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乳糜泻患者十二指肠上皮内Vα24不变自然杀伤T细胞增多。

Increased Intraepithelial Vα24 Invariant NKT Cells in the Celiac Duodenum.

作者信息

Montalvillo Enrique, Bernardo David, Martínez-Abad Beatriz, Allegretti Yessica, Fernández-Salazar Luis, Calvo Carmen, Chirdo Fernando G, Garrote José A, Arranz Eduardo

机构信息

Mucosal Immunology Lab, IBGM, University of Valladolid-CSIC, Sanz y Forés 3, 47003 Valladolid, Spain.

Antigen Presentation Research Group, Imperial College London, Northwick Park & St Mark's Campus, Level 7W, St Mark's Building Watford Road Harrow HA1 3UJ, UK.

出版信息

Nutrients. 2015 Oct 30;7(11):8960-76. doi: 10.3390/nu7115444.

DOI:10.3390/nu7115444
PMID:26529008
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4663572/
Abstract

Celiac Disease (CD) is an interferon (IFN)γ-mediated duodenal hypersensitivity to wheat gluten occurring in genetically predisposed individuals. Gluten-free diet (GFD) leads to a complete remission of the disease. Vα24-restricted invariant NKT (iNKT) cells are important to maintain immune homeostasis in the gut mucosa because of their unique capacity to rapidly produce large quantities of both T-helper (Th)1 and Th2 cytokines upon stimulation. We studied the presence of these cells in the CD duodenum. Duodenal biopsies were obtained from 45 untreated-CD patients (uCD), 15 Gluten Free Diet-CD patients (GFD-CD), 44 non-inflamed non-CD controls (C-controls) and 15 inflamed non-CD controls (I-controls). Two populations from Spain and Argentina were recruited. Messenger RNA (mRNA) expression of Vα24-Jα18 (invariant TCRα chain of human iNKT cells), IFNγ and intracellular transcription factor Forkhead Box P3 (Foxp3), and flow cytometry intraepithelial lymphocyte (IEL) profile were determined. Both uCD and GFD-CD patients had higher Vα24-Jα18 mRNA levels than non-CD controls (I and C-controls). The expression of Vα24-Jα18 correlated with Marsh score for the severity of mucosal lesion and also with increased mRNA IFNγ levels. uCD and GFD-CD patients had decreased mRNA expression of FoxP3 but increased expression of Vα24-Jα18, which revealed a CD-like molecular profile. Increased numbers of iNKT cells were confirmed by flow cytometry within the intraepithelial lymphocyte compartment of uCD and GFD-CD patients and correlated with Vα24-Jα18 mRNA expression. In conclusion, we have found an increased number of iNKT cells in the duodenum from both uCD and GFD-CD patients, irrespective of the mucosal status. A CD-like molecular profile, defined by an increased mRNA expression of Vα24-Jα18 together with a decreased expression of FoxP3, may represent a pro-inflammatory signature of the CD duodenum.

摘要

乳糜泻(CD)是一种由干扰素(IFN)γ介导的,发生于遗传易感性个体的十二指肠对小麦麸质的超敏反应。无麸质饮食(GFD)可使该病完全缓解。Vα24限制性不变自然杀伤T(iNKT)细胞对于维持肠道黏膜免疫稳态很重要,因为它们具有在受到刺激后迅速大量产生辅助性T(Th)1和Th2细胞因子的独特能力。我们研究了这些细胞在CD患者十二指肠中的存在情况。从45例未经治疗的CD患者(uCD)、15例接受无麸质饮食的CD患者(GFD-CD)、44例无炎症的非CD对照(C对照)和15例有炎症的非CD对照(I对照)中获取十二指肠活检组织。招募了来自西班牙和阿根廷的两个群体。测定了Vα24-Jα18(人类iNKT细胞的不变TCRα链)、IFNγ和细胞内转录因子叉头框P3(Foxp3)的信使核糖核酸(mRNA)表达,以及流式细胞术检测的上皮内淋巴细胞(IEL)谱。uCD和GFD-CD患者的Vα24-Jα18 mRNA水平均高于非CD对照(I和C对照)。Vα24-Jα18的表达与黏膜病变严重程度的马什评分相关,也与mRNA IFNγ水平升高相关。uCD和GFD-CD患者的FoxP3 mRNA表达降低,但Vα24-Jα18表达增加,这显示出类似CD的分子特征。通过流式细胞术证实,uCD和GFD-CD患者上皮内淋巴细胞区室中的iNKT细胞数量增加,且与Vα24-Jα18 mRNA表达相关。总之,我们发现uCD和GFD-CD患者十二指肠中的iNKT细胞数量均增加,与黏膜状态无关。由Vα24-Jα18 mRNA表达增加以及FoxP3表达降低所定义的类似CD的分子特征,可能代表了CD十二指肠的促炎特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2177/4663572/09bdffd83c2d/nutrients-07-05444-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2177/4663572/c54ad178fffc/nutrients-07-05444-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2177/4663572/09bdffd83c2d/nutrients-07-05444-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2177/4663572/c54ad178fffc/nutrients-07-05444-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2177/4663572/90472376dab0/nutrients-07-05444-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2177/4663572/754c31d5e0db/nutrients-07-05444-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2177/4663572/a8fbce0b0d98/nutrients-07-05444-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2177/4663572/e20bbf8eceb3/nutrients-07-05444-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2177/4663572/09bdffd83c2d/nutrients-07-05444-g006.jpg

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