儿科克罗恩病患者接受抗肿瘤坏死因子治疗后,粪便细菌组和代谢组图谱与黏膜炎症活动减少有关。

IF 8.3 2区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Jakub Hurych, Anna Mascellani Bergo, Tereza Lerchova, Lucie Hlinakova, Michal Kubat, Hana Malcova, Dita Cebecauerova, Jan Schwarz, Eva Karaskova, Tomas Hecht, Radim Vyhnanek, Lenka Toukalkova, Vojtech Dotlacil, Katerina Greinerova, Anabela Cizkova, Rudolf Horvath, Jiri Bronsky, Jaroslav Havlik, Ondrej Hradsky, Ondrej Cinek
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引用次数: 0

摘要

背景和目的:使用抗肿瘤坏死因子α抗体[anti-TNF]治疗可改变克罗恩病[CD]患者粪便菌群失调的情况。然而,这些变化是否是由于粘膜炎症活动减少所致,或者在肠道健康的受试者中是否也可能观察到类似的细菌群反应,目前尚不清楚。因此,我们探讨了 CD 儿童服用抗肿瘤坏死因子后粪便细菌组和代谢组的变化[及治疗反应],并将其与服用抗肿瘤坏死因子的幼年特发性关节炎[JIA]儿童进行对比:方法:通过16S rDNA[V4区]大规模平行测序分析细菌组,通过1H核磁共振成像分析粪便代谢组。治疗开始 3 个月后,通过 MINI 指数评估了粘膜愈合对治疗的反应。我们还测试了英夫利昔单抗对几种代表性肠道细菌菌株体外生长的抑制作用:我们分析了 121 名儿童(CD 54 名,JIA 18 名,健康 49 名)的 530 份粪便样本。抗肿瘤坏死因子会改变 CD 患者的细菌群落组成:抗肿瘤坏死因子会增加梭状芽孢杆菌中的三个成员,而类杆菌则会减少。在粪便代谢物中,葡萄糖和甘油增加,而异亮氨酸和尿嘧啶减少。其中一些变化因抗 TNF 后的治疗反应[粘膜愈合]而不同。在 JIA 抗肿瘤坏死因子治疗后,细菌组或代谢组没有发生明显变化。在盘扩散试验中,英夫利西单抗对细菌生长没有影响:我们的研究结果表明,在 CD 中观察到的细菌组和代谢组变化是肠道粘膜愈合造成的,而不是抗肿瘤坏死因子的普遍影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Faecal Bacteriome and Metabolome Profiles Associated with Decreased Mucosal Inflammatory Activity Upon Anti-TNF Therapy in Paediatric Crohn's Disease.

Background and aims: Treatment with anti-tumour necrosis factor α antibodies [anti-TNF] changes the dysbiotic faecal bacteriome in Crohn's disease [CD]. However, it is not known whether these changes are due to decreasing mucosal inflammatory activity or whether similar bacteriome reactions might be observed in gut-healthy subjects. Therefore, we explored changes in the faecal bacteriome and metabolome upon anti-TNF administration [and therapeutic response] in children with CD and contrasted those to anti-TNF-treated children with juvenile idiopathic arthritis [JIA].

Methods: Faecal samples collected longitudinally before and during anti-TNF therapy were analysed with regard to the bacteriome by massively parallel sequencing of the 16S rDNA [V4 region] and the faecal metabolome by 1H nuclear magnetic resonance imaging. The response to treatment by mucosal healing was assessed by the MINI index at 3 months after the treatment started. We also tested several representative gut bacterial strains for in vitro growth inhibition by infliximab.

Results: We analysed 530 stool samples from 121 children [CD 54, JIA 18, healthy 49]. Bacterial community composition changed on anti-TNF in CD: three members of the class Clostridia increased on anti-TNF, whereas the class Bacteroidia decreased. Among faecal metabolites, glucose and glycerol increased, whereas isoleucine and uracil decreased. Some of these changes differed by treatment response [mucosal healing] after anti-TNF. No significant changes in the bacteriome or metabolome were noted upon anti-TNF in JIA. Bacterial growth was not affected by infliximab in a disc diffusion test.

Conclusions: Our findings suggest that gut mucosal healing is responsible for the bacteriome and metabolome changes observed in CD, rather than any general effect of anti-TNF.

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来源期刊
Journal of Crohns & Colitis
Journal of Crohns & Colitis 医学-胃肠肝病学
CiteScore
15.50
自引率
7.50%
发文量
1048
审稿时长
1 months
期刊介绍: Journal of Crohns and Colitis is concerned with the dissemination of knowledge on clinical, basic science and innovative methods related to inflammatory bowel diseases. The journal publishes original articles, review papers, editorials, leading articles, viewpoints, case reports, innovative methods and letters to the editor.
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