炎症体
先天免疫系统
下调和上调
干扰素
脂多糖
肿瘤坏死因子α
细胞因子
巨噬细胞
免疫学
分子生物学
体外
微生物学
炎症
生物
免疫系统
生物化学
基因
作者
Michael Rooney,Shivalee Duduskar,Mohamed Ghait,Johanna Reißing,Sven Stengel,Philipp A. Reuken,Stefanie Quickert,Alexander Zipprich,Michael Bauer,Ashley J. Russo,Vijay Rathinam,Andreas Stallmach,Ignacio Rubio,Tony Bruns
标识
DOI:10.1016/j.jhep.2024.06.019
摘要
Patients with cirrhosis exhibit impaired immune responses and increased susceptibility to bacterial infections. This study reveals that type-I interferon responses, triggered by pathogen-associated molecular patterns, are crucial in regulating macrophage activation and priming them for inflammatory responses. Additionally, we elucidate the mechanisms by which type-I interferons promote the release of progranulin from macrophages during spontaneous bacterial peritonitis. Our findings enhance understanding of how bacterial translocation affects immune responses, identify novel biomarkers for inflammasome activation during infections, and point to potential therapeutic targets.
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