• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

溃疡性结肠炎患者接受阿达木单抗治疗期间肠道微生物群组成的动态变化:对治疗反应预测和治疗靶点的意义

Dynamic changes in the gut microbiota composition during adalimumab therapy in patients with ulcerative colitis: implications for treatment response prediction and therapeutic targets.

作者信息

Oh Han Na, Shin Seung Yong, Kim Jong-Hwa, Baek Jihye, Kim Hyo Jong, Lee Kang-Moon, Park Soo Jung, Kim Seok-Young, Choi Hyung-Kyoon, Kim Wonyong, Sul Woo Jun, Choi Chang Hwan

机构信息

Department of Systems Biotechnology, Chung-Ang University, Anseong, 17546, Republic of Korea.

Inflamm-Aging Translational Research Center, Ajou University Medical Center, Suwon, Republic of Korea.

出版信息

Gut Pathog. 2024 Aug 26;16(1):44. doi: 10.1186/s13099-024-00637-5.

DOI:10.1186/s13099-024-00637-5
PMID:39187879
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11346184/
Abstract

BACKGROUND

While significant research exists on gut microbiota changes after anti-tumor necrosis factor-alpha (anti TNF-α) therapy for ulcerative colitis, little is known about the longitudinal changes related to the effects of anti TNF-α. This study aimed to investigate the dynamics of gut microbiome changes during anti TNF-α (adalimumab) therapy in patients with ulcerative colitis (UC).

RESULTS

The microbiota composition was affected by the disease severity and extent in patients with UC. Regardless of clinical remission status at each time point, patients with UC exhibited microbial community distinctions from healthy controls. Distinct amplicon sequence variants (ASVs) differences were identified throughout the course of Adalimumab (ADA) treatment at each time point. A notable reduction in gut microbiome dissimilarity was observed only in remitters. Remitters demonstrated a decrease in the relative abundances of Burkholderia-Caballeronia-Paraburkholderia and Staphylococcus as the treatment progressed. Additionally, there was an observed increase in the relative abundances of Bifidobacterium and Dorea. Given the distribution of the 48 ASVs with high or low relative abundances in the pre-treatment samples according to clinical remission at week 8, a clinical remission at week 8 with a sensitivity and specificity of 72.4% and 84.3%, respectively, was predicted on the receiver operating characteristic curve (area under the curve, 0.851).

CONCLUSIONS

The gut microbiota undergoes diverse changes according to the treatment response during ADA treatment. These changes provide insights into predicting treatment responses to ADA and offer new therapeutic targets for UC.

摘要

背景

虽然针对溃疡性结肠炎的抗肿瘤坏死因子-α(抗TNF-α)治疗后肠道微生物群变化已有大量研究,但对于与抗TNF-α作用相关的纵向变化知之甚少。本研究旨在调查溃疡性结肠炎(UC)患者在抗TNF-α(阿达木单抗)治疗期间肠道微生物组变化的动态情况。

结果

UC患者的微生物群组成受疾病严重程度和范围的影响。无论每个时间点的临床缓解状态如何,UC患者的微生物群落与健康对照存在差异。在阿达木单抗(ADA)治疗的每个时间点的整个过程中,都发现了明显的扩增子序列变体(ASV)差异。仅在缓解者中观察到肠道微生物组差异显著降低。随着治疗的进行,缓解者中伯克霍尔德菌-卡瓦列罗尼亚-副伯克霍尔德菌属和葡萄球菌属的相对丰度降低。此外,还观察到双歧杆菌属和多雷亚菌属的相对丰度增加。根据第8周的临床缓解情况,在预处理样本中按照相对丰度高低分布48个ASV,在受试者工作特征曲线上预测第8周的临床缓解,敏感性和特异性分别为72.4%和84.3%(曲线下面积为0.851)。

结论

在ADA治疗期间,肠道微生物群根据治疗反应发生多种变化。这些变化为预测对ADA的治疗反应提供了见解,并为UC提供了新的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d19/11346184/5406cb0ebf27/13099_2024_637_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d19/11346184/76df9025629e/13099_2024_637_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d19/11346184/5dfa212f7669/13099_2024_637_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d19/11346184/2c85334a65e7/13099_2024_637_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d19/11346184/a37eae1f91d3/13099_2024_637_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d19/11346184/5406cb0ebf27/13099_2024_637_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d19/11346184/76df9025629e/13099_2024_637_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d19/11346184/5dfa212f7669/13099_2024_637_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d19/11346184/2c85334a65e7/13099_2024_637_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d19/11346184/a37eae1f91d3/13099_2024_637_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d19/11346184/5406cb0ebf27/13099_2024_637_Fig5_HTML.jpg

相似文献

1
Dynamic changes in the gut microbiota composition during adalimumab therapy in patients with ulcerative colitis: implications for treatment response prediction and therapeutic targets.溃疡性结肠炎患者接受阿达木单抗治疗期间肠道微生物群组成的动态变化:对治疗反应预测和治疗靶点的意义
Gut Pathog. 2024 Aug 26;16(1):44. doi: 10.1186/s13099-024-00637-5.
2
Mucosal microbiota and gene expression are associated with long-term remission after discontinuation of adalimumab in ulcerative colitis.黏膜微生物群和基因表达与溃疡性结肠炎患者停用阿达木单抗后的长期缓解相关。
Sci Rep. 2020 Nov 5;10(1):19186. doi: 10.1038/s41598-020-76175-2.
3
Anti-TNF therapy for ulcerative colitis in Brazil: a comparative real-world national retrospective multicentric study from the Brazilian study group of IBD (GEDIIB).巴西溃疡性结肠炎的抗 TNF 治疗:巴西炎症性肠病研究组(GEDIIB)的一项全国性回顾性真实世界比较多中心研究。
BMC Gastroenterol. 2022 May 29;22(1):268. doi: 10.1186/s12876-022-02341-7.
4
Banxia Xiexin decoction modulates gut microbiota and gut microbiota metabolism to alleviate DSS-induced ulcerative colitis.半夏泻心汤通过调节肠道微生物群及其代谢物缓解 DSS 诱导的溃疡性结肠炎。
J Ethnopharmacol. 2024 May 23;326:117990. doi: 10.1016/j.jep.2024.117990. Epub 2024 Feb 27.
5
Effectiveness of adalimumab for the treatment of ulcerative colitis in clinical practice: comparison between anti-tumour necrosis factor-naïve and non-naïve patients.阿达木单抗治疗溃疡性结肠炎的临床疗效:抗肿瘤坏死因子初治与非初治患者的比较。
J Gastroenterol. 2017 Jul;52(7):788-799. doi: 10.1007/s00535-016-1274-1. Epub 2016 Oct 8.
6
Impact of the Concomitant Use of Immunomodulator and a Lower Week 8 Partial Mayo Score on the Persistence of Adalimumab in Refractory Ulcerative Colitis.免疫调节剂的联合使用和第 8 周较低的部分 Mayo 评分对阿达木单抗治疗难治性溃疡性结肠炎的持续缓解的影响。
Intern Med. 2021 Dec 15;60(24):3849-3856. doi: 10.2169/internalmedicine.7279-21. Epub 2021 Jun 12.
7
Changes in fecal metabolic and lipidomic features by anti-TNF treatment and prediction of clinical remission in patients with ulcerative colitis.抗TNF治疗对溃疡性结肠炎患者粪便代谢和脂质组学特征的影响及临床缓解的预测
Therap Adv Gastroenterol. 2023 May 2;16:17562848231168199. doi: 10.1177/17562848231168199. eCollection 2023.
8
Gut Microbiota Composition in Long-Remission Ulcerative Colitis is Close to a Healthy Gut Microbiota.溃疡性结肠炎缓解期患者的肠道微生物组成与健康人群接近。
Inflamm Bowel Dis. 2023 Sep 1;29(9):1362-1369. doi: 10.1093/ibd/izad058.
9
Effects of Xylo-Oligosaccharide on the Gut Microbiota of Patients With Ulcerative Colitis in Clinical Remission.低聚木糖对临床缓解期溃疡性结肠炎患者肠道微生物群的影响
Front Nutr. 2021 Dec 28;8:778542. doi: 10.3389/fnut.2021.778542. eCollection 2021.
10
Disease Severity and Immune Activity Relate to Distinct Interkingdom Gut Microbiome States in Ethnically Distinct Ulcerative Colitis Patients.疾病严重程度和免疫活性与不同种族溃疡性结肠炎患者独特的跨物种肠道微生物群状态相关。
mBio. 2016 Aug 16;7(4):e01072-16. doi: 10.1128/mBio.01072-16.

引用本文的文献

1
Interplay of Gut Microbiota, Biologic Agents, and Postoperative Anastomotic Leakage in Inflammatory Bowel Disease: A Narrative Review.炎症性肠病中肠道微生物群、生物制剂与术后吻合口漏的相互作用:一项叙述性综述
Int J Mol Sci. 2025 Jul 22;26(15):7066. doi: 10.3390/ijms26157066.
2
Unveiling the gut-heart potential connection: microbiota's role in kawasaki disease and coronary artery lesions.揭示肠道与心脏的潜在联系:微生物群在川崎病和冠状动脉病变中的作用。
Front Cell Infect Microbiol. 2025 May 29;15:1560083. doi: 10.3389/fcimb.2025.1560083. eCollection 2025.

本文引用的文献

1
Composition and diverse differences of intestinal microbiota in ulcerative colitis patients.溃疡性结肠炎患者肠道微生物菌群的组成及多样性差异。
Front Cell Infect Microbiol. 2022 Aug 30;12:953962. doi: 10.3389/fcimb.2022.953962. eCollection 2022.
2
Compositional changes in fecal microbiota associated with clinical phenotypes and prognosis in Korean patients with inflammatory bowel disease.韩国炎症性肠病患者粪便微生物群的组成变化与临床表型及预后的关系
Intest Res. 2023 Jan;21(1):148-160. doi: 10.5217/ir.2021.00168. Epub 2022 Jun 14.
3
Clinical outcomes and predictors of response for adalimumab in patients with moderately to severely active ulcerative colitis: a KASID prospective multicenter cohort study.
中度至重度活动性溃疡性结肠炎患者使用阿达木单抗的临床结局及反应预测因素:一项KASID前瞻性多中心队列研究
Intest Res. 2022 Jul;20(3):350-360. doi: 10.5217/ir.2021.00049. Epub 2021 Jul 23.
4
Metabolism Characteristics of Lactic Acid Bacteria and the Expanding Applications in Food Industry.乳酸菌的代谢特性及其在食品工业中的拓展应用
Front Bioeng Biotechnol. 2021 May 12;9:612285. doi: 10.3389/fbioe.2021.612285. eCollection 2021.
5
Interactive Tree Of Life (iTOL) v5: an online tool for phylogenetic tree display and annotation.交互式生命树 (iTOL) v5:一个用于显示和注释系统发育树的在线工具。
Nucleic Acids Res. 2021 Jul 2;49(W1):W293-W296. doi: 10.1093/nar/gkab301.
6
Gut Microbiota and Related Metabolites Were Disturbed in Ulcerative Colitis and Partly Restored After Mesalamine Treatment.溃疡性结肠炎患者的肠道微生物群及相关代谢产物发生紊乱,美沙拉嗪治疗后部分恢复。
Front Pharmacol. 2021 Jan 18;11:620724. doi: 10.3389/fphar.2020.620724. eCollection 2020.
7
Gut microbiome diversity in acute severe colitis is distinct from mild to moderate ulcerative colitis.急性重症结肠炎的肠道微生物多样性与轻度至中度溃疡性结肠炎不同。
J Gastroenterol Hepatol. 2021 Mar;36(3):731-739. doi: 10.1111/jgh.15232. Epub 2020 Sep 14.
8
Reproducible, interactive, scalable and extensible microbiome data science using QIIME 2.使用QIIME 2进行可重复、交互式、可扩展和可延伸的微生物组数据科学研究。
Nat Biotechnol. 2019 Aug;37(8):852-857. doi: 10.1038/s41587-019-0209-9.
9
Metabolic Functions of Gut Microbes Associate With Efficacy of Tumor Necrosis Factor Antagonists in Patients With Inflammatory Bowel Diseases.肠道微生物的代谢功能与炎症性肠病患者肿瘤坏死因子拮抗剂的疗效相关。
Gastroenterology. 2019 Nov;157(5):1279-1292.e11. doi: 10.1053/j.gastro.2019.07.025. Epub 2019 Jul 18.
10
A 30-year Trend Analysis in the Epidemiology of Inflammatory Bowel Disease in the Songpa-Kangdong District of Seoul, Korea in 1986-2015.1986-2015 年韩国首尔松坡-姜洞地区炎症性肠病的 30 年流行病学趋势分析。
J Crohns Colitis. 2019 Oct 28;13(11):1410-1417. doi: 10.1093/ecco-jcc/jjz081.