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Single-cell atlas of colonic CD8 T cells in ulcerative colitis.溃疡性结肠炎结肠 CD8 T 细胞单细胞图谱。
Nat Med. 2020 Sep;26(9):1480-1490. doi: 10.1038/s41591-020-1003-4. Epub 2020 Aug 3.
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Mitochondrial DNA in inflammation and immunity.线粒体 DNA 与炎症和免疫。
EMBO Rep. 2020 Apr 3;21(4):e49799. doi: 10.15252/embr.201949799. Epub 2020 Mar 23.
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Positioning Therapies in Ulcerative Colitis.溃疡性结肠炎的定位疗法
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Cytokine Networks in the Pathophysiology of Inflammatory Bowel Disease.细胞因子网络在炎症性肠病发病机制中的作用。
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Colonic epithelial cell diversity in health and inflammatory bowel disease.健康和炎症性肠病中的结肠上皮细胞多样性。
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Mitochondrial DNA Is a Pro-Inflammatory Damage-Associated Molecular Pattern Released During Active IBD.线粒体 DNA 是活动性 IBD 期间释放的促炎损伤相关分子模式。
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Risk of Serious and Opportunistic Infections Associated With Treatment of Inflammatory Bowel Diseases.炎症性肠病治疗相关的严重和机会性感染风险。
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Effect of tight control management on Crohn's disease (CALM): a multicentre, randomised, controlled phase 3 trial.紧密控制管理对克罗恩病(CALM)的影响:一项多中心、随机、对照的 3 期临床试验。
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MDR1 deficiency impairs mitochondrial homeostasis and promotes intestinal inflammation.MDR1 缺乏会损害线粒体动态平衡并促进肠道炎症。
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MARVEL试验:口服MitoQ治疗中度溃疡性结肠炎的2b期随机安慰剂对照试验。

The MARVEL trial: a phase 2b randomised placebo-controlled trial of oral MitoQ in moderate ulcerative colitis.

作者信息

Gwyer Findlay Emily, Sutton Greg, Ho Gwo-Tzer

机构信息

Centre for Inflammation Research, College of Medicine and Veterinary Medicine, University of Edinburgh, Edinburgh, UK.

Centre for Cardiovascular Science, College of Medicine and Veterinary Medicine, University of Edinburgh, Edinburgh, UK.

出版信息

Immunother Adv. 2020 Nov 12;1(1):ltaa002. doi: 10.1093/immadv/ltaa002. eCollection 2021 Jan.

DOI:10.1093/immadv/ltaa002
PMID:36284899
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9585668/
Abstract

Ulcerative colitis (UC) is an inflammatory disease of the large bowel which is characterised by dysregulated immunity and death to epithelial cells in the bowel, leading to prolonged inflammation. This can ultimately lead to surgery to remove the large bowel, with a risk of cancer developing if inflammation persists. Current therapies - which target the incoming immune cells or the cytokines they produce - are improving significantly but they are expensive and are immunosuppressive, leading to risk of infection. Here, we discuss a new trial which targets an early inducer of inflammation - the production of reactive oxygen species (ROS) by mitochondria. Previous work has shown that excessive mitochondrial ROS induces inflammatory signalling through the cGAS-STING pathway, leading to dysregulated immunity and death of epithelial cells. In this MARVEL trial (itochondrial nti-oxidant therapy to esol Inflammation in Ucerative Colitis) individuals with an active UC flare-up will be given a mitochondrial anti-oxidant (MitoQ) or placebo tablet in addition to standard medical treatment, in order to suppress inflammation as it develops. This phase 2b trial will repurpose MitoQ, which has been previously tested in other large trials in different disease settings, and will measure clinical response and markers of inflammation over 24 weeks. It is hoped that this trial will develop a new target for UC through re-purposing a relatively cheap, non-toxic and well-characterised drug.

摘要

溃疡性结肠炎(UC)是一种大肠的炎症性疾病,其特征是免疫失调以及肠道上皮细胞死亡,导致炎症持续存在。这最终可能导致切除大肠的手术,如果炎症持续存在,还会有患癌风险。目前的治疗方法——针对进入的免疫细胞或它们产生的细胞因子——正在显著改善,但它们价格昂贵且具有免疫抑制作用,会导致感染风险。在此,我们讨论一项新试验,该试验针对炎症的早期诱导因素——线粒体产生的活性氧(ROS)。先前的研究表明,过量的线粒体ROS通过cGAS-STING途径诱导炎症信号,导致免疫失调和上皮细胞死亡。在这项MARVEL试验(线粒体抗氧化疗法治疗溃疡性结肠炎中的炎症)中,除标准药物治疗外,患有活动性UC发作的个体将服用线粒体抗氧化剂(MitoQ)或安慰剂片剂,以便在炎症发生时进行抑制。这项2b期试验将重新利用MitoQ,它此前已在不同疾病背景下的其他大型试验中进行过测试,并将在24周内测量临床反应和炎症标志物。希望通过重新利用一种相对便宜、无毒且特性明确的药物,该试验能为UC开发出一个新的治疗靶点。