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一种用于花生过敏的新生猪模型。

A neonatal swine model for peanut allergy.

作者信息

Helm Ricki M, Furuta Glenn T, Stanley J Steve, Ye Jianhui, Cockrell Gael, Connaughton Cathie, Simpson Pippa, Bannon Gary A, Burks A Wesley

机构信息

Division of Allergy/Immunology, Department of Pediatrics, Arkansas Children's Hospital Research Institute, University of Arkansas for Medical Sciences, Little Rock 72201, USA.

出版信息

J Allergy Clin Immunol. 2002 Jan;109(1):136-42. doi: 10.1067/mai.2002.120551.

Abstract

BACKGROUND

Peanut allergy represents a significant health threat in the United States. The factors contributing to the severity of the allergic response and the immunopathogenic mechanisms underlying peanut allergy remain to be completely characterized. As yet, no animal model has been developed that will completely mimic the physical, immunologic, and histologic features of food allergy.

OBJECTIVE

The purpose of this investigation was to develop a neonatal pig model of peanut allergy that would mimic the allergic symptoms and the immunologic and histologic profile of human peanut allergy.

METHODS

Newborn piglets sensitized intraperitoneally with peanut extract and cholera toxin were orally challenged repeatedly with peanut meal. Physical symptoms, including emesis, lethargy, diarrhea, and respiratory distress, were monitored to determine the allergic response. Immunologic assessment was conducted through use of skin testing and the antigenic response to peanut proteins. Histologically, tissues derived from the esophagus, stomach, small intestine, and colon were assessed for morphologic changes after the oral challenge.

RESULTS

Peanut-sensitized pigs responded with physical symptoms that mimicked those seen in double-blinded, placebo-controlled oral food challenges to peanuts in children and adults. Skin testing suggested an IgE-mediated response; this was confirmed by a negative passive cutaneous anaphylaxis response of heat-treated sera obtained from peanut-sensitized animals. Damage to villi of the small intestine was similar to that seen in endoscopically obtained tissue specimens from certain food-allergic individuals.

CONCLUSION

The neonatal pig model of peanut allergy mimics the physical and immunologic characteristics of peanut allergy in human beings. The model will be useful for determining IgE-mediated mechanisms and conducting endoscopic histologic assessment of tissues and immunotherapeutic intervention strategies with repeated allergen challenges.

摘要

背景

花生过敏在美国是一个重大的健康威胁。导致过敏反应严重程度的因素以及花生过敏潜在的免疫致病机制仍有待全面阐明。迄今为止,尚未开发出能完全模拟食物过敏的生理、免疫和组织学特征的动物模型。

目的

本研究的目的是建立一种花生过敏的新生猪模型,该模型能模拟人类花生过敏的过敏症状以及免疫和组织学特征。

方法

用花生提取物和霍乱毒素对新生仔猪进行腹腔致敏,然后用花生粕反复进行口服激发。监测包括呕吐、嗜睡、腹泻和呼吸窘迫在内的生理症状,以确定过敏反应。通过皮肤试验和对花生蛋白的抗原反应进行免疫评估。在组织学上,评估口服激发后取自食管、胃、小肠和结肠的组织的形态学变化。

结果

花生致敏的猪出现的生理症状与儿童和成人在双盲、安慰剂对照的花生口服食物激发试验中观察到的症状相似。皮肤试验提示为IgE介导的反应;从花生致敏动物获得的热处理血清的阴性被动皮肤过敏反应证实了这一点。小肠绒毛的损伤与从某些食物过敏个体的内镜检查获得的组织标本中所见的损伤相似。

结论

花生过敏的新生猪模型模拟了人类花生过敏的生理和免疫特征。该模型将有助于确定IgE介导的机制,并对组织进行内镜组织学评估以及通过反复过敏原激发进行免疫治疗干预策略的研究。

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