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J Immunol. 2013 Nov 1;191(9):4748-58. doi: 10.4049/jimmunol.1300122. Epub 2013 Sep 25.
2
The retinoic acid receptor agonist Am80 increases mucosal inflammation in an IL-6 dependent manner during Trichuris muris infection.视黄酸受体激动剂 Am80 在感染旋毛虫时以依赖于白细胞介素-6 的方式增加黏膜炎症。
J Clin Immunol. 2013 Nov;33(8):1386-94. doi: 10.1007/s10875-013-9936-8. Epub 2013 Sep 15.
3
Advances in pathogenesis and therapy of hemolytic uremic syndrome caused by Shiga toxin-2.产志贺样毒素 2 所致溶血尿毒综合征的发病机制和治疗进展。
IUBMB Life. 2013 Oct;65(10):827-35. doi: 10.1002/iub.1206. Epub 2013 Sep 6.
4
Immunization with a chimera consisting of the B subunit of Shiga toxin type 2 and brucella lumazine synthase confers total protection against Shiga toxins in mice.用志贺毒素 2 型的 B 亚单位和布鲁氏菌黄素合酶组成的嵌合体免疫小鼠可完全预防志贺毒素。
J Immunol. 2013 Sep 1;191(5):2403-11. doi: 10.4049/jimmunol.1300999. Epub 2013 Aug 5.
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The oxidative stress induced in vivo by Shiga toxin-2 contributes to the pathogenicity of haemolytic uraemic syndrome.体内由志贺毒素 2 引起的氧化应激有助于溶血性尿毒综合征的发病机制。
Clin Exp Immunol. 2013 Sep;173(3):463-72. doi: 10.1111/cei.12124.
6
Functional capacity of Shiga-toxin promoter sequences in eukaryotic cells.真核细胞中志贺毒素启动子序列的功能能力。
PLoS One. 2013;8(2):e57128. doi: 10.1371/journal.pone.0057128. Epub 2013 Feb 22.
7
Ethanolamine controls expression of genes encoding components involved in interkingdom signaling and virulence in enterohemorrhagic Escherichia coli O157:H7.乙醇胺控制肠出血性大肠杆菌 O157:H7 中涉及种间信号和毒力的基因编码组件的表达。
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Vitamin A supplements for preventing mortality, illness, and blindness in children aged under 5: systematic review and meta-analysis.维生素 A 补充剂预防 5 岁以下儿童死亡、疾病和失明:系统评价和荟萃分析。
BMJ. 2011 Aug 25;343:d5094. doi: 10.1136/bmj.d5094.
9
Mouse models of Escherichia coli O157:H7 infection and shiga toxin injection.大肠杆菌O157:H7感染和志贺毒素注射的小鼠模型。
J Biomed Biotechnol. 2011;2011:258185. doi: 10.1155/2011/258185. Epub 2011 Jan 3.
10
Vitamin A supplementation modifies the association between mucosal innate and adaptive immune responses and resolution of enteric pathogen infections.维生素 A 补充剂可改变黏膜固有和适应性免疫反应与肠道病原体感染消退之间的关系。
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视黄醇水平影响肠出血性大肠杆菌感染和小鼠对志贺毒素 2 的易感性。

Retinoid levels influence enterohemorrhagic Escherichia coli infection and Shiga toxin 2 susceptibility in mice.

机构信息

Laboratorio de Patogénesis e Inmunología de Procesos Infecciosos, Instituto de Medicina Experimental (IMEX) (CONICET), Academia Nacional de Medicina, Buenos Aires, Argentina.

Servicio de Fisiopatogenia, Instituto Nacional de Enfermedades Infecciosas-ANLIS Dr. Carlos Malbrán, Buenos Aires, Argentina.

出版信息

Infect Immun. 2014 Sep;82(9):3948-57. doi: 10.1128/IAI.02191-14. Epub 2014 Jul 7.

DOI:10.1128/IAI.02191-14
PMID:25001607
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4187814/
Abstract

Enterohemorrhagic Escherichia coli (EHEC) is a food-borne pathogen that produces Shiga toxin (Stx) and causes hemorrhagic colitis. Under some circumstances, Stx produced within the intestinal tract enters the bloodstream, leading to systemic complications that may cause the potentially fatal hemolytic-uremic syndrome. Although retinoids like vitamin A (VA) and retinoic acid (RA) are beneficial to gut integrity and the immune system, the effect of VA supplementation on gastrointestinal infections of different etiologies has been controversial. Thus, the aim of this work was to study the influence of different VA status on the outcome of an EHEC intestinal infection in mice. We report that VA deficiency worsened the intestinal damage during EHEC infection but simultaneously improved survival. Since death is associated mainly with Stx toxicity, Stx was intravenously inoculated to analyze whether retinoid levels affect Stx susceptibility. Interestingly, while VA-deficient (VA-D) mice were resistant to a lethal dose of Stx2, RA-supplemented mice were more susceptible to it. Given that peripheral blood polymorphonuclear cells (PMNs) are known to potentiate Stx2 toxicity, we studied the influence of retinoid levels on the absolute number and function of PMNs. We found that VA-D mice had decreased PMN numbers and a diminished capacity to produce reactive oxygen species, while RA supplementation had the opposite effect. These results are in line with the well-known function of retinoids in maintaining the homeostasis of the gut but support the idea that they have a proinflammatory effect by acting, in part, on the PMN population.

摘要

产肠毒性大肠杆菌(EHEC)是一种食源性病原体,可产生志贺毒素(Stx)并引起出血性结肠炎。在某些情况下,肠道内产生的 Stx 进入血液,导致可能致命的溶血性尿毒综合征等全身性并发症。尽管类视黄醇(如维生素 A(VA)和维甲酸(RA))有益于肠道完整性和免疫系统,但 VA 补充对不同病因的胃肠道感染的影响一直存在争议。因此,本研究旨在研究不同 VA 状态对小鼠 EHEC 肠道感染结局的影响。我们报告称,VA 缺乏症使 EHEC 感染期间的肠道损伤恶化,但同时提高了生存率。由于死亡主要与 Stx 毒性有关,因此我们静脉接种了 Stx 以分析视黄醇水平是否影响 Stx 敏感性。有趣的是,尽管 VA 缺乏症(VA-D)小鼠对致死剂量的 Stx2 具有抗性,但补充 RA 的小鼠对其更敏感。鉴于已知外周血多形核粒细胞(PMN)可增强 Stx2 毒性,我们研究了视黄醇水平对 PMN 绝对数量和功能的影响。我们发现,VA-D 小鼠的 PMN 数量减少,产生活性氧的能力降低,而 RA 补充则具有相反的作用。这些结果与视黄醇在维持肠道内稳态方面的已知功能一致,但支持这样一种观点,即它们通过部分作用于 PMN 群体而具有促炎作用。