普氏粪杆菌
失调
医学
转录组
临床终点
免疫学
不利影响
疾病
克罗恩病
微生物群
内科学
炎症性肠病
免疫
临床试验
先天免疫系统
胃肠病学
结肠炎
肠道菌群
炎症
随机对照试验
疫苗试验
溃疡性结肠炎
人体微生物群
下调和上调
ATG16L1
生物标志物
细胞因子
肠粘膜
益生菌
生物信息学
作者
Perle Guarino-Vignon,Edouard Louis,Hang‐Phuong Pham,Giovanna Orianne,Emma Tkacz,Loic Brot,Eolia Mazzetti,Delphine Sedda,Pauline Ruffié,Nathalie Rolhion,Geert D’Haens,Benjamin Hadida,Philippe Langella,Harry Sokol
标识
DOI:10.1038/s41467-026-72375-y
摘要
A marked decrease in Faecalibacterium prausnitzii is a hallmark of Crohn's disease (CD)-associated dysbiosis and predicts disease relapse. Here, we present the development and first-in-human evaluation of F. prausnitzii strain EXL01 for CD treatment. The EXL01-strain demonstrates anti-inflammatory effects in four models of colitis in rodents. A first-in-human, open-label, single-arm study of oral EXL01 was conducted in eight adult participants with mild to moderate CD, following corticosteroids-induced clinical response or remission. The primary endpoint was safety, and secondary endpoints included clinical, endoscopic, histological, molecular, and microbiome assessments. Exploratory endpoints included mucosa transcriptome and cytokine levels. EXL01 is well-tolerated with no treatment-related adverse events. Six participants completed the study; two discontinued treatment due to disease flare. While gut microbiota composition remains largely stable, transcriptomic analyses reveal distinct changes in ileal gene expression following EXL01 treatment, notably modulation of immune-related genes and upregulation of energy metabolism pathways. Compared to participants who remained in remission, those who flared show higher baseline systemic inflammation markers and innate immunity gene expression. These findings demonstrate that oral administration of EXL01 is feasible and well tolerated and establishes proof-of-concept for F. prausnitzii as a first-in-class live biotherapeutic for CD. ClinicalTrials.gov registration: NCT05542355.
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