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采用健康成人挑战模型对致腹泻性大肠埃希菌感染的病理生理决定因素进行特征分析。

Characterization of the pathophysiological determinants of diarrheagenic Escherichia coli infection using a challenge model in healthy adults.

机构信息

Department of Nutrition and Health, NIZO, PO Box 20, 6710 BA, Ede, the Netherlands.

Nestlé Institute of Health Sciences, Gastrointestinal Health, Nestlé Research, Lausanne, Switzerland.

出版信息

Sci Rep. 2021 Mar 15;11(1):6060. doi: 10.1038/s41598-021-85161-1.

Abstract

An experimental human challenge model with an attenuated diarrheagenic Escherichia coli (E. coli) strain has been used in food intervention studies aimed to increase resistance to E. coli infection. This study was designed to refine and expand this challenge model. In a double-blind study, healthy male subjects were orally challenged with 1E10 or 5E10 colony-forming units (CFU) of E. coli strain E1392/75-2A. Three weeks later, subjects were rechallenged with 1E10 CFU of E. coli. Before and after both challenges, clinical symptoms and infection- and immune-related biomarkers were analyzed. Subset analysis was performed on clinically high- and low-responders. Regardless of inoculation dose, the first challenge induced clinical symptoms for 2-3 days. In blood, neutrophils, CRP, CXCL10, and CFA/II-specific IgG were induced, and in feces calprotectin and CFA/II-specific IgA. Despite clinical differences between high- and low-responders, infection and immune biomarkers did not differ. The first inoculation induced protection at the second challenge, with a minor clinical response, and no change in biomarkers. The refined study design resulted in a larger dynamic range of symptoms, and identification of biomarkers induced by a challenge with the attenuated E. coli strain E1392/75-2A, which is of value for future intervention studies. Addition of a second inoculation allows to study the protective response induced by a primary infection.Clinicaltrials.gov registration: NCT02541695 (04/09/2015).

摘要

一个经改良的减毒腹泻性大肠杆菌(E. coli)感染的人体挑战模型已被用于食物干预研究,旨在增加对 E. coli 感染的抵抗力。本研究旨在对该挑战模型进行改进和扩展。在一项双盲研究中,健康男性志愿者经口接受 1E10 或 5E10 菌落形成单位(CFU)的 E. coli 菌株 E1392/75-2A 挑战。3 周后,志愿者用 1E10 CFU 的 E. coli 再次进行挑战。在两次挑战前后,分析临床症状和感染及免疫相关生物标志物。对临床高反应者和低反应者进行亚组分析。无论接种剂量如何,首次挑战均会引起 2-3 天的临床症状。在血液中,诱导中性粒细胞、CRP、CXCL10 和 CFA/II 特异性 IgG,在粪便中诱导钙卫蛋白和 CFA/II 特异性 IgA。尽管高反应者和低反应者之间存在临床差异,但感染和免疫生物标志物没有差异。首次接种在第二次接种时诱导了保护作用,仅有轻微的临床反应,且生物标志物无变化。改良后的研究设计导致症状的动态范围更大,并鉴定了经减毒 E. coli 菌株 E1392/75-2A 挑战诱导的生物标志物,这对未来的干预研究具有价值。添加第二次接种可研究初次感染诱导的保护反应。Clinicaltrials.gov 注册号:NCT02541695(2015 年 9 月 4 日)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c981/7960709/ee416c42f69a/41598_2021_85161_Fig1_HTML.jpg

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