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通过体内成像系统早期检测T细胞转移诱导的自身免疫性结肠炎

Early Detection of T cell Transfer-induced Autoimmune Colitis by In Vivo Imaging System.

作者信息

Chen Yu-Ling, Chen Yi-Ting, Lo Cheng-Feng, Hsieh Ching-I, Chiu Shang-Yi, Wu Chang-Yen, Yeh Yu-Shan, Hung Shu-Hsuan, Cheng Po-Hao, Su Yu-Hsuan, Jiang Si-Tse, Chin Hsian-Jean, Su Yu-Chia

机构信息

National Laboratory Animal Center, National Applied Research Laboratories, Taipei, Taiwan.

Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan.

出版信息

Sci Rep. 2016 Oct 20;6:35635. doi: 10.1038/srep35635.

DOI:10.1038/srep35635
PMID:27762297
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5071899/
Abstract

Inflammatory bowel disease is a chronic and progressive inflammatory intestinal disease that includes two major types, namely ulcerative colitis and Crohn's disease (CD). CD is characterized by intestinal epithelial hyperplasia and inflammatory cell infiltration. Transfer of CD25CD45RBCD4 (naïve) T cells into immunodeficiency mice induces autoimmune colitis with pathological lesions similar to CD and loss of body weight 4 weeks after cell transfer. However, weight loss neither has sufficient sensitivity nor totally matches the pathological findings of CD. To establish an early and sensitive indicator of autoimmune colitis model, the transferred T cell-induced colitis mouse model was modified by transferring luciferase-expressing donor T cells and determining the colitis by in vivo imaging system (IVIS). Colitis was detected with IVIS 7-10 days before the onset of body weight loss and diarrhea. IVIS was also applied in the dexamethasone treatment trial, and was a more sensitive indicator than body weight changes. All IVIS signals were parallel to the pathological abnormalities of the gut and immunological analysis results. In summary, IVIS provides both sensitive and objective means to monitor the disease course of transferred T cell-induced CD and fulfills the 3Rs principle of humane care of laboratory animals.

摘要

炎症性肠病是一种慢性进行性肠道炎症性疾病,包括两种主要类型,即溃疡性结肠炎和克罗恩病(CD)。CD的特征是肠道上皮增生和炎症细胞浸润。将CD25CD45RBCD4(幼稚)T细胞转移到免疫缺陷小鼠中,可诱导出与CD相似的具有病理损伤的自身免疫性结肠炎,且在细胞转移后4周体重减轻。然而,体重减轻既没有足够的敏感性,也不完全与CD的病理结果相符。为了建立自身免疫性结肠炎模型的早期敏感指标,通过转移表达荧光素酶的供体T细胞并利用体内成像系统(IVIS)确定结肠炎,对转移T细胞诱导的结肠炎小鼠模型进行了改良。在体重减轻和腹泻发作前7 - 10天,通过IVIS检测到结肠炎。IVIS还应用于地塞米松治疗试验,并且是比体重变化更敏感的指标。所有IVIS信号均与肠道的病理异常和免疫学分析结果平行。总之,IVIS为监测转移T细胞诱导的CD的病程提供了敏感且客观的手段,并符合实验动物人道护理的3R原则。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8221/5071899/9ed1ab09c4fe/srep35635-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8221/5071899/aa33460f4d3a/srep35635-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8221/5071899/4dc082da191c/srep35635-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8221/5071899/3dfa259687a7/srep35635-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8221/5071899/4e53b8eacd4c/srep35635-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8221/5071899/a8b6b1587591/srep35635-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8221/5071899/9ed1ab09c4fe/srep35635-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8221/5071899/aa33460f4d3a/srep35635-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8221/5071899/4dc082da191c/srep35635-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8221/5071899/3dfa259687a7/srep35635-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8221/5071899/4e53b8eacd4c/srep35635-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8221/5071899/a8b6b1587591/srep35635-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8221/5071899/9ed1ab09c4fe/srep35635-f6.jpg

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Mediators Inflamm. 2015;2015:816460. doi: 10.1155/2015/816460. Epub 2015 May 18.
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Induction of Murine Intestinal Inflammation by Adoptive Transfer of Effector CD4+ CD45RB high T Cells into Immunodeficient Mice.通过将效应性CD4+ CD45RB高表达T细胞过继转移至免疫缺陷小鼠诱导小鼠肠道炎症。
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