EB1010, a putative Christensenellaceae-derived microbial peptide, exhibits anti-inflammatory activity and therapeutic potential in ulcerative colitis

studies demonstrated that oral administration effectively reversed inflammation in both trinitrobenzene sulfonic acid- (TNBS)-induced rat and DSS-induced mouse models of colitis. Caco-2 transport assays revealed minimal peptide permeability, consistent with pharmacokinetic (PK) data showing no plasma detection in orally treated rats, supporting a local intestinal mode of action. EB1010 was well tolerated in a 4-week rat toxicology study, with no adverse effect observed at doses up to 1.5 mg/kg/d by intravenous administration. These findings position EB1010 as a safe, locally acting, microbiota-derived peptide with potential therapeutic applications.

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Publication Details

Journal
Gut Microbes
Published
2026-04-25
DOI
https://doi.org/10.1080/19490976.2026.2662547
Primary Topic
Probiotics and Fermented Foods
Type
article
Field-Weighted Citation Impact
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article

EB1010, a putative Christensenellaceae-derived microbial peptide, exhibits anti-inflammatory activity and therapeutic potential in ulcerative colitis

Christophe Bonny, Cendrine Nicoletti, Antonietta Cultrone, Camille Baudesson de Chanville et al.
Gut Microbes
Probiotics and Fermented Foods
article

EB1010, a putative Christensenellaceae-derived microbial peptide, exhibits anti-inflammatory activity and therapeutic potential in ulcerative colitis

Christophe Bonny, Cendrine Nicoletti, Antonietta Cultrone, Camille Baudesson de Chanville, Camille Mailhac, Eric Di Pasquale, Souphalone Luangsay, Laurent Chêne, Francesco Strozzi, William Farin, Marc Maresca, Laureen Bardouillet, Grégoire Chevalier, Hélène Pfister, Jessica Quessel, Philippe Rinaudo, Valentine Thomas, Stephanie Blum, Hélène Pereira, Maria L. Orsini Delgado, Hélène Toussaint
article en

Abstract

studies demonstrated that oral administration effectively reversed inflammation in both trinitrobenzene sulfonic acid- (TNBS)-induced rat and DSS-induced mouse models of colitis. Caco-2 transport assays revealed minimal peptide permeability, consistent with pharmacokinetic (PK) data showing no plasma detection in orally treated rats, supporting a local intestinal mode of action. EB1010 was well tolerated in a 4-week rat toxicology study, with no adverse effect observed at doses up to 1.5 mg/kg/d by intravenous administration. These findings position EB1010 as a safe, locally acting, microbiota-derived peptide with potential therapeutic applications.

Gut MicrobesVol. 18(1)
Institut de Neurophysiopathologie (FR), Drug Discovery Laboratory (Norway) (NO), Centrale Méditerranée (FR), Nestlé (France) (FR)
Zero hunger
Openalex Percentile: Top 14%
Probiotics and Fermented Foods
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