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一种用于嗜酸性食管炎的新型猪生物医学研究模型的免疫学和病理学特征

Immunologic and pathologic characterization of a novel swine biomedical research model for eosinophilic esophagitis.

作者信息

Cortes Lizette M, Brodsky David, Chen Celine, Pridgen Tiffany, Odle Jack, Snider Douglas B, Cruse Glenn, Putikova Arina, Masuda Mia Y, Doyle Alfred D, Wright Benjamin L, Dawson Harry D, Blikslager Anthony, Dellon Evan S, Laster Scott M, Käser Tobias

机构信息

Department of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State University, Raleigh, NC, United States.

Center for Food Allergy Modeling in Pigs (CFAMP), Comparative Medicine Institute, North Carolina State University, Raleigh, NC, United States.

出版信息

Front Allergy. 2022 Nov 14;3:1029184. doi: 10.3389/falgy.2022.1029184. eCollection 2022.

Abstract

Eosinophilic esophagitis (EoE) is a chronic allergy-mediated condition with an increasing incidence in both children and adults. Despite EoE's strong impact on human health and welfare, there is a large unmet need for treatments with only one recently FDA-approved medication for EoE. The goal of this study was to establish swine as a relevant large animal model for translational biomedical research in EoE with the potential to facilitate development of therapeutics. We recently showed that after intraperitoneal sensitization and oral challenge with the food allergen hen egg white protein (HEWP), swine develop esophageal eosinophilia-a hallmark of human EoE. Herein, we used a similar sensitization and challenge treatment and evaluated immunological and pathological markers associated with human EoE. Our data demonstrate that the incorporated sensitization and challenge treatment induces (i) a systemic T-helper 2 and IgE response, (ii) a local expression of eotaxin-1 and other allergy-related immune markers, (iii) esophageal eosinophilia (>15 eosinophils/0.24 mm), and (iv) esophageal endoscopic findings including linear furrows and white exudates. Thereby, we demonstrate that our sensitization and oral challenge protocol not only induces the underlying immune markers but also the micro- and macro-pathological hallmarks of human EoE. This swine model for EoE represents a novel relevant large animal model that can drive translational biomedical research to develop urgently needed treatment strategies for EoE.

摘要

嗜酸性食管炎(EoE)是一种由慢性过敏介导的疾病,在儿童和成人中的发病率均呈上升趋势。尽管EoE对人类健康和福祉有重大影响,但目前仅有一种药物最近获得美国食品药品监督管理局(FDA)批准用于治疗EoE,治疗需求仍远未满足。本研究的目的是建立猪作为EoE转化生物医学研究的相关大型动物模型,以促进治疗方法的开发。我们最近发现,猪经腹腔致敏并口服食物过敏原蛋清蛋白(HEWP)后,会出现食管嗜酸性粒细胞增多,这是人类EoE的一个标志。在此,我们采用了类似的致敏和激发处理方法,并评估了与人类EoE相关的免疫和病理标志物。我们的数据表明,所采用的致敏和激发处理方法可诱导:(i)全身性辅助性T细胞2型和IgE反应;(ii)嗜酸性粒细胞趋化因子-1及其他过敏相关免疫标志物的局部表达;(iii)食管嗜酸性粒细胞增多(>15个嗜酸性粒细胞/0.24mm);以及(iv)食管内镜检查结果,包括线性沟纹和白色渗出物。因此,我们证明我们的致敏和口服激发方案不仅能诱导潜在的免疫标志物,还能诱导人类EoE的微观和宏观病理特征。这种EoE猪模型代表了一种新型的相关大型动物模型,可推动转化生物医学研究,以开发EoE急需的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/091b/9701751/bb4a161d185d/falgy-03-1029184-g001.jpg

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