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本文引用的文献

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[Cytokines in the pathogeny of celiac disease].[细胞因子在乳糜泻发病机制中的作用]
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2
New IL-12-family members: IL-23 and IL-27, cytokines with divergent functions.新型白细胞介素-12家族成员:白细胞介素-23和白细胞介素-27,功能各异的细胞因子。
Nat Rev Immunol. 2005 Jul;5(7):521-31. doi: 10.1038/nri1648.
3
Commentary: the role of the IL-18 system and other members of the IL-1R/TLR superfamily in innate mucosal immunity and the pathogenesis of inflammatory bowel disease: friend or foe?述评:白细胞介素-18系统及白细胞介素-1受体/Toll样受体超家族其他成员在先天性黏膜免疫及炎症性肠病发病机制中的作用:是友还是敌?
Eur J Immunol. 2004 Sep;34(9):2347-55. doi: 10.1002/eji.200425351.
4
Interleukin 15: a key to disrupted intraepithelial lymphocyte homeostasis and lymphomagenesis in celiac disease.白细胞介素15:乳糜泻中上皮内淋巴细胞稳态破坏和淋巴瘤发生的关键因素。
Gastroenterology. 2003 Sep;125(3):730-45. doi: 10.1016/s0016-5085(03)01047-3.
5
Paradoxical coexpression of proinflammatory and down-regulatory cytokines in intestinal T cells in childhood celiac disease.儿童乳糜泻肠道T细胞中促炎细胞因子和下调调节细胞因子的矛盾共表达。
Gastroenterology. 2002 Sep;123(3):667-78. doi: 10.1053/gast.2002.35355.
6
Inflammatory cytokines in small intestinal mucosa of patients with potential coeliac disease.潜在性腹腔疾病患者小肠黏膜中的炎性细胞因子
Clin Exp Immunol. 2002 Apr;128(1):94-101. doi: 10.1046/j.1365-2249.2002.01798.x.
7
Interleukin 18 and associated markers of T helper cell type 1 activity in coeliac disease.乳糜泻中白细胞介素18及辅助性T细胞1型活性的相关标志物
Gut. 2002 Feb;50(2):186-90. doi: 10.1136/gut.50.2.186.
8
When is a coeliac a coeliac? Report of a working group of the United European Gastroenterology Week in Amsterdam, 2001.乳糜泻患者何时被确诊为乳糜泻?2001年阿姆斯特丹欧洲胃肠病学周一个工作组的报告。
Eur J Gastroenterol Hepatol. 2001 Sep;13(9):1123-8. doi: 10.1097/00042737-200109000-00023.
9
Keratinocyte growth factor and coeliac disease.角质形成细胞生长因子与乳糜泻
Gut. 2001 Aug;49(2):176-81. doi: 10.1136/gut.49.2.176.
10
Role of interferon alpha in promoting T helper cell type 1 responses in the small intestine in coeliac disease.干扰素α在乳糜泻患者小肠中促进1型辅助性T细胞应答的作用。
Gut. 2001 Mar;48(3):425-9. doi: 10.1136/gut.48.3.425.

白细胞介素18维持乳糜泻患者的长期炎症。

Interleukin 18 maintains a long-standing inflammation in coeliac disease patients.

作者信息

León A J, Garrote J A, Blanco-Quirós A, Calvo C, Fernández-Salazar L, Del Villar A, Barrera A, Arranz E

机构信息

Department of Paediatrics and Immunology, and Institute of Biology and Molecular Genetics (IBGM), Universidad de Valladolid, Valladolid, Spain.

出版信息

Clin Exp Immunol. 2006 Dec;146(3):479-85. doi: 10.1111/j.1365-2249.2006.03239.x.

DOI:10.1111/j.1365-2249.2006.03239.x
PMID:17100768
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1810422/
Abstract

Dietary gluten induces an early response in the intestine of coeliac disease patients (CD), within a few hours, and this is driven by high levels of proinflammatory cytokines, including IFNgamma and IL-15, as has been thoroughly shown by gluten stimulation of biopsy explants. Our aim was to identify the immune mediators involved in the long-standing inflammation in untreated CD patients at diagnosis. mRNA and protein levels of TNFalpha, IL-12(p35), IL-12(p40), IL-15, IL-18 and IL-23(p19) were quantified in biopsies from active CD patients, CD patients on a gluten-free diet (GFD), healthy controls, and patients with non-CD inflammation and mild histological changes in the intestine. Biopsies from CD patients on a GFD were also stimulated in vitro with gliadin, and protein expression of IL-15 and IL-18 was analysed. Levels of IL-12 and IL-23 mRNA are nearly absent, and TNFalpha levels remain unchanged among different groups. Both the active and inactive forms of IL-18 protein have been found in all samples from active CD, and protein expression was only localized within the crypts. Levels of IL-15 mRNA remain unchanged, and protein expression, localized within the lamina propria, is found in a small number of samples. In vitro stimulation with gluten induces the expression of IL-15 and IL-18. In active CD, the early response following gluten intake characterized by high IFNgamma levels is driven by IL-18, and probably IL-15, and this alternates with periods of long-standing inflammation with moderate IFNgamma levels, maintained by IL-18 alone.

摘要

膳食中的麸质会在数小时内引发乳糜泻(CD)患者肠道的早期反应,这是由高水平的促炎细胞因子驱动的,包括干扰素γ(IFNγ)和白细胞介素15(IL-15),麸质对活检外植体的刺激已充分证明了这一点。我们的目的是确定未经治疗的CD患者在诊断时长期炎症中涉及的免疫介质。对活动期CD患者、采用无麸质饮食(GFD)的CD患者、健康对照以及患有非CD炎症且肠道组织学变化轻微的患者的活检样本中肿瘤坏死因子α(TNFα)、白细胞介素12(p35)、白细胞介素12(p40)、白细胞介素15、白细胞介素18和白细胞介素23(p19)的mRNA和蛋白质水平进行了定量分析。还对采用GFD的CD患者的活检样本进行了麦醇溶蛋白的体外刺激,并分析了白细胞介素15和白细胞介素18的蛋白质表达。白细胞介素12和白细胞介素23的mRNA水平在不同组中几乎不存在,TNFα水平保持不变。在活动期CD的所有样本中均发现了白细胞介素18蛋白的活性和非活性形式,且蛋白质表达仅局限于隐窝内。白细胞介素1