapsulated in nanoparticles made with polymer Gantrez following the solvent displacement method.

RESULTS & CONCLUSION: After implementing a dosing schedule with oral commercial peanut butter, the antibody responses, cytokine profiles and, above all, the anaphylaxis induced after a challenge with peanut proteins, showed that the outbred CD1 strain was the most susceptible to peanut sensitization. CD1 sensitized mice were orally immunized with three doses of the nanoparticle formulation capable of protecting them against the severe anaphylactic symptoms induced by the peanut challenge.

摘要

背景

花生过敏是过敏反应和食物相关死亡的最常见原因。然而,目前尚无获批的免疫疗法。因此,这就需要相关且便捷的动物模型来测试合适的免疫疗法。

材料与方法

在本研究中,我们比较了三种小鼠品系:CD1、BALB/c和C57,以选择花生过敏模型。之后,我们采用溶剂置换法,使用包裹在由聚合物甘胆酸制成的纳米颗粒中的免疫原性花生提取物进行了一项治疗研究。

结果与结论

在用市售花生酱实施给药方案后,抗体反应、细胞因子谱,最重要的是,在用花生蛋白激发后诱导的过敏反应表明,远交系CD1品系对花生致敏最敏感。用三剂纳米颗粒制剂对CD1致敏小鼠进行口服免疫,可保护它们免受花生激发诱导的严重过敏症状。

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