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原发性胆汁酸塑造炎症性肠病相关原发性硬化性胆管炎中的外周免疫。

Primary bile acid shapes peripheral immunity in inflammatory bowel disease-associated primary sclerosing cholangitis.

作者信息

Santos André A, Pires David, Marques Vanda, Alesina Nicole, Herraez Elisa, Roudnický Pavel, Rodrigues Pedro M, Godinho-Santos Ana, Bravo Ana Catarina, Gouveia Catarina, Saraiva Susana, Correia Luís, Crespo Ricardo, da Silva João Pereira, Cravo Marília, Potesil David, Zdráhal Zbyněk, Banales Jesus Maria, Marin Jose J G, Torres Joana, Rodrigues Cecília Maria Pereira

机构信息

Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Lisboa, Portugal.

CIIS - Centro de Investigação Interdisciplinar em Saúde, Faculdade de Medicina, Universidade Católica Portuguesa, Lisboa, Portugal.

出版信息

Clin Sci (Lond). 2025 Jun 26;138(12):703-716. doi: 10.1042/CS20256078.

Abstract

Primary sclerosing cholangitis (PSC) is a chronic cholestatic liver disease often associated with underlying inflammatory bowel disease (IBD). This study investigates how PSC predisposes individuals to altered inflammatory immune responses compared with IBD alone. A case-control study was conducted with a cohort of 75 patients, including 16 with PSC (14 with concomitant IBD), 39 with IBD alone, and 20 controls. Serum bile acid profile, proteomic analysis, and immune-related gene expression in the colon tissue were examined. Colonic tissue from PSC patients exhibited up-regulation of immune regulation and inflammatory signaling mRNA markers, including LGR5, IL-8, CCL2, COX2, TWIST1, and SNAIL. Additionally, PSC patients displayed a distinct proinflammatory serum proteomic signature and moderate elevation of some bile acids, such as glycochenodeoxycholic acid (GCDCA). Co-incubation of human-derived monocytes with GCDCA partially replicated the inflammatory profile observed in PSC. These findings suggest that circulating bile acids modulate the peripheral immune system proinflammatory response, contributing to the unique PSC phenotype.

摘要

原发性硬化性胆管炎(PSC)是一种慢性胆汁淤积性肝病,常与潜在的炎症性肠病(IBD)相关。本研究调查了与单独的IBD相比,PSC如何使个体易发生改变的炎症免疫反应。进行了一项病例对照研究,纳入了75名患者,包括16名PSC患者(14名合并IBD)、39名单独患有IBD的患者和20名对照。检测了血清胆汁酸谱、蛋白质组分析以及结肠组织中的免疫相关基因表达。PSC患者的结肠组织表现出免疫调节和炎症信号mRNA标志物的上调,包括LGR5、IL-8、CCL2、COX2、TWIST1和SNAIL。此外,PSC患者表现出独特的促炎血清蛋白质组特征以及一些胆汁酸(如甘氨鹅脱氧胆酸(GCDCA))的中度升高。人源单核细胞与GCDCA共同孵育部分复制了PSC中观察到的炎症特征。这些发现表明,循环胆汁酸调节外周免疫系统的促炎反应,促成了独特的PSC表型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2ca/12312387/2f3a3b1b24c3/CS-139-12-CS20256078-g001.jpg

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