DUOX2 activation drives bacterial translocation and subclinical inflammation in IBD-associated dysbiosis

Elevated DUOX2 signalling contributes to epithelial barrier dysfunction, microbiome alterations and subclinical inflammation. Butyrate and HDAC inhibitors reversed these effects, indicating that DUOX2 may be a therapeutic target in IBD.

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Publication Details

Journal
Gut
Published
2025-04-29
DOI
https://doi.org/10.1136/gutjnl-2024-334346
Citations
18
Primary Topic
Gut microbiota and health
Type
article
Field-Weighted Citation Impact
14.51

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article

DUOX2 activation drives bacterial translocation and subclinical inflammation in IBD-associated dysbiosis

Siobhan Proksell, Fahong Yu, David H. Kerman, María T. Abreu et al.
18 citations
Gut
Gut microbiota and health
14.51
article

DUOX2 activation drives bacterial translocation and subclinical inflammation in IBD-associated dysbiosis

Siobhan Proksell, Fahong Yu, David H. Kerman, María T. Abreu, Irina Fernández, Maria A. Quintero, Hajar Hazime, Katerina M. Faust, Eddy E. Gonzalez-Horta, Judith Pignac-Kobinger, Amar R. Deshpande, Gloria Michelle Ducasa, Christian Jobin, Oriana M. Damas, Nivis Brito, Juan F. Burgueño, Landon Wilson, Raad Z. Gharaibeh, Ana M. Santander, Stephen Barnes, Yanping Zhang
article en
18 citations

Abstract

Elevated DUOX2 signalling contributes to epithelial barrier dysfunction, microbiome alterations and subclinical inflammation. Butyrate and HDAC inhibitors reversed these effects, indicating that DUOX2 may be a therapeutic target in IBD.

GutVol. 74(10)
Cedars-Sinai Medical Center (US), University of Miami (US), University of Alabama at Birmingham (US), University of Florida (US)
National Institute of Diabetes and Digestive and Kidney Diseases
Good health and well-being
Openalex Percentile: Top 1%
Gut microbiota and health
14.51
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