The gut fungal and bacterial microbiota in pediatric patients with inflammatory bowel disease introduced to treatment with anti-tumor necrosis factor-α

被引:5
|
作者
Ventin-Holmberg, Rebecka [1 ]
Hoyhtya, Miikka [2 ]
Saqib, Schahzad [3 ]
Korpela, Katri [3 ]
Nikkonen, Anne [4 ,5 ]
Salonen, Anne [3 ]
de Vos, Willem M. [3 ,6 ]
Kolho, Kaija-Leena [1 ,3 ,4 ,5 ]
机构
[1] Univ Helsinki, Translat Immunol Res Program, Helsinki, Finland
[2] Tampere Univ, Fac Med & Hlth Technol, Tampere, Finland
[3] Univ Helsinki, Fac Med, Human Microbiome Res Program, Helsinki, Finland
[4] Univ Helsinki, Stenbackinkatu 11 Skidicum, Helsinki, Finland
[5] Univ Helsinki, Childrens Hosp, Helsinki Univ Hosp, Stenbackinkatu 11 Skidicum, Helsinki, Finland
[6] Wageningen Univ, Lab Microbiol, Wageningen, Netherlands
基金
欧盟地平线“2020”;
关键词
FECAL MICROBIOTA; CROHNS-DISEASE; CALPROTECTIN; INFLIXIMAB; CHILDREN; THERAPY; ASSOCIATIONS; SEARCH;
D O I
10.1038/s41598-022-10548-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Pediatric inflammatory bowel disease (PIBD) is a globally increasing chronic inflammatory disease associated with an imbalanced intestinal microbiota and treated with several treatment options, including anti-tumor necrosis factor alpha (TNF-alpha), such as infliximab (IFX). Up to half of the patients do not respond to the drug and there are no methods for response prediction. Our aim was to predict IFX response from the gut microbiota composition since this is largely unexplored in PIBD. The gut microbiota of 30 PIBD patients receiving IFX was studied by MiSeq sequencing targeting 16S and ITS region from fecal samples collected before IFX and two and six weeks after the start of treatment. The response to IFX induction was determined by fecal calprotectin value < 100 mu g/g at week six. The bacterial microbiota differed significantly between response groups, with higher relative abundance of butyrate-producing bacteria in responders compared to non-responders at baseline, validated by high predictive power (area under curve = 0.892) for baseline Ruminococcus and calprotectin. Additionally, non-responders had higher abundance of Candida, while responders had higher abundance of Saccharomyces at the end of the study. The gut microbiota composition in PIBD patients could predict response to IFX treatment in the future.
引用
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页数:11
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