医疗保健
炎症
精密医学
医学
内科学
政治学
病理
法学
作者
Huan Zhang,B. J. Yang Lee,Tong Wang,Xuesong Xiang,Yafang Tan,Yanping Han,Yujing Bi,Fachao Zhi,Xin Wang,Fang He,Seppo Salminen,Baoli Zhu,Ruifu Yang
标识
DOI:10.1016/j.hlife.2025.04.004
摘要
The terms “inflammatome” (holistic inflammation networks) and “inflammatomics” (a novel omics field) were proposed to decode dysbiosis-driven chronic inflammation and its disease links. Inflammatomics explores microbiota–immune crosstalk, particularly innate immune interactions, revealing how dysregulated microbial communities trigger chronic inflammation underlying disorders like inflammatory bowel disease, metabolic diseases, and neurodegeneration. This discipline transcends traditional inflammation paradigms by dissecting molecular pathways connecting dysbiosis to systemic inflammation, enabling early detection and precision interventions. It integrates evolutionary perspectives on host–microbe interactions, emphasizing the human body as a stress-sensitive “organ”. Challenges include standardizing inflammatome profiling, translating findings into clinical tools, and advancing multiomics technologies. By bridging microbial ecology, immunology, and systems medicine, inflammatomics holds a transformative potential to shift health care from reactive treatment to proactive, personalized prevention, targeting disease origins shaped by chronic inflammatome dysregulation.
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